17beta-Estradiol 3-(beta-D-glucuronide)

Details

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Internal ID 8bbc2e5f-825b-4483-9739-057a37574b92
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroidal glycosides > Steroid glucuronide conjugates
IUPAC Name (2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[[(8R,9S,13S,14S,17S)-17-hydroxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-yl]oxy]oxane-2-carboxylic acid
SMILES (Canonical) CC12CCC3C(C1CCC2O)CCC4=C3C=CC(=C4)OC5C(C(C(C(O5)C(=O)O)O)O)O
SMILES (Isomeric) C[C@]12CC[C@H]3[C@H]([C@@H]1CC[C@@H]2O)CCC4=C3C=CC(=C4)O[C@H]5[C@@H]([C@H]([C@@H]([C@H](O5)C(=O)O)O)O)O
InChI InChI=1S/C24H32O8/c1-24-9-8-14-13-5-3-12(10-11(13)2-4-15(14)16(24)6-7-17(24)25)31-23-20(28)18(26)19(27)21(32-23)22(29)30/h3,5,10,14-21,23,25-28H,2,4,6-9H2,1H3,(H,29,30)/t14-,15-,16+,17+,18+,19+,20-,21+,23-,24+/m1/s1
InChI Key MUOHJTRCBBDUOW-QXYWQCSFSA-N
Popularity 201 references in papers

Physical and Chemical Properties

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Molecular Formula C24H32O8
Molecular Weight 448.50 g/mol
Exact Mass 448.20971797 g/mol
Topological Polar Surface Area (TPSA) 137.00 Ų
XlogP 1.10
Atomic LogP (AlogP) 1.17
H-Bond Acceptor 7
H-Bond Donor 5
Rotatable Bonds 3

Synonyms

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Estradiol-3-glucuronide
17beta-Estradiol 3-(beta-D-glucuronide)
17beta-estradiol 3-glucuronide
Estradiol 3-Glucuronide
Estradiol-17beta 3-glucuronide
17beta-estradiol 3-glucosiduronic acid
CHEBI:36489
CHEMBL2074591
32835P5TLT
(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[[(8R,9S,13S,14S,17S)-17-hydroxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-yl]oxy]oxane-2-carboxylic acid
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 17beta-Estradiol 3-(beta-D-glucuronide)

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9050 90.50%
Caco-2 - 0.8600 86.00%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.7204 72.04%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9403 94.03%
OATP1B3 inhibitior + 0.9063 90.63%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9071 90.71%
BSEP inhibitior - 0.8983 89.83%
P-glycoprotein inhibitior - 0.7203 72.03%
P-glycoprotein substrate - 0.9151 91.51%
CYP3A4 substrate + 0.7618 76.18%
CYP2C9 substrate - 0.8103 81.03%
CYP2D6 substrate - 0.8642 86.42%
CYP3A4 inhibition - 0.8339 83.39%
CYP2C9 inhibition - 0.9271 92.71%
CYP2C19 inhibition - 0.7566 75.66%
CYP2D6 inhibition - 0.9229 92.29%
CYP1A2 inhibition - 0.5157 51.57%
CYP2C8 inhibition + 0.8996 89.96%
CYP inhibitory promiscuity - 0.9642 96.42%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5802 58.02%
Eye corrosion - 0.9927 99.27%
Eye irritation - 0.9494 94.94%
Skin irritation - 0.5705 57.05%
Skin corrosion - 0.9021 90.21%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6973 69.73%
Micronuclear - 0.8300 83.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation - 0.8696 86.96%
Respiratory toxicity + 0.9000 90.00%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity - 0.9373 93.73%
Acute Oral Toxicity (c) III 0.3488 34.88%
Estrogen receptor binding + 0.7441 74.41%
Androgen receptor binding + 0.7580 75.80%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.7277 72.77%
Aromatase binding + 0.6371 63.71%
PPAR gamma - 0.6701 67.01%
Honey bee toxicity - 0.8002 80.02%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity + 0.9772 97.72%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.31% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.06% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.08% 95.56%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 95.76% 89.05%
CHEMBL226 P30542 Adenosine A1 receptor 94.86% 95.93%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 94.42% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.96% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.83% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 91.76% 95.89%
CHEMBL2581 P07339 Cathepsin D 91.03% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 90.62% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.20% 97.09%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 88.20% 97.33%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 87.83% 90.71%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.68% 89.00%
CHEMBL2179 P04062 Beta-glucocerebrosidase 86.20% 85.31%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 85.54% 96.38%
CHEMBL4581 P52732 Kinesin-like protein 1 83.70% 93.18%
CHEMBL1951 P21397 Monoamine oxidase A 83.12% 91.49%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.84% 99.17%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 81.42% 96.09%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.36% 91.07%
CHEMBL3401 O75469 Pregnane X receptor 80.70% 94.73%
CHEMBL5028 O14672 ADAM10 80.21% 97.50%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 440713
LOTUS LTS0093510
wikiData Q27104364