Epihippuristanol 11-One

Details

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Internal ID 7c92a184-89b5-48b6-ada2-0afdbc75c94a
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Furospirostanes and derivatives
IUPAC Name (1S,2S,3'S,4S,6S,7R,8R,9S,12S,13S,16R,18S)-7,16-dihydroxy-2',2',3',7,9,13-hexamethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,5'-oxolane]-11-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C28H44O5/c1-15-13-28(33-24(15,2)3)27(6,31)23-21(32-28)12-19-18-8-7-16-11-17(29)9-10-25(16,4)22(18)20(30)14-26(19,23)5/h15-19,21-23,29,31H,7-14H2,1-6H3/t15-,16-,17+,18-,19-,21-,22+,23-,25-,26-,27+,28-/m0/s1
InChI Key PYYCTSSONOEHSO-GORAVFDGSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C28H44O5
Molecular Weight 460.60 g/mol
Exact Mass 460.31887450 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 3.90
Atomic LogP (AlogP) 4.48
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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CHEMBL1221463
PYYCTSSONOEHSO-GORAVFDGSA-N
BDBM50482555

2D Structure

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2D Structure of Epihippuristanol 11-One

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9761 97.61%
Caco-2 - 0.5352 53.52%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.7607 76.07%
OATP2B1 inhibitior - 0.7194 71.94%
OATP1B1 inhibitior + 0.8903 89.03%
OATP1B3 inhibitior + 0.8295 82.95%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6571 65.71%
BSEP inhibitior - 0.5964 59.64%
P-glycoprotein inhibitior - 0.5854 58.54%
P-glycoprotein substrate + 0.5668 56.68%
CYP3A4 substrate + 0.7323 73.23%
CYP2C9 substrate - 0.6312 63.12%
CYP2D6 substrate - 0.8237 82.37%
CYP3A4 inhibition - 0.7933 79.33%
CYP2C9 inhibition - 0.9004 90.04%
CYP2C19 inhibition - 0.8746 87.46%
CYP2D6 inhibition - 0.9695 96.95%
CYP1A2 inhibition - 0.8020 80.20%
CYP2C8 inhibition - 0.5968 59.68%
CYP inhibitory promiscuity - 0.9706 97.06%
UGT catelyzed + 0.7362 73.62%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5022 50.22%
Eye corrosion - 0.9923 99.23%
Eye irritation - 0.9359 93.59%
Skin irritation + 0.5596 55.96%
Skin corrosion - 0.8752 87.52%
Ames mutagenesis - 0.6926 69.26%
Human Ether-a-go-go-Related Gene inhibition + 0.6421 64.21%
Micronuclear - 0.8900 89.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation - 0.8512 85.12%
Respiratory toxicity + 0.9000 90.00%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.8750 87.50%
Nephrotoxicity - 0.6539 65.39%
Acute Oral Toxicity (c) I 0.4439 44.39%
Estrogen receptor binding + 0.8220 82.20%
Androgen receptor binding + 0.7692 76.92%
Thyroid receptor binding + 0.6441 64.41%
Glucocorticoid receptor binding + 0.8024 80.24%
Aromatase binding + 0.7292 72.92%
PPAR gamma - 0.5472 54.72%
Honey bee toxicity - 0.7116 71.16%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9630 96.30%

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
CHEMBL1994 P08235 Mineralocorticoid receptor 93.64% 100.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.59% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.25% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.05% 96.09%
CHEMBL1871 P10275 Androgen Receptor 88.92% 96.43%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.24% 97.25%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 86.50% 93.04%
CHEMBL1902 P62942 FK506-binding protein 1A 86.49% 97.05%
CHEMBL299 P17252 Protein kinase C alpha 86.10% 98.03%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.74% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.09% 95.56%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 84.76% 96.77%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.97% 99.23%
CHEMBL3572 P11597 Cholesteryl ester transfer protein 80.99% 92.67%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.91% 95.89%
CHEMBL218 P21554 Cannabinoid CB1 receptor 80.34% 96.61%
CHEMBL2140 P48775 Tryptophan 2,3-dioxygenase 80.27% 98.46%

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 11453970
LOTUS LTS0261042
wikiData Q105216864