[(1S)-1-[(3R,8S,9R,10R,12R,13S,14R,17S)-12-acetyloxy-3,8,14,17-tetrahydroxy-10-methyl-2,3,4,7,9,11,12,13,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl]ethyl] pyridine-2-carboxylate

Details

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Internal ID 11c41ad2-85d5-470a-b0ff-06223e2f6f16
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroid esters
IUPAC Name [(1S)-1-[(3R,8S,9R,10R,12R,13S,14R,17S)-12-acetyloxy-3,8,14,17-tetrahydroxy-10-methyl-2,3,4,7,9,11,12,13,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl]ethyl] pyridine-2-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C28H37NO8/c1-16(36-24(32)20-6-4-5-13-29-20)26(33)11-12-28(35)23(26)21(37-17(2)30)15-22-25(3)9-8-19(31)14-18(25)7-10-27(22,28)34/h4-7,13,16,19,21-23,31,33-35H,8-12,14-15H2,1-3H3/t16-,19+,21+,22+,23-,25-,26+,27-,28+/m0/s1
InChI Key IMMUOVQSDSHLHH-FXSBPKGLSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C28H37NO8
Molecular Weight 515.60 g/mol
Exact Mass 515.25191714 g/mol
Topological Polar Surface Area (TPSA) 146.00 Ų
XlogP 1.30
Atomic LogP (AlogP) 2.06
H-Bond Acceptor 9
H-Bond Donor 4
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(1S)-1-[(3R,8S,9R,10R,12R,13S,14R,17S)-12-acetyloxy-3,8,14,17-tetrahydroxy-10-methyl-2,3,4,7,9,11,12,13,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl]ethyl] pyridine-2-carboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9356 93.56%
Caco-2 - 0.8161 81.61%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.5736 57.36%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8977 89.77%
OATP1B3 inhibitior + 0.9009 90.09%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8571 85.71%
BSEP inhibitior + 0.9535 95.35%
P-glycoprotein inhibitior - 0.4799 47.99%
P-glycoprotein substrate + 0.5990 59.90%
CYP3A4 substrate + 0.7146 71.46%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8730 87.30%
CYP3A4 inhibition - 0.8940 89.40%
CYP2C9 inhibition - 0.8707 87.07%
CYP2C19 inhibition - 0.8375 83.75%
CYP2D6 inhibition - 0.9121 91.21%
CYP1A2 inhibition - 0.6035 60.35%
CYP2C8 inhibition + 0.7923 79.23%
CYP inhibitory promiscuity - 0.8686 86.86%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6040 60.40%
Eye corrosion - 0.9904 99.04%
Eye irritation - 0.9476 94.76%
Skin irritation - 0.6072 60.72%
Skin corrosion - 0.9263 92.63%
Ames mutagenesis - 0.7170 71.70%
Human Ether-a-go-go-Related Gene inhibition - 0.4376 43.76%
Micronuclear - 0.5500 55.00%
Hepatotoxicity + 0.5844 58.44%
skin sensitisation - 0.8488 84.88%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.9778 97.78%
Mitochondrial toxicity + 0.9250 92.50%
Nephrotoxicity - 0.6649 66.49%
Acute Oral Toxicity (c) III 0.4134 41.34%
Estrogen receptor binding + 0.7376 73.76%
Androgen receptor binding + 0.6970 69.70%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.6641 66.41%
Aromatase binding + 0.6434 64.34%
PPAR gamma - 0.5119 51.19%
Honey bee toxicity - 0.7139 71.39%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5155 51.55%
Fish aquatic toxicity + 0.9569 95.69%

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 98.61% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 98.02% 90.17%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 97.00% 94.62%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.68% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.01% 98.95%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 95.90% 94.08%
CHEMBL226 P30542 Adenosine A1 receptor 94.52% 95.93%
CHEMBL2243 O00519 Anandamide amidohydrolase 86.44% 97.53%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 85.88% 100.00%
CHEMBL211 P08172 Muscarinic acetylcholine receptor M2 84.97% 94.97%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.31% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.87% 86.33%
CHEMBL284 P27487 Dipeptidyl peptidase IV 83.53% 95.69%
CHEMBL1907598 P05106 Integrin alpha-V/beta-3 83.52% 95.71%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 83.17% 96.67%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.80% 85.14%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.16% 93.56%
CHEMBL5028 O14672 ADAM10 81.98% 97.50%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 81.24% 94.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.05% 89.00%

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.
Marsdenia rostrata

Cross-Links

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PubChem 162933806
LOTUS LTS0254488
wikiData Q105115781