[(3S,7S,8S,9S,10S,13R,14S,17R)-3,7-dihydroxy-13-methyl-17-[(2R)-6-methyl-5-methylideneheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-10-yl]methyl acetate

Details

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Internal ID 04930ef6-ad8c-46b2-b1c9-ae61d5400a92
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Ergostane steroids > Ergosterols and derivatives
IUPAC Name [(3S,7S,8S,9S,10S,13R,14S,17R)-3,7-dihydroxy-13-methyl-17-[(2R)-6-methyl-5-methylideneheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-10-yl]methyl acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H48O4/c1-18(2)19(3)7-8-20(4)24-9-10-25-28-26(12-13-29(24,25)6)30(17-34-21(5)31)14-11-23(32)15-22(30)16-27(28)33/h16,18,20,23-28,32-33H,3,7-15,17H2,1-2,4-6H3/t20-,23+,24-,25+,26+,27-,28+,29-,30-/m1/s1
InChI Key PZJQZZOSDDOIDL-HKEGKLTRSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C30H48O4
Molecular Weight 472.70 g/mol
Exact Mass 472.35526001 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 6.90
Atomic LogP (AlogP) 6.07
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(3S,7S,8S,9S,10S,13R,14S,17R)-3,7-dihydroxy-13-methyl-17-[(2R)-6-methyl-5-methylideneheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-10-yl]methyl acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9938 99.38%
Caco-2 - 0.6472 64.72%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.8781 87.81%
OATP2B1 inhibitior - 0.5731 57.31%
OATP1B1 inhibitior + 0.7929 79.29%
OATP1B3 inhibitior - 0.2376 23.76%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.5661 56.61%
BSEP inhibitior + 0.8708 87.08%
P-glycoprotein inhibitior - 0.4501 45.01%
P-glycoprotein substrate + 0.5511 55.11%
CYP3A4 substrate + 0.7410 74.10%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8465 84.65%
CYP3A4 inhibition - 0.8423 84.23%
CYP2C9 inhibition - 0.8196 81.96%
CYP2C19 inhibition - 0.9189 91.89%
CYP2D6 inhibition - 0.9387 93.87%
CYP1A2 inhibition - 0.8886 88.86%
CYP2C8 inhibition + 0.5581 55.81%
CYP inhibitory promiscuity - 0.7974 79.74%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6868 68.68%
Eye corrosion - 0.9933 99.33%
Eye irritation - 0.9522 95.22%
Skin irritation + 0.5833 58.33%
Skin corrosion - 0.9626 96.26%
Ames mutagenesis - 0.6283 62.83%
Human Ether-a-go-go-Related Gene inhibition + 0.6631 66.31%
Micronuclear - 0.8300 83.00%
Hepatotoxicity + 0.5264 52.64%
skin sensitisation - 0.8128 81.28%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity - 0.5561 55.61%
Acute Oral Toxicity (c) III 0.7179 71.79%
Estrogen receptor binding + 0.8371 83.71%
Androgen receptor binding + 0.7412 74.12%
Thyroid receptor binding - 0.4884 48.84%
Glucocorticoid receptor binding + 0.7423 74.23%
Aromatase binding + 0.6081 60.81%
PPAR gamma + 0.6092 60.92%
Honey bee toxicity - 0.6553 65.53%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6255 62.55%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.74% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.40% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.19% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.51% 94.45%
CHEMBL2581 P07339 Cathepsin D 91.45% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 89.80% 90.17%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.14% 100.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 89.05% 82.69%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 88.23% 95.89%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 88.12% 93.04%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.80% 97.09%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 87.41% 90.71%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.17% 95.89%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.29% 92.62%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.80% 86.33%
CHEMBL2782 P35610 Acyl coenzyme A:cholesterol acyltransferase 1 82.74% 91.65%
CHEMBL4227 P25090 Lipoxin A4 receptor 81.31% 100.00%
CHEMBL5028 O14672 ADAM10 81.11% 97.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.40% 99.17%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
There are no matching plants.

Cross-Links

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PubChem 16751607
LOTUS LTS0110603
wikiData Q105216998