UCSF

ZINC18825330

Substance Information

In ZINC since Heavy atoms Benign functionality
October 14th, 2008 20 Yes

CAS Numbers: 446-72-0 , CAS# 446-72-0 , [446-72-0]

Other Names:

"Genistein, 99%"

1x7r

4 inverted exclamation marka,5,7-Trihydroxyisoflavone

4&prime

4',5, 7-Trihydroxyisoflavone

4',5, 7-Trihydroxyisoflavone;4',5,7-Trihydroxy-Isoflavone;4,5,7-Trihydroxy Iso-Flavone;5,7,4'-Trihydroxyisoflavone;5,7-Dihydroxy-3-(4-hydroxyphenyl)-4H-1-Benzopyran-4-one;Genistein;Genistein 85% HPLC;Genisteol;Genisterin;Prunetol;Sophoricol

4',5,7-Trihydroxy isoflavone

4',5,7-Trihydroxyisoflavone

4',5,7-Trihydroxyisoflavone; 4H-1-Benzopyran-4-one, 5,7-dihydroxy-3-(4-hydroxyphenyl)-; 5,7,4'-Trihydroxyisoflavone; 5,7-Dihydroxy-3-(4-hydroxyphenyl)-4-benzopyrone; BRN 0263823; C.I. 75610; C15H10O5; CCRIS 7675; Differenol A; EINECS 207-174-9; ENDOCRINE

4',5,7-trihydroxyisoflavone; 5,7-dihydroxy-3-(4-hydroxyphenyl)-4H-1-benzopyran-4-one; Differenol A

4,5,7-Trihydroxyiso-flavone

4,5,7-Trihydroxyisoflavone

4,6,7-Trihydroxyisoflavone

446-72-0

446-72-0; 5,7,4'-Trihydroxyisoflavone; C06563; Genistein

4?,5,7-Trihydroxyisoflavone

4H-1-Benzopyran-4-one, 5,7-dihydroxy-3-(4-hydroxyphenyl)-

5,7,4'-Trihydroxyisoflavone

5,7,4'-Trihydroxyisoflavone [446-72-0]; (Genistein, 98%)

5,7,4'-trihydroxyisoflavone; CPD-3141; genistein; isoflavone

5,7-Dihydroxy-3-(4-hydroxy-phenyl)-chromen-4-one

5,7-Dihydroxy-3-(4-hydroxyphenyl)-4-benzopyrone

5,7-Dihydroxy-3-(4-hydroxyphenyl)-4H-1-benzopyran-4-one

5,7-Dihydroxy-3-(4-hydroxyphenyl)-4H-chromen-4-one

5,7-dihydroxy-3-(4-hydroxyphenyl)chromen-4-one

5-18-04-00594 (Beilstein Handbook Reference)

800

AB1004490

AC-472

AC1NQXT4

ACon1_001065

AKOS001590147

BB_NC-1017

BIDD:ER0113

Bio1_000445

Bio1_000934

Bio1_001423

Bonistein

BRD-K43797669-001-02-3

BRD-K43797669-001-03-1

BRN 0263823

BSPBio_002375

C.I. 75610

C06563

CCRIS 7675

CHEBI:28088

CHEBI:42763; CHEBI:5302; CHEBI:24204

CHEMBL44

CID5280961

cMAP_000086

D019833

DB01645

DCL000330

Differenol A

DIHYDROXYHYDROXYPHENYLCHROMENON

DivK1c_006401

EINECS 207-174-9

ENDOCRINE DISRUPTOR (GENISTEIN) (SEE ALSO GENISTEIN (446-72-0))

EU-0100520

G 6649

G-2535

G0272

G10000

G6649_SIGMA

G6776_SIGMA

GEN

Genestein

GENISTEIN (ENDOCRINE DISRUPTER)

Genistein [446-72-0]; (5,7,4'-Trihydroxyisoflavone)

genistein(1-)

Genistein, 99%, synthetic

Genisteol

Genisterin

HSDB 7475

I06-0431

IN1327

ISOFLAVONE, 4',5,7-TRIHYDROXY-

K00046

KBio1_001345

KBio2_000800

KBio2_002564

KBio2_003368

KBio2_005132

KBio2_005936

KBio2_007700

KBio3_001595

KBio3_003042

KBioGR_002006

KBioGR_002564

KBioSS_000800

KBioSS_002573

Lactoferrin-genistein

LMPK12050218

LS-1266

MEGxp0_000568

MFCD00016952

MLS000738127

MolMap_000022

MolPort-000-003-911

N/A

NCGC00015479-01

NCGC00015479-02

NCGC00015479-05

NCGC00015479-13

NCGC00025005-01

NCGC00025005-02

NCGC00025005-03

NCGC00025005-04

NCGC00025005-05

NCGC00025005-06

NCGC00025005-07

NCGC00169711-01

NCGC00169711-02

nchembio.168-comp7

nchembio.2007.28-comp32

nchembio.76-comp6

NCI60_003369

NPI 031L

NSC 36586

NSC36586

Oprea1_224620

Oprea1_437815

OR-2321

Prunetol

Prunetol; GENISTEIN; Genistein; GENISTEIN; Genisteol; Sophoricol; C.I. 75610; Genisterin; 4',5,7-Trihydroxyisoflavone

Prunetol; Sophoricol

PTI G4660 (Genistein)

PTI-G4660

S1342_Selleck

SIPI 807-1

SIPI-9764-I

SMP1_000133

SMR000112580

Sophoricol

SPBio_000636

SpecPlus_000305

SPECTRUM210296

Spectrum2_000638

Spectrum3_000678

Spectrum4_001543

Spectrum5_000106

Spectrum_000320

STK801619

STO514

TNP00151

Tocris-1110

UPCMLD-DP096

UPCMLD-DP096:001

ZINC18825330

Download: MOL2 SDF SMILES Flexibase

Annotations

Vendors

Physical Representations

Type pH range xlogP Des A‑Pol Apolar desolvation (kcal/mol) Des Pol Polar desolvation (kcal/mol) H Don H-bond donors H Acc H-bond acceptors Chg Net charge tPSA (Ų) MWT Molecular weight (g/mol) RB Rotatable bonds DL
Ref Reference (pH 7) 2.27 1.08 -13.3 3 5 0 91 270.24 1

Vendor Notes

Note Type Comments Provided By
biological_source V. widely distributed in the Leguminosae subf. Papilionoideae but also in Podocarpus spicatus (Podocarpaceae) and Prunus spp. (Rosaceae). Also prod. by microorganisms Streptomyce ZereneX Building Blocks
Molecular_Solubility 2.344 Bitter DB
mechanism . ZereneX Building Blocks
ALOGPS_SOLUBILITY 1.23e-01 g/l DrugBank-experimental
Mp [°C] 297 - 298 Acros Organics
M.P 306C Indofine
UniProt Database Links 7OMT6_MEDSA; 7OMT8_MEDSA; 7OMT9_MEDSA; AOXA_RAT; DHRS4_BOVIN; DHRS4_HUMAN; DHRS4_MOUSE; DHRS4_PIG; DHRS4_PONAB; DHRS4_RABIT; DHRS4_RAT; GBA3_HUMAN; HGGL_SECCE; HIDH_SOYBN; HIDM_GLYEC; I4OMT_MEDTR; I7GT1_SOYBN; NOLA_BRADU; SHB_MOUSE; SOMT2_SOYBN; U73B2_ARA ChEBI
Purity 99% APIChem
Purity >98% Fluorochem
mechanism Against protein tyrosine kinases including those activated by epidermal growth factor (EGRF) and platelet derived growth factor (PDGF) receptors IBScreen Bioactives
biological_use Antioxidant IBScreen Bioactives
biological_use Claimed antineoplastic preventative activity IBScreen Bioactives
Therapy Cytotoxic inhibitor of tyrosine kinase and topoisomerase II kinase SMDC Iconix
Patent Database Links EP0827698; EP0829261; EP1038531; EP1046396; EP1166643; EP1174144; EP1232756; EP1566176; EP1634601; EP1634607; EP1656942; EP1669080; EP1767215; EP1779858; EP1806135; EP1808169; EP1808172; EP1834636; EP1842567; EP1854462; EP1878445; EP1897530; EP1897551; EP ChEBI
therap increases bone mineral density MicroSource Spectrum
Notes Inhibitor of tyrosine protein kinase Apollo Scientific Bioactives
Warnings IRRITANT Matrix Scientific
Indications natural flavonoid food suppliment KeyOrganics Bioactives
APPEARANCE Pale yellow powder Indofine
mechanism Protein kinase inhibitor IBScreen Bioactives IBScreen Bioactives
S phrase S24/25: Avoid contact with skin and eyes. Acros Organics
Target Serine/threonine-protein kinase PLK2(Q9NYY3)&G2/mitotic-specific cyclin-B1(P14635)&Telomerase protein component 1(Q99973)&Signal transducer and activator of transcription 3(P40763)&Estrogen receptor(P03372)&Estrogen receptor beta(Q92731)&Scaffold attachme Herbal Ingredients Targets
biological_use Shows insect antifeedant and weak antibacterial activity against E. coli and Xanthomonas oryzae IBScreen Bioactives
SOLUBILITY Soluble in DMSO Indofine
SOLUBILITY Soluble in DMSO and ethanol Indofine
Target Topoisomerase; EGFR Selleck Chemicals
biological_use Weak estrogen IBScreen Bioactives IBScreen Bioactives
APPEARANCE White powder Indofine
M.P. ~306-308 C (dec) Indofine
MP ~306-308o C Indofine

Activity (Go SEA)

Clustered Target Annotations
Code Description Organism Class Affinity (nM) LE (kcal/mol/atom) Type
AA1R-2-E Adenosine A1 Receptor (cluster #2 Of 4), Eukaryotic Eukaryotes 5000 0.37 Binding ≤ 10μM
ABCG2-1-E ATP-binding Cassette Sub-family G Member 2 (cluster #1 Of 2), Eukaryotic Eukaryotes 8800 0.35 Binding ≤ 10μM
ABL1-1-E Tyrosine-protein Kinase ABL (cluster #1 Of 1), Eukaryotic Eukaryotes 10000 0.35 Binding ≤ 10μM
AOFA-4-E Monoamine Oxidase A (cluster #4 Of 8), Eukaryotic Eukaryotes 900 0.42 Binding ≤ 10μM
AOFB-4-E Monoamine Oxidase B (cluster #4 Of 8), Eukaryotic Eukaryotes 900 0.42 Binding ≤ 10μM
DHB1-1-E Estradiol 17-beta-dehydrogenase 1 (cluster #1 Of 1), Eukaryotic Eukaryotes 2210 0.40 Binding ≤ 10μM
EGFR-2-E Epidermal Growth Factor Receptor ErbB1 (cluster #2 Of 4), Eukaryotic Eukaryotes 2600 0.39 Binding ≤ 10μM
ERR1-1-E Estrogen-related Receptor Alpha (cluster #1 Of 1), Eukaryotic Eukaryotes 10 0.56 Binding ≤ 10μM
ERR2-1-E Estrogen-related Receptor Beta (cluster #1 Of 1), Eukaryotic Eukaryotes 395 0.45 Binding ≤ 10μM
ESR1-1-E Estrogen Receptor Alpha (cluster #1 Of 5), Eukaryotic Eukaryotes 990 0.42 Binding ≤ 10μM
ESR2-4-E Estrogen Receptor Beta (cluster #4 Of 4), Eukaryotic Eukaryotes 990 0.42 Binding ≤ 10μM
MGA-3-E Maltase-glucoamylase (cluster #3 Of 3), Eukaryotic Eukaryotes 2610 0.39 Binding ≤ 10μM
Q965D7-2-E Fatty Acid Synthase (cluster #2 Of 2), Eukaryotic Eukaryotes 7000 0.36 Binding ≤ 10μM
ESR1-1-E Estrogen Receptor Alpha (cluster #1 Of 3), Eukaryotic Eukaryotes 950 0.42 Functional ≤ 10μM
ESR2-2-E Estrogen Receptor Beta (cluster #2 Of 2), Eukaryotic Eukaryotes 956 0.42 Functional ≤ 10μM
ADO-1-E Aldehyde Oxidase (cluster #1 Of 3), Eukaryotic Eukaryotes 340 0.45 ADME/T ≤ 10μM
Z50420-1-O Trypanosoma Brucei Brucei (cluster #1 Of 7), Other Other 4200 0.38 Functional ≤ 10μM
Z80030-1-O ANN-1 (cluster #1 Of 2), Other Other 8000 0.36 Functional ≤ 10μM
Z80037-1-O Balb/MK (cluster #1 Of 1), Other Other 9100 0.35 Functional ≤ 10μM
Z80224-1-O MCF7 (Breast Carcinoma Cells) (cluster #1 Of 14), Other Other 1000 0.42 Functional ≤ 10μM
Z81068-1-O Ishikawa (Uterine Carcinoma Cells) (cluster #1 Of 1), Other Other 510 0.44 Functional ≤ 10μM
Z81247-2-O HeLa (Cervical Adenocarcinoma Cells) (cluster #2 Of 9), Other Other 956 0.42 Functional ≤ 10μM
ChEMBL Target Annotations
Uniprot Swissprot Description Affinity (nM) LE (kcal/mol/atom) Type
EGFR_HUMAN P00533 Epidermal Growth Factor Receptor ErbB1, Human 1000 0.42 Binding ≤ 1μM
ESR1_HUMAN P03372 Estrogen Receptor Alpha, Human 20 0.54 Binding ≤ 1μM
ESR2_HUMAN Q92731 Estrogen Receptor Beta, Human 1.3 0.62 Binding ≤ 1μM
ERR1_HUMAN P11474 Estrogen-related Receptor Alpha, Human 10 0.56 Binding ≤ 1μM
ERR2_HUMAN O95718 Estrogen-related Receptor Beta, Human 395 0.45 Binding ≤ 1μM
AOFA_HUMAN P21397 Monoamine Oxidase A, Human 900 0.42 Binding ≤ 1μM
AOFB_HUMAN P27338 Monoamine Oxidase B, Human 900 0.42 Binding ≤ 1μM
AA1R_RAT P25099 Adenosine A1 Receptor, Rat 5000 0.37 Binding ≤ 10μM
ABCG2_HUMAN Q9UNQ0 ATP-binding Cassette Sub-family G Member 2, Human 6900 0.36 Binding ≤ 10μM
EGFR_HUMAN P00533 Epidermal Growth Factor Receptor ErbB1, Human 1000 0.42 Binding ≤ 10μM
DHB1_HUMAN P14061 Estradiol 17-beta-dehydrogenase 1, Human 2210 0.40 Binding ≤ 10μM
ESR1_HUMAN P03372 Estrogen Receptor Alpha, Human 1145 0.42 Binding ≤ 10μM
ESR2_HUMAN Q92731 Estrogen Receptor Beta, Human 1.3 0.62 Binding ≤ 10μM
ERR1_HUMAN P11474 Estrogen-related Receptor Alpha, Human 10 0.56 Binding ≤ 10μM
ERR2_HUMAN O95718 Estrogen-related Receptor Beta, Human 395 0.45 Binding ≤ 10μM
Q965D7_PLAFA Q965D7 Fatty Acid Synthase, Plafa 7000 0.36 Binding ≤ 10μM
MGA_HUMAN O43451 Maltase-glucoamylase, Human 2610 0.39 Binding ≤ 10μM
AOFA_HUMAN P21397 Monoamine Oxidase A, Human 900 0.42 Binding ≤ 10μM
AOFB_HUMAN P27338 Monoamine Oxidase B, Human 900 0.42 Binding ≤ 10μM
ABL1_HUMAN P00519 Tyrosine-protein Kinase ABL, Human 10000 0.35 Binding ≤ 10μM
Z80030 Z80030 ANN-1 8000 0.36 Functional ≤ 10μM
Z80037 Z80037 Balb/MK 9100 0.35 Functional ≤ 10μM
ESR1_HUMAN P03372 Estrogen Receptor Alpha, Human 810 0.43 Functional ≤ 10μM
ESR2_HUMAN Q92731 Estrogen Receptor Beta, Human 1.7 0.61 Functional ≤ 10μM
Z81247 Z81247 HeLa (Cervical Adenocarcinoma Cells) 73 0.50 Functional ≤ 10μM
Z81068 Z81068 Ishikawa (Uterine Carcinoma Cells) 510 0.44 Functional ≤ 10μM
Z80224 Z80224 MCF7 (Breast Carcinoma Cells) 1000 0.42 Functional ≤ 10μM
Z50420 Z50420 Trypanosoma Brucei Brucei 4200 0.38 Functional ≤ 10μM
ADO_HUMAN Q06278 Aldehyde Oxidase, Human 340 0.45 ADME/T ≤ 10μM

Reactome Annotations from Targets (via Uniprot)

Description Species
Abacavir transmembrane transport
Adenosine P1 receptors
CDO in myogenesis
Constitutive PI3K/AKT Signaling in Cancer
Digestion of dietary carbohydrate
EGFR downregulation
EGFR interacts with phospholipase C-gamma
EGFR Transactivation by Gastrin
Enzymatic degradation of dopamine by COMT
Enzymatic degradation of Dopamine by monoamine oxidase
Estrogen biosynthesis
Factors involved in megakaryocyte development and platelet production
G alpha (i) signalling events
GAB1 signalosome
GRB2 events in EGFR signaling
GRB2 events in ERBB2 signaling
Iron uptake and transport
Metabolism of serotonin
Monoamines are oxidized to aldehydes by MAOA and MAOB, producing NH3 and H2O2
Norepinephrine Neurotransmitter Release Cycle
Nuclear Receptor transcription pathway
Nuclear signaling by ERBB4
PI3K events in ERBB2 signaling
PIP3 activates AKT signaling
PLCG1 events in ERBB2 signaling
PPARA activates gene expression
Regulation of actin dynamics for phagocytic cup formation
Role of Abl in Robo-Slit signaling
SHC1 events in EGFR signaling
SHC1 events in ERBB2 signaling
Signal transduction by L1
Signaling by constitutively active EGFR
Signaling by EGFR
Signaling by ERBB2
Signaling by ERBB4
The canonical retinoid cycle in rods (twilight vision)
Transcriptional activation of mitochondrial biogenesis
Vitamins B6 activation to pyridoxal phosphate

Analogs ( Draw Identity 99% 90% 80% 70% )