(12beta,15beta,22R,23S,24S)-22,25-epoxy-12,15,23-trihydroxyergost-4,6,8(14)-trien-3-one

Details

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Internal ID 2b8cfa09-5fb4-478b-8d71-d9b74c91636b
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroidal glycosides
IUPAC Name (9R,10R,12R,13R,15R,17R)-12,15-dihydroxy-17-[(1S)-1-[(2R,3S,4S)-3-hydroxy-4,5,5-trimethyloxolan-2-yl]ethyl]-10,13-dimethyl-1,2,9,11,12,15,16,17-octahydrocyclopenta[a]phenanthren-3-one
SMILES (Canonical) CC1C(C(OC1(C)C)C(C)C2CC(C3=C4C=CC5=CC(=O)CCC5(C4CC(C23C)O)C)O)O
SMILES (Isomeric) C[C@H]1[C@@H]([C@H](OC1(C)C)[C@@H](C)[C@H]2C[C@H](C3=C4C=CC5=CC(=O)CC[C@@]5([C@H]4C[C@H]([C@]23C)O)C)O)O
InChI InChI=1S/C28H40O5/c1-14(25-24(32)15(2)26(3,4)33-25)19-12-21(30)23-18-8-7-16-11-17(29)9-10-27(16,5)20(18)13-22(31)28(19,23)6/h7-8,11,14-15,19-22,24-25,30-32H,9-10,12-13H2,1-6H3/t14-,15-,19+,20-,21+,22+,24-,25+,27-,28-/m0/s1
InChI Key FRSKOLKLHJBWOV-QCRCLYHDSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C28H40O5
Molecular Weight 456.60 g/mol
Exact Mass 456.28757437 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 2.20
Atomic LogP (AlogP) 3.73
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (12beta,15beta,22R,23S,24S)-22,25-epoxy-12,15,23-trihydroxyergost-4,6,8(14)-trien-3-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9939 99.39%
Caco-2 - 0.5810 58.10%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.7175 71.75%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8805 88.05%
OATP1B3 inhibitior + 0.9796 97.96%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior + 0.5936 59.36%
BSEP inhibitior + 0.7529 75.29%
P-glycoprotein inhibitior - 0.5298 52.98%
P-glycoprotein substrate + 0.5200 52.00%
CYP3A4 substrate + 0.6704 67.04%
CYP2C9 substrate - 0.8037 80.37%
CYP2D6 substrate - 0.8786 87.86%
CYP3A4 inhibition - 0.7660 76.60%
CYP2C9 inhibition - 0.8727 87.27%
CYP2C19 inhibition - 0.8588 85.88%
CYP2D6 inhibition - 0.9363 93.63%
CYP1A2 inhibition - 0.6242 62.42%
CYP2C8 inhibition - 0.5747 57.47%
CYP inhibitory promiscuity - 0.8394 83.94%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.4291 42.91%
Eye corrosion - 0.9921 99.21%
Eye irritation - 0.9586 95.86%
Skin irritation + 0.6595 65.95%
Skin corrosion - 0.9211 92.11%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5360 53.60%
Micronuclear - 0.9000 90.00%
Hepatotoxicity - 0.5394 53.94%
skin sensitisation - 0.7708 77.08%
Respiratory toxicity + 0.8111 81.11%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.9375 93.75%
Nephrotoxicity - 0.8749 87.49%
Acute Oral Toxicity (c) I 0.4622 46.22%
Estrogen receptor binding + 0.6917 69.17%
Androgen receptor binding + 0.7646 76.46%
Thyroid receptor binding + 0.6375 63.75%
Glucocorticoid receptor binding + 0.7245 72.45%
Aromatase binding + 0.5903 59.03%
PPAR gamma + 0.5436 54.36%
Honey bee toxicity - 0.7378 73.78%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9821 98.21%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.59% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.09% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 94.25% 91.49%
CHEMBL1994 P08235 Mineralocorticoid receptor 92.63% 100.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 91.87% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.66% 95.56%
CHEMBL221 P23219 Cyclooxygenase-1 89.06% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.86% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.08% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.42% 97.09%
CHEMBL2581 P07339 Cathepsin D 86.36% 98.95%
CHEMBL2039 P27338 Monoamine oxidase B 83.39% 92.51%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 82.83% 100.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.93% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.89% 86.33%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 81.75% 86.00%
CHEMBL4530 P00488 Coagulation factor XIII 80.83% 96.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.15% 99.23%

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 139585287
LOTUS LTS0006507
wikiData Q77387556