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benzoic acid

Creu erthygl

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chemical compound

Adnoddau allanol

CSD Refcode
BENZAC01[1]
BENZAC02[1]
ZVG number
22810
dynodwr HCIS
433
dynodwr MeSH
D019817[2]

enwyd fel: Benzoic Acid

dynodwr Encyclopædia Britannica Online
science/benzoic-acid

enwyd fel: benzoic acid

ChEMBL ID
CHEMBL541[3]
Natural Product Atlas ID
NPA008069[4][5]
Nikkaji ID
J2.358B
dynodwr ICSC
0103
rhif E
E210
Open Food Facts food additive ID
e210-benzoic-acid
Cod MeSH
D02.241.223.100.120
D02.455.426.559.389.127.117
Great Russian Encyclopedia Online ID (old version)
UNII
8SKN0B0MIM[6][5]
rhif RTECS
DG0875000
ECHA Substance Infocard ID
100.000.562[7]
UM-BBD compound ID
c0121
PDB structure ID
5DNV[8]
1GYX[9]
3R76[10]
3R75[11]
3IT4[12]
1TMX[13]
4ZJZ[14]
4M51[15]
3FFP[16]
1KQB[17]
2V2G[18]
5E4D[19]
1REF[20]
1RED[21]
2V7B[22]
1GXS[23]
1RU9[24]
1RUA[25]
1RUL[26]
1RUM[27]
1RUK[28]
1RUP[29]
2Q9R[30]
5DNU[31]
5IM2[32]
1UUJ[33]
1VE9[34]
2M9P[35]
2M9Q[36]
2VJ1[37]
2AJY[38]
4HZ2[39]
1NCW[40]
4EAT[41]
2Q38[42]
3RHG[43]
1OC3[44]
3F8E[45]
1YAJ[46]
2O02[47]
1WSP[48]
2V32[49]
3FBW[50]
1W9Q[51]
1W9O[52]
1W9E[53]
2VL2[54]
5EXA[55]
4F5Z[56]
1I7Q[57]
3TGV[58]
1V1T[59]
3CCF[60]
4UTN[61]
4UTX[62]
3GV1[63]
2OK6[64]
4PBH[65]
2Q0J[66]
2Q0I[67]
4IJI[68]
3HGI[69]
1URM[70]
2F8D[71]
1HZ4[72]
1KIF[73]
1I69[74]
1A8U[75]
4UTZ[76]
4UTR[77]
4UTV[78]
1JU4[79]
2AK1[80]
4XDQ[81]
4ZGF[82]
2QL8[83]
4UU8[84]
3TX2[85]
4MF6[86]
3R9T[87]
3R9S[88]
3V7P[89]
1HD2[90]
2RHM[91]
1L7Q[92]
2F7A[93]
2F78[94]
2DU8[95]
2V41[96]
4OU1[97]
1ONI[98]
1HKQ[99]
3V1N[100]
4ZVC[101]
4UU7[102]
4EVR[103]
4UUB[104]
4UUA[105]
1S9A[106]
1REE[107]
1H4O[108]
1OP3[109]
3O9M[110]
5FXF[111]
2QMQ[112]
2Q6U[113]
2FP7[114]
5EWZ[115]
1UKB[116]
3S46[117]
5DZK[118]
2Q1B[119]
3IEO[120]
3U1I[121]
5DQY[122]
5EM1[123]
1DJR[124]
1S8F[125]
DSSTox substance ID
DTXSID6020143[126][5]
DrugCentral ID
4664[127]
CAMEO Chemicals ID
2585
CCDC Number
1108733[1]
1108734[1]
Encyclopedia of China (Third Edition) ID
157428
Australian Educational Vocabulary ID
scot/9566
National Library of Israel J9U ID
987007566441405171[128]
NDF-RT
N0000146160[6]
dynodwr Freebase
/m/01bbg[129]
Probes And Drugs ID
PD001113
dynodwr Microsoft Academic
2778844314
dynodwr LCAuth
sh2003009190[130]

enwyd fel: Benzoic acid

PubChem CID
243[131][5]
20144841[5]
GND
4144531-4
Gmelin number
2946
NSC number
149
758203
dynodwr Quora
Benzoic-Acid-1[132]
dynodwr YSO
18984[133]

enwyd fel: bentsoehappo, bensoesyra, benzoic acid

dynodwr yn thesawrws y BNCF
32771[134]
SPLASH
splash10-0a6r-9600000000-d08dbc757a6de6c3f54e
splash10-0adi-9800000000-40f904bf20072c72a08b
splash10-0pk9-9800000000-b93fc1120a1c74b88fa3
splash10-05i0-5900000000-1b6bbf98557af374f3a5
splash10-0570-0900000000-ecd208f1e7b4d5ad85f2
splash10-00di-0900000000-4644ee08861e75d0b808
splash10-00b9-9400000000-11baabb3c0bb283b1c6e
splash10-004l-9100000000-4875643627420279223b
splash10-0006-9000000000-97a21f3206f5c1f0ba7e
splash10-0a70-0900000000-5284a0c1c77a1979e1f4
splash10-00di-0900000000-05e037a449f9df7f6d42
splash10-0a70-0900000000-cec9e1ab69521049d1e4
splash10-00di-0900000000-ffdcca5bd2b965040c67
splash10-0pk9-8900000000-3d79c70c455799ab33e3
splash10-00b9-9400000000-29ca905567aa5c59d46b
splash10-004i-9100000000-dafd91c9134bc4143743
splash10-00b9-9500000000-f312a552bef1a2927e64
splash10-056r-3900000000-1c74c32fa650fcd4cb4d
splash10-05di-9700000000-ff2b00d52402533f7499
dynodwr KEGG
D00038[135]
C00180
Reaxys registry number
636131[135]
OpenAlex ID
C2778844314[136]
dynodwr HMDB
HMDB0001870[4][5]
dynodwr KBpedia
BenzoicAcid[137]
CAB ID
60363[138]
InChIKey
WPYMKLBDIGXBTP-UHFFFAOYSA-N[131][139]
Cannabis Database ID
004927[140]
Dynodwr Drugbank (Alberta)
DB03793[5]
ID NALT
16657
ChEBI ID
30746[3][141][142]

mapping relation type: exact match

InChI
InChI=1S/C7H6O2/c8-7(9)6-4-2-1-3-5-6/h1-5H,(H,8,9)[131]
CosIng number
32134[143]
J-GLOBAL ID
200907041563325370
SureChEMBL ID
SCHEMBL1378[4][5]
PDB Ligand
BEZ
Store norske leksikon ID
benzosyre
Den Store Danske ID
benzoesyre
AICS Chemical ID (BEING DELETED)
732
IEDB Epitope ID
139965[144]
DSSTOX compound identifier
DTXCID80143
KNApSAcK ID
C00000207[135][4][5]
UMLS CUI
C0053225[6]
JECFA number
850[145]
Rhif Cofrestru CAS
65-85-0[6]
FL number
08.021[146]
ChemSpider ID
238[147]
EC number
200-618-2[6]
NMRShiftDB structure ID
10022010[5]
PesticideInfo chemical ID
PRI1584
MassBank accession ID
MSBNK-Fac_Eng_Univ_Tokyo-JP003197
MSBNK-Fac_Eng_Univ_Tokyo-JP009208
MSBNK-BGC_Munich-RP012801
MSBNK-BGC_Munich-RP012802
MSBNK-BGC_Munich-RP012803
MSBNK-BGC_Munich-RP012811
MSBNK-Fac_Eng_Univ_Tokyo-JP003534
MSBNK-Fac_Eng_Univ_Tokyo-JP011225
MSBNK-Osaka_Univ-OUF00127
MSBNK-Fac_Eng_Univ_Tokyo-JP004285
MSBNK-GL_Sciences_Inc-GLS00149
MSBNK-Keio_Univ-KO000319
MSBNK-Keio_Univ-KO000320
MSBNK-Keio_Univ-KO000321
MSBNK-Keio_Univ-KO000322
Great Russian Encyclopedia portal ID
benzoinaia-kislota-015ef7
RxNorm ID
18989[6]
dynodwr HSDB
704[148]

enghraifft o'r canlynol

math o endid cemegol

isddosbarth o'r canlynol

benzoic acid

rhan o'r canlynol

cellular response to benzoic acid[149]

rôl y pwnc: reactant

response to benzoic acid[149]

rôl y pwnc: reactant

defnydd

cyffur meddygol[150]
food preservative[151][152]

adeiledd gemegol

màs

122.036779432 uned Dalton[153]

conjugate base

benzoate

fformwla gemegol

C₇H₆O₂[131]

SMILES

C1=CC=C(C=C1)C(=O)O[131]

ionization energy

9.47 electronvolt[154]

specific heat capacity

102.7 joule per mole kelvin[155]

tymheredd: 200 Kelvin

cyflwr mater: solid

123.5 joule per mole kelvin[155]

tymheredd: 250 Kelvin

cyflwr mater: solid

147.4 joule per mole kelvin[155]

tymheredd: 300 Kelvin

cyflwr mater: solid

172 joule per mole kelvin[155]

tymheredd: 350 Kelvin

cyflwr mater: solid

dwysedd

1.2659 gram per cubic centimetre[156]

tymheredd: 15 gradd Celsius

cyflwr mater: solid

ymdoddbwynt

122.34±0.005 gradd Celsius[156]

uncertainty corresponds to: expanded uncertainty

boiling point

250.2±0.6 gradd Celsius[156]

under pressure: 101,325 pascal

uncertainty corresponds to: expanded uncertainty

solubility

2.7 gram per litre[157]

solvent: dŵr

tymheredd: 20 gradd Celsius

2.09 gram per kilogram[158]

solvent: dŵr

tymheredd: 10 gradd Celsius

3.44 gram per kilogram[158]

solvent: dŵr

tymheredd: 25 gradd Celsius

8.49 gram per kilogram[158]

solvent: dŵr

tymheredd: 50 gradd Celsius

partition coefficient water/octanol

1.88[159]

tymheredd: 25 gradd Celsius

pKa

4.204[160]

tymheredd: 25 gradd Celsius

solvent: dŵr

refractive index

1.504[156]

tymheredd: 132 gradd Celsius

wavelength: 589 nanomedr

flash point

121 gradd Celsius[157][161]

dull penderfynu: Pensky–Martens closed-cup test

autoignition temperature

570 gradd Celsius[161]

safety classification and labelling

NFPA 704: Standard System for the Identification of the Hazards of Materials for Emergency Response

NFPA Health: 2

NFPA Special: dim gwerth

NFPA Fire: 1

NFPA Instability: 0

found in taxon

Streptomyces lavendulae[162]
Llwyn Cwrens Duon[163]
Poplysen ddu[164]
Ephedra equisetina[165]
Hoya australis[166]
Hoya bandaensis[166]
Hoya cinnamomifolia[166]
Hoya coronaria[166]
Hoya diversifolia[166]
Hoya crassipes[166]
Hoya fraterna[166]
Hoya obovata[166]
Hoya pseudolanceolata[166]
Hoya shepherdii[166]
Hoya longifolia[166]
Hoya latifolia[166]
Hoya macrophylla[166]
Hoya bella[166]
Hoya multiflora[166]
Hoya imperialis[166]
Hoya lacunosa[166]
Osmorhiza aristata[167]
Bricyllwydden[168]
Coeden eirin gwlanog[168]
Draenen Ddu[169]
Llygad y dydd[170]
Populus tomentosa[171]
Populus tremuloides[171][172]
Bysedd-y-blaidd culddail[173]
Plumeria rubra[174]
Populus laurifolia[175][176]
Populus violascens[177]
Polygala senega[178]
Gwylys[179]
Lactobacillus plantarum[180]
Senecio viscosissimus[181]
Senecio adenotrichius[181]
Llygaeren America[182][183][184][185][186][187][188][189][190][191][192]
Populus lasiocarpa[193]
Scutellaria baicalensis[194]
Populus deltoides[195][196]
Populus euphratica[197]
Basella alba[198]
Populus grandidentata[172][199]
Posidonia oceanica[200]
Ciwcymbr[201]
Malus pumila[202]
Paeonia veitchii[203]
Mangifera indica[204][205][206]
Llusen goch[184][207][208]
Pinwydden gochfrig[209]
Senna obtusifolia[210]
Hoffmannia strigillosa[211]
Pavonia alba[212]
Y bengaled arw[213][214]
Melodorum fruticosum[215]
Ffeuen Ffrengig[216][217]
Llydan y ffordd[218][219]
Llysiau lliw[220][221]
Cinnamomum kotoense[222]
Homalium cochinchinensis[223][224]
Diplostephium ericoides[225]
Oxytropis trichophysa[226]
Phycomyces blakesleeanus[227]
Gardenia coronaria[228]
Rorippa indica[229]
Gardenia sootepensis[230]
Uvaria mocoli[231]
Aristolochia heterophylla[232]
Aristolochia foveolata[233]
Paeonia obovata[234]
Crocus sativus[235][236]
Acremonium[237][238]
Taraxacum formosanum[239][240]
Onosma hispida[241][242]
Paeonia emodi[243]
Cryptocarya amygdalina[244]
Gynura japonica[245]
Begonia nantoensis[246][247]
Hibiscus taiwanensis[248][249]
Wystrysen y coed[250]
Marchrawnen yr ardir[251]
Hohenbuehelia serotina[252]
Aconitum japonicum[253]
Desmos chinensis[254]
Securidaca inappendiculata[255]
Pertya glabrescens[256]
Pulicaria angustifolia[257]
Pinus densiflora[258]
Baco[259]
Pinus pumila[260]
Burchardia multiflora[261]
Colchicum kurdicum[262]
Colchicum manissadjianii[262]
Colchicum soboliferum[262]
Centaurea collina[263]
Ifloga spicata[264]
Hypoestes triflora[265]
Bellardia trixago[266]
Nassauvia revoluta[267]
strawberries[268]
Pelargonium graveolens[269]
Dail y beiblau[270]
Stachylidium[271]
alpenrose[272]
Paeonia rockii[273][274][275][276][277]
Chlamydomonas reinhardtii[278]
Streptomyces ambofaciens[279][280]
Morgrugyn[281]
Catharanthus roseus[282]
Lemna aequinoctialis[283][284]
afocado[285]
Petiveria alliacea[286]
Rhedynen ungoes[287][288]
Meillionen waetgoch[289]
Ewcalyptws[290]
Hoya ovalifolia[166]
Iris[291]
Cacao[292]
Abies nephrolepis[293]
Alnus pendula[294]
Aloe ferox[295]
Bedwen arian[296]
Melicope semecarpifolia[297]
Paenibacillus polymyxa[298]
Pteris ensiformis[299]
Tabernaemontana divaricata[300]
Homo sapiens[301][302]
Murraya paniculata[303]
Hydnocarpus annamensis[304]
Viola hondoensis[305]
Uvaria angolensis[231]
Momordica charantia[306]
Chamaecyparis formosensis[307]
Poplysen wen[171][308]
Paeonia anomala[309]
Merendera sobolifera[262]
Rhaponticum carthamoides[310]
Populus candicans[308]
Lemna perpusilla[284]
Adenostoma sparsifolium[311][312]
Paeonia peregrina[275]
Caenorhabditis elegans[313]
Piper sarmentosum[314]
Tripterygium wilfordii[315]
Coeden geirios du[316]
Blodyn yr haul[317]
Carica papaya[318]
Sbigoglys[319]
Bysedd-y-blaidd gwyn[320]
Pysen[321]
Grawnafal[322]
Sbriwsen Norwy[323]
Tomato[324][325]
Vaccinium[326][327]
Osmanthus fragrans[328]
indrawn[329]
Eutrema japonicum[330]
Aristolochia kaempferi[232][331]
Poplysen falmaidd y Dwyrain[308]
Taraxacum mongolicum[239][240]
Paeonia lactiflora[332][333][203][334][335][336]
Paeonia tenuifolia[274]
Paeonia suffruticosa[337]
Ascochyta medicaginicola[338]
Populus szechuanica[177]
Prunus africana[339][340]
pomelo[209]
Citrus grandis[209]
Citrus medica[209]
Aethnen[341][171]
Escherichia coli[342]
Hoya tsangii[166]
Adenostoma fasciculatum[312]
Sarcomyxa serotina[252]
Malus domestica[202]

disgrifiwyd gan y ffynhonnell

Encyclopædia Britannica 11th edition

mae'r datganiad yn destun o: 1911 Encyclopædia Britannica/Benzoic Acid

Great Soviet Encyclopedia (1926–1947)

mae'r datganiad yn destun o: Q43454615

rôl y pwnc

Antifungal[152]
llenwydd
primary metabolite[343]

MCN code

2916.31.10

yn cynnwys

ocsigen
carbon
hydrogen

yn wahanol i

benzoic acid

categori Comin

Benzoic acid

Cyfeiriadau

  1. ↑ 1.0 1.1 1.2 1.3 Cambridge Structural Database, 10 Ionawr 2023, InChIKey match
  2. ↑ Mesh ID, 14 Mawrth 2018, D019817
  3. ↑ 3.0 3.1 ChEMBL, 19 Tachwedd 2016, Saesneg, BENZOIC ACID, CHEMBL541
  4. ↑ 4.0 4.1 4.2 4.3 inferred from InChIKey
  5. ↑ 5.00 5.01 5.02 5.03 5.04 5.05 5.06 5.07 5.08 5.09 WPYMKLBDIGXBTP-UHFFFAOYSA-N, InChIKey
  6. ↑ 6.0 6.1 6.2 6.3 6.4 6.5 Global Substance Registration System, 19 Tachwedd 2016, Saesneg, benzoic acid, 8SKN0B0MIM
  7. ↑ ECHA Substance Infocard database, 27 Rhagfyr 2018, 100.000.562, Benzoic acid, CAS no.: 65-85-0
  8. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 5DNV, 5DNV
  9. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 1GYX, 1GYX
  10. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 3R76, 3R76
  11. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 3R75, 3R75
  12. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 3IT4, 3IT4
  13. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 1TMX, 1TMX
  14. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 4ZJZ, 4ZJZ
  15. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 4M51, 4M51
  16. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 3FFP, 3FFP
  17. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 1KQB, 1KQB
  18. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 2V2G, 2V2G
  19. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 5E4D, 5E4D
  20. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 1REF, 1REF
  21. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 1RED, 1RED
  22. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 2V7B, 2V7B
  23. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 1GXS, 1GXS
  24. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 1RU9, 1RU9
  25. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 1RUA, 1RUA
  26. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 1RUL, 1RUL
  27. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 1RUM, 1RUM
  28. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 1RUK, 1RUK
  29. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 1RUP, 1RUP
  30. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 2Q9R, 2Q9R
  31. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 5DNU, 5DNU
  32. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 5IM2, 5IM2
  33. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 1UUJ, 1UUJ
  34. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 1VE9, 1VE9
  35. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 2M9P, 2M9P
  36. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 2M9Q, 2M9Q
  37. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 2VJ1, 2VJ1
  38. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 2AJY, 2AJY
  39. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 4HZ2, 4HZ2
  40. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 1NCW, 1NCW
  41. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 4EAT, 4EAT
  42. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 2Q38, 2Q38
  43. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 3RHG, 3RHG
  44. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 1OC3, 1OC3
  45. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 3F8E, 3F8E
  46. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 1YAJ, 1YAJ
  47. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 2O02, 2O02
  48. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 1WSP, 1WSP
  49. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 2V32, 2V32
  50. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 3FBW, 3FBW
  51. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 1W9Q, 1W9Q
  52. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 1W9O, 1W9O
  53. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 1W9E, 1W9E
  54. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 2VL2, 2VL2
  55. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 5EXA, 5EXA
  56. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 4F5Z, 4F5Z
  57. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 1I7Q, 1I7Q
  58. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 3TGV, 3TGV
  59. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 1V1T, 1V1T
  60. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 3CCF, 3CCF
  61. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 4UTN, 4UTN
  62. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 4UTX, 4UTX
  63. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 3GV1, 3GV1
  64. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 2OK6, 2OK6
  65. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 4PBH, 4PBH
  66. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 2Q0J, 2Q0J
  67. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 2Q0I, 2Q0I
  68. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 4IJI, 4IJI
  69. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 3HGI, 3HGI
  70. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 1URM, 1URM
  71. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 2F8D, 2F8D
  72. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 1HZ4, 1HZ4
  73. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 1KIF, 1KIF
  74. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 1I69, 1I69
  75. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 1A8U, 1A8U
  76. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 4UTZ, 4UTZ
  77. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 4UTR, 4UTR
  78. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 4UTV, 4UTV
  79. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 1JU4, 1JU4
  80. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 2AK1, 2AK1
  81. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 4XDQ, 4XDQ
  82. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 4ZGF, 4ZGF
  83. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 2QL8, 2QL8
  84. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 4UU8, 4UU8
  85. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 3TX2, 3TX2
  86. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 4MF6, 4MF6
  87. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 3R9T, 3R9T
  88. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 3R9S, 3R9S
  89. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 3V7P, 3V7P
  90. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 1HD2, 1HD2
  91. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 2RHM, 2RHM
  92. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 1L7Q, 1L7Q
  93. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 2F7A, 2F7A
  94. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 2F78, 2F78
  95. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 2DU8, 2DU8
  96. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 2V41, 2V41
  97. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 4OU1, 4OU1
  98. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 1ONI, 1ONI
  99. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 1HKQ, 1HKQ
  100. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 3V1N, 3V1N
  101. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 4ZVC, 4ZVC
  102. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 4UU7, 4UU7
  103. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 4EVR, 4EVR
  104. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 4UUB, 4UUB
  105. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 4UUA, 4UUA
  106. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 1S9A, 1S9A
  107. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 1REE, 1REE
  108. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 1H4O, 1H4O
  109. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 1OP3, 1OP3
  110. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 3O9M, 3O9M
  111. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 5FXF, 5FXF
  112. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 2QMQ, 2QMQ
  113. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 2Q6U, 2Q6U
  114. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 2FP7, 2FP7
  115. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 5EWZ, 5EWZ
  116. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 1UKB, 1UKB
  117. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 3S46, 3S46
  118. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 5DZK, 5DZK
  119. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 2Q1B, 2Q1B
  120. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 3IEO, 3IEO
  121. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 3U1I, 3U1I
  122. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 5DQY, 5DQY
  123. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 5EM1, 5EM1
  124. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 1DJR, 1DJR
  125. ↑ Protein Data Bank, 19 Hydref 2016, Saesneg, 1S8F, 1S8F
  126. ↑ Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard
  127. ↑ UniChem
  128. ↑ Llyfrgell Genedlaethol Israel
  129. ↑ Freebase Data Dumps, 28 Hydref 2013
  130. ↑ Nuovo soggettario, https://thes.bncf.firenze.sbn.it/termine.php?id=32771, 15 Mehefin 2021
  131. ↑ 131.0 131.1 131.2 131.3 131.4 PubChem, 19 Tachwedd 2016, Saesneg, 243, benzoic acid
  132. ↑ Quora
  133. ↑ YSO-Wikidata mapping project, 28 Ionawr 2022
  134. ↑ National Central Library of Florence
  135. ↑ 135.0 135.1 135.2 ChEBI, 19 Hydref 2016, Saesneg, benzoic acid, 30746
  136. ↑ OpenAlex, 26 Ionawr 2022, https://docs.openalex.org/download-snapshot/snapshot-data-format
  137. ↑ KBpedia, 9 Gorffennaf 2020
  138. ↑ CAB Thesaurus, 6 Ebrill 2020
  139. ↑ ChEBI release 2020-09-01
  140. ↑ Cannabis Database
  141. ↑ ChEBI release 2019-10-02
  142. ↑ International Chemical Identifier, InChI=1S/C7H6O2/c8-7(9)6-4-2-1-3-5-6/h1-5H,(H,8,9)
  143. ↑ CosIng database, 28 Rhagfyr 2019, 32134, BENZOIC ACID, CAS no.: 65-85-0
  144. ↑ Immune Epitope Database and Analysis Resource, 1 Mawrth 2022, 139965
  145. ↑ Evaluations of the Joint FAO/WHO Expert Committee on Food Additives (JECFA), 13 Mai 2021
  146. ↑ EFSA database, 23 Ionawr 2021, CAS no.: 65-85-0, 08.021
  147. ↑ ChemSpider, 19 Tachwedd 2016, Saesneg, 238, Benzoic acid
  148. ↑ Hazardous Substances Data Bank, 10 Mai 2021, 28 Hydref 2019, BENZOIC ACID, 704
  149. ↑ 149.0 149.1 Gene Ontology release 2019-11-16
  150. ↑ DrugBank, Saesneg, 17 Tachwedd 2015, Benzoic Acid, 03793
  151. ↑ REGULATION (EC) No 1333/2008
  152. ↑ 152.0 152.1 Mesh ID, 15 Mawrth 2018, D019817
  153. ↑ inferred from InChI
  154. ↑ Basic laboratory and industrial chemicals: A CRC quick reference handbook
  155. ↑ 155.0 155.1 155.2 155.3 CRC Handbook of Chemistry and Physics (97th edition), 12-215
  156. ↑ 156.0 156.1 156.2 156.3 CRC Handbook of Chemistry and Physics (97th edition), 3-40
  157. ↑ 157.0 157.1 RD-02-00820
  158. ↑ 158.0 158.1 158.2 CRC Handbook of Chemistry and Physics (97th edition), 5-141
  159. ↑ CRC Handbook of Chemistry and Physics (97th edition), 5-173
  160. ↑ CRC Handbook of Chemistry and Physics (97th edition), 5-89
  161. ↑ 161.0 161.1 CRC Handbook of Chemistry and Physics (97th edition), 16-18
  162. ↑ A new antibiotic K-82 A and minor components, produced by Streptomyces lavendulae, strain No. K-82.
  163. ↑ The Evaluation of Capillary Zone and Micellar Electrokinetic Capillary Chromatographic Techniques for the Simultaneous Determination of Flavonoids, Cinnamic and Phenolic acids in Blackcurrant (Ribes nigrum) Bud Extracts
  164. ↑ Source of Balsam Poplar Buds
  165. ↑ Phenolic acids of Ephedra equisetina
  166. ↑ 166.00 166.01 166.02 166.03 166.04 166.05 166.06 166.07 166.08 166.09 166.10 166.11 166.12 166.13 166.14 166.15 166.16 166.17 166.18 Aromatic and fatty acids of triterpene esters and rubber content of Hoya latices and their taxonomic significance
  167. ↑ Studies on the Constituents of Osmorhiza aristata (THUNB.) MAKINO et YABE
  168. ↑ 168.0 168.1 Glycosidically bound aroma compounds in the fruits of Prunus species: apricot (P. armeniaca, L.), peach (P. persica, L.), yellow plum (P. domestica, L. ssp. syriaca)
  169. ↑ 3-Hydroxy-5,6-epoxy-.beta.-ionol .beta.-D-glucopyranoside and 3-hydroxy-7,8-dihydro-.beta.-ionol .beta.-D-glucopyranoside: New C13 norisoprenoid glucoconjugates from sloe tree (Prunus spinosa L.) leaves
  170. ↑ Acetylenes and terpenoids of Bellis perennis
  171. ↑ 171.0 171.1 171.2 171.3 Chemotaxonomy of section Leuce poplars by GC-MS of bud exudate
  172. ↑ 172.0 172.1 Bud exudate composition of Populus tremuloides
  173. ↑ Phenolic compounds isolated from bitter lupine seeds and their inhibitory effects on germination and seedling growth of lettuce
  174. ↑ Volatile components of plumeria flowers. Part 2.1 Plumeria rubra L. cv. ‘Irma Bryan’
  175. ↑ Notes: Analysis of Phenolics of Bud Exudate of Populus laurifolia by GC-MS
  176. ↑ Analysis of phenolics of bud exudate of Populus angustifolia by GC-MS
  177. ↑ 177.0 177.1 Notes: Analysis of Phenolics of Bud Exudate of Populus violascens by GC-MS
  178. ↑ Volatile compounds ofPolygala senega L. var.latifolia Torrey et Gray roots
  179. ↑ Volatile flavor components of licorice
  180. ↑ New types of antimicrobial compounds produced by Lactobacillus plantarum
  181. ↑ 181.0 181.1 Comparative chemical composition of the resinous exudates from Senecio adenotrichius and S. viscosissimus
  182. ↑ Separation, characterization, and quantitation of benzoic and phenolic antioxidants in American cranberry fruit by GC-MS.
  183. ↑ Coumaroyl Iridoids and a Depside from Cranberry (Vaccinium macrocarpon)
  184. ↑ 184.0 184.1 Benzoylglucoses from two Vaccinium species
  185. ↑ Separation and determination of flavonoids and other phenolic compounds in cranberry juice by high-performance liquid chromatography
  186. ↑ Inhibition of uropathogenic Escherichia coli by cranberry juice: a new antiadherence assay
  187. ↑ Cranberry phytochemicals: Isolation, structure elucidation, and their antiproliferative and antioxidant activities
  188. ↑ Biosafety, antioxidant status, and metabolites in urine after consumption of dried cranberry juice in healthy women: a pilot double-blind placebo-controlled trial.
  189. ↑ Coumaroyl iridoids and a depside from cranberry (Vaccinium macrocarpon).
  190. ↑ Microbial Inhibitors of Cranberries
  191. ↑ Characterization of Cranberry Benzoates and Their Antimicrobial Properties
  192. ↑ Nitrogen Form and Solution pH Effect on Organic Acid Content of Cranberry Roots and Shoots
  193. ↑ Phenolic analysis of bud exudate of Populus lasiocarpa by GC/MS
  194. ↑ Essential oil of Scutellaria baicalensis G.
  195. ↑ Phenolic Composition of Bud Exudates of Populus deltoides
  196. ↑ Chromatographic and chemometric investigation of the chemical defence mechanism of poplar tree genotypes against a bark fungine parasite
  197. ↑ Analysis of phenolics of bud exudate of Populus euphratica by GC-MS
  198. ↑ Volatile flavor components of malabar-nightshade (Basella rubra L.)
  199. ↑ A Novel Caffeic Acid Derivative and Other Constituents of Populus Bud Excretion and Propolis (Bee-Glue)
  200. ↑ Distribution of phenolic compounds in the seagrass Posidonia oceanica
  201. ↑ Phytotoxic substances in root exudates of cucumber (Cucumis sativus L.).
  202. ↑ 202.0 202.1 Polyphenolic Pattern in Apple Tree Leaves in Relation to Scab Resistance. A Preliminary Study
  203. ↑ 203.0 203.1 A comparative study on commercial samples of the roots of Paeonia vitchii and P. lactiflora
  204. ↑ Isolation and quantitative analysis of phenolic antioxidants, free sugars, and polyols from mango (Mangifera indica L.) stem bark aqueous decoction used in Cuba as a nutritional supplement
  205. ↑ Glycosidically-bound aroma volatile compounds in the skin and pulp of ‘Kensington Pride’ mango fruit at different stages of maturity
  206. ↑ Food quality and nutraceutical value of nine cultivars of mango (Mangifera indica L.) fruits grown in Mediterranean subtropical environment
  207. ↑ The Aroma of Cranberries. II. Vaccinium macrocarpon Ait.
  208. ↑ The Aroma of Cranberries. I. Vaccinium vitis-idaea L..
  209. ↑ 209.0 209.1 209.2 209.3 Chemistry of toxic range plants. Water-soluble lignols of Ponderosa pine needles
  210. ↑ Studies on the constituents of the seeds of Cassia obtusifolia Linn. The structures of three new anthraquinones.
  211. ↑ Diterpenes from Hoffmannia strigillosa
  212. ↑ A new monoterpene glycoside of Paeonia lactiflora
  213. ↑ Sesquiterpene lactones and flavonoids from Centaurea aspera
  214. ↑ Flavones, sesquiterpene lactones and glycosides isolated from Centaurea aspera var. Stenophylla
  215. ↑ Bioactive butenolides from Melodorum fruticosum
  216. ↑ Glycinoeclepins, Natural Hatching Stimuli for the Soybean Cyst Nematode,Heterodera Glycines. I. Isolation
  217. ↑ 9,10,13-TRIHYDROXYOCTADECANOIC ACID, A NEW FATTY ACID IN THE ROOTS OF KIDNEY BEAN (PHASEOLUS VULGARISL., “BENI-KINTOKI”)
  218. ↑ Plantago Major
  219. ↑ Contents from Plantago major
  220. ↑ Chemical consitituents from root of Isatis indigotica
  221. ↑ Chemical constituents of Isatis indigotica
  222. ↑ Antitubercular constituents from the stem wood of Cinnamomum kotoense
  223. ↑ Isolation of salicin derivatives from Homalium cochinchinensis and their antiviral activities
  224. ↑ Isolation of Salicin Derivatives from Homalium cochinchinensis and Their Antiviral Activities1
  225. ↑ Clerodane derivatives fromDiplostephium
  226. ↑ Oxytropis alkaloids II. Structure of oxytriphine
  227. ↑ Acidic metabolites from Phycomyces blakesleeanus
  228. ↑ Novel cytotoxic ring-a seco-cycloartane triterpenes from Gardenia coronaria and G. sootepensis
  229. ↑ Roripanoside, a New Kaempferol Rhamnoside fromRorippa Indica (L.) Hiern
  230. ↑ A sesquiterpene from Gardenia sootepensis
  231. ↑ 231.0 231.1 A novel retrodihydrochalcone from the stem bark of Uvaria mocoli
  232. ↑ 232.0 232.1 The Constituents of the Leaves of Aristolochia heterophylla HEMSL.
  233. ↑ The Constituents of the Stem and Roots of Aristolochia foveolata
  234. ↑ New monoterpene glycoside esters and phenolic constituents of Paeoniae radix, and increase of water solubility of proanthocyanidins in the presence of paeoniflorin
  235. ↑ Constituents of the pollen of Crocus sativus L. and their tyrosinase inhibitory activity
  236. ↑ Constituents of the Pollen of Crocus sativus L. and Their Tyrosinase Inhibitory Activity.
  237. ↑ Bioactive Butyrolactones from Fungi
  238. ↑ Bioactive Butyrolactones from Fungi.
  239. ↑ 239.0 239.1 Chemical Constituents of Taraxacum formosanum.
  240. ↑ 240.0 240.1 Chemical constituents of Taraxacum formosanum
  241. ↑ Cholinesterase Inhibitory Constituents from Onosma hispida.
  242. ↑ Cholinesterase inhibitory constituents from Onosma hispida
  243. ↑ Emodinol, beta-glucuronidase inhibiting triterpene from Paeonia emodi
  244. ↑ The Constituents and Synthesis of Cryptamygin-A from the Stem Bark ofCryptocarya Amygadalina
  245. ↑ Anti-platelet aggregation and chemical constituents from the rhizome of Gynura japonica.
  246. ↑ Cytotoxic and anti-HIV Principles from the Rhizomes of Begonia nantoensis.
  247. ↑ Cytotoxic and anti-HIV principles from the rhizomes of Begonia nantoensis
  248. ↑ Constituents from the Stems of Hibiscus taiwanensis.
  249. ↑ Constituents from the stems of Hibiscus taiwanensis.
  250. ↑ Volatile Compounds Secreted by the Oyster Mushroom (Pleurotus ostreatus)and Their Antibacterial Activities
  251. ↑ (−)-Loliolide and Other Germination Inhibitory Active Constituents inEquisetum Arvense
  252. ↑ 252.0 252.1 Chemical Constituents of a Heat-dried Chinese Mushroom,Hohenbuehelia serotina
  253. ↑ [Studies on the non-alkaloidal constituents of Aconitum japonicum thunb]
  254. ↑ Chemical constituents from roots of Ixeris chinensis
  255. ↑ Chemical constituents from the stems of Securidaca inappendiculata Hassk
  256. ↑ Sesquiterpenoids and (Z)-3-Hexenyl Glucoside from Pertya glabrescens and a Glucosidic Sesquiterpene from P. scandens
  257. ↑ Diterpenes derived from clerodanes from Pulicaria angustifolia
  258. ↑ Isolation, identification, and bioassay of toxic compounds from pine tree naturally infected by pine wood nematode.
  259. ↑ Two new acidic constituents of flue-cured Virginia tobacco
  260. ↑ Labdane acids and other components of the needles ofPinus pumila
  261. ↑ Alkaloids and phenolics of Wurmbea and Burchardia species
  262. ↑ 262.0 262.1 262.2 262.3 Alkaloids and phenolics of three Merendera species
  263. ↑ Sesquiterpene lactones, flavonoids and coumarins from Centaurea collina
  264. ↑ Chemical constituents of Eria spicata
  265. ↑ The hepatoprotective principle of Hypoestes triflora leaves
  266. ↑ Dramatic variation in diterpenoids of different populations of Bellardia trixago
  267. ↑ 5-methylcoumarins from Nassauvia species
  268. ↑ Organic acids from fresh California strawberries
  269. ↑ Analysis of the acid fraction of reunion geranium oil (Pelargonium graveolens L'Her. ex Ait)
  270. ↑ Benzoic acid biosynthesis in cell cultures of Hypericum androsaemum
  271. ↑ Stachylines A-D from the sponge-derived fungus Stachylidium sp.
  272. ↑ Ferruginenes A-C from Rhododendron ferrugineum and their cytotoxic evaluation
  273. ↑ Triterpenoid constituents from the roots of Paeonia rockii ssp. rockii.
  274. ↑ 274.0 274.1 Monoterpene glycosides from Paeonia hybrida
  275. ↑ 275.0 275.1 A monoterpene glucoside from Paeonia peregrina roots
  276. ↑ Two novel compounds from Paeonia suffructicosa
  277. ↑ Bioactive components, antioxidant and antimicrobial activities of Paeonia rockii fruit during development
  278. ↑ The response of Chlamydomonas reinhardtii to nitrogen deprivation: a systems biology analysis
  279. ↑ α-Pyrone Polyketides from Streptomyces ambofaciens BI0048, an Endophytic Actinobacterial Strain Isolated from the Red Alga Laurencia glandulifera.
  280. ↑ Defense responses in plants of Eucalyptus elicited by Streptomyces and challenged with Botrytis cinerea.
  281. ↑ Defensive and other secretions of the australian cocktail ant, iridomyrmex nitidiceps
  282. ↑ Biosynthesis of salicylic acid in fungus elicited Catharanthus roseus cells
  283. ↑ Flowering and Endogenous Levels of Benzoic Acid in Lemna Species
  284. ↑ 284.0 284.1 The Role of Plant Hormones and Benzoic Acid in Flowering of Lemna paucicostata 151 and 381
  285. ↑ Flavonoid metabolites in urine after oral administration of aqueous extract of Persea americana to rats
  286. ↑ Cysteine sulfoxide derivatives in Petiveria alliacea
  287. ↑ Isolation of 5-hydroxypyrrolidin-2-one and other constituents from the young fronds of Pteridium aquilinum
  288. ↑ Chemical and toxicological studies on bracken fern, Pteridium aquilinum var. latiusculum. I. Introduction, extraction and fractionation of constituents, and toxicological studies including carcinogenicity tests
  289. ↑ LXXIX.—The constituents of the flowers of Trifolium incarnatum
  290. ↑ Effect of phenolic compounds from Eucalyptus on the mycelial growth and conidial germination of Cryphonectria cubensis
  291. ↑ Some antifungal components of diseased Blue Ribbon iris bulbs
  292. ↑ Thin-layer high-vacuum distillation to isolate volatile flavour compounds of cocoa powder
  293. ↑ Phenolic compounds of Abies nephrolepis and their NO production inhibitory activities.
  294. ↑ Chemical Constituents of the Male Flower ofAlnus pendula(BETULACEAE)
  295. ↑ Chemical constituents of cape aloe and their synergistic growth-inhibiting effect on Ehrlich ascites tumor cells
  296. ↑ Polyphenols of the bark of Betula pendula
  297. ↑ Cytotoxic and anti-platelet aggregation constituents from the root wood of Melicope semecarpifolia
  298. ↑ Production of auxin and other indolic and phenolic compounds by Paenibacillus polymyxa strains isolated from different proximity to plant roots
  299. ↑ New benzoyl glucosides and cytotoxic pterosin sesquiterpenes from Pteris ensiformis Burm.
  300. ↑ New alkaloids from Tabernaemontana divaricata
  301. ↑ Recon 2.2: from reconstruction to model of human metabolism
  302. ↑ A community-driven global reconstruction of human metabolism.
  303. ↑ Metabolomic comparative analysis of the phloem sap of curry leaf tree (Bergera koenegii), orange jasmine (Murraya paniculata), and Valencia sweet orange (Citrus sinensis) supports their differential responses to Huanglongbing.
  304. ↑ Two new phenolic glycosides from the barks of Hydnocarpus annamensis and their anti-inflammatory and anti-oxidation activities
  305. ↑ CP VIOLATION IN Bs DECAYS
  306. ↑ Identification and Characterization of Phenylpropanoid Biosynthetic Genes and Their Accumulation in Bitter Melon (Momordica charantia).
  307. ↑ New Terpenoids from Chamaecyparis formosensis (Cupressaceae) Leaves with Modulatory Activity on Matrix Metalloproteases 2 and 9.
  308. ↑ 308.0 308.1 308.2 Populus candicans and the Balm of Gilead
  309. ↑ A chemical study of the roots of Paeonia anomala
  310. ↑ Chemistry and pharmacology of Rhaponticum carthamoides: a review.
  311. ↑ Flavonoids from the leaf resin of Adenostoma sparsifolium
  312. ↑ 312.0 312.1 Flavonoids and phenolic acids in adenostoma, a dominant genus of the californian chaparral
  313. ↑ Modeling Meets Metabolomics-The WormJam Consensus Model as Basis for Metabolic Studies in the Model Organism
  314. ↑ Bioassay-guided isolation of constituents of Piper sarmentosum using a mitochondrial transmembrane potential assay.
  315. ↑ Alkaloids from Tripterygium wilfordii Hook. Isolation and Structure of Wilforzine
  316. ↑ Free and glycosidically bound aroma compounds in cherry (Prunus avium L.).
  317. ↑ Metabolic profiles of sunflower genotypes with contrasting response to Sclerotinia sclerotiorum infection
  318. ↑ Volatile components of papaya (Carica papaya L., Solo variety)
  319. ↑ Differences in the metabolite profiles of spinach (Spinacia oleracea L.) leaf in different concentrations of nitrate in the culture solution
  320. ↑ THE INFLUENCE OF SEVERAL BENZENE DERIVATIVES ON THE ROOTS OF LUPINUS ALBUS
  321. ↑ Products of Dark CO(2) Fixation in Pea Root Nodules Support Bacteroid Metabolism
  322. ↑ Phenolic profiles, antihyperglycemic, antihyperlipidemic, and antioxidant properties of pomegranate (Punica granatum) peel extract
  323. ↑ Analysis of phenolic compounds in spruce needle extracts using an UV-VIS-diode array detector
  324. ↑ Metabolomic analysis of tomato seed germination
  325. ↑ Identification and characterization of metabolite quantitative trait loci in tomato leaves and comparison with those reported for fruits and seeds
  326. ↑ Cranberries and their bioactive constituents in human health
  327. ↑ Phytochemicals of cranberries and cranberry products: characterization, potential health effects, and processing stability
  328. ↑ Headspace Analysis of Osmanthus fragrans Lour.
  329. ↑ Volatile Flavor Components of Corn Tortillas and Related Products
  330. ↑ Wasabisides A-E, Lignan Glycosides from the Roots of Wasabia japonica.
  331. ↑ Constituents of the Leaves of Aristolochia kaempferi.
  332. ↑ "Essential oil constituents of \"PAEONIAE RADIX\" Peaonia lactiflora Pall. (P. albilora Pall.)."
  333. ↑ Volatile constituents of peony flowers
  334. ↑ Paeoniflorigenone, a new monoterpene from paeony roots
  335. ↑ The structure of paeoniflorigenone, a new monoterpene isolated from paenoiae radix.
  336. ↑ Capillary electrophoretic determination of the constituents of paeoniae radix
  337. ↑ Acaricidal activity of Paeonia suffruticosa root bark-derived compounds against Dermatophagoides farinae and Dermatophagoides pteronyssinus (Acari: Pyroglyphidae).
  338. ↑ Time-course metabolic profiling in alfalfa leaves under Phoma medicaginis infection
  339. ↑ Extracts from Pygeum africanum and other ethnobotanical species with antiandrogenic activity
  340. ↑ Activity-guided isolation of an antiandrogenic compound of Pygeum africanum
  341. ↑ Aromatic Substances in Leaves of Populus tremula as Inhibitors of Mycorrhizal Fungi
  342. ↑ Regulation of transcription of katE and katF in Escherichia coli
  343. ↑ Reactome, https://plantreactome.gramene.org/PathwayBrowser/#/R-OSA-2744345&DTAB=MT
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