[(3S,8S,9R,10R,12R,13S,14R,17R)-17-acetyloxy-3,8,14,17-tetrahydroxy-10,13-dimethyl-1,2,3,4,7,9,11,12,15,16-decahydrocyclopenta[a]phenanthren-12-yl] (E)-3-phenylprop-2-enoate

Details

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Internal ID 386459a4-3ccf-4bd1-92e0-ccc6a64243b1
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroid esters
IUPAC Name [(3S,8S,9R,10R,12R,13S,14R,17R)-17-acetyloxy-3,8,14,17-tetrahydroxy-10,13-dimethyl-1,2,3,4,7,9,11,12,15,16-decahydrocyclopenta[a]phenanthren-12-yl] (E)-3-phenylprop-2-enoate
SMILES (Canonical) CC(=O)OC1(CCC2(C1(C(CC3C2(CC=C4C3(CCC(C4)O)C)O)OC(=O)C=CC5=CC=CC=C5)C)O)O
SMILES (Isomeric) CC(=O)O[C@@]1(CC[C@]2([C@@]1([C@@H](C[C@H]3[C@]2(CC=C4[C@@]3(CC[C@@H](C4)O)C)O)OC(=O)/C=C/C5=CC=CC=C5)C)O)O
InChI InChI=1S/C30H38O8/c1-19(31)38-30(36)16-15-29(35)27(30,3)24(37-25(33)10-9-20-7-5-4-6-8-20)18-23-26(2)13-12-22(32)17-21(26)11-14-28(23,29)34/h4-11,22-24,32,34-36H,12-18H2,1-3H3/b10-9+/t22-,23+,24+,26-,27-,28-,29+,30+/m0/s1
InChI Key FAKKXRBUOOLIHY-XMCCGYRLSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H38O8
Molecular Weight 526.60 g/mol
Exact Mass 526.25666817 g/mol
Topological Polar Surface Area (TPSA) 134.00 Ų
XlogP 3.10
Atomic LogP (AlogP) 3.03
H-Bond Acceptor 8
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 [(3S,8S,9R,10R,12R,13S,14R,17R)-17-acetyloxy-3,8,14,17-tetrahydroxy-10,13-dimethyl-1,2,3,4,7,9,11,12,15,16-decahydrocyclopenta[a]phenanthren-12-yl] (E)-3-phenylprop-2-enoate

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 - 0.7848 78.48%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.8067 80.67%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8616 86.16%
OATP1B3 inhibitior - 0.2370 23.70%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8374 83.74%
BSEP inhibitior + 0.9826 98.26%
P-glycoprotein inhibitior + 0.6602 66.02%
P-glycoprotein substrate + 0.5376 53.76%
CYP3A4 substrate + 0.7080 70.80%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8827 88.27%
CYP3A4 inhibition - 0.7957 79.57%
CYP2C9 inhibition - 0.7805 78.05%
CYP2C19 inhibition - 0.7712 77.12%
CYP2D6 inhibition - 0.9385 93.85%
CYP1A2 inhibition - 0.6635 66.35%
CYP2C8 inhibition + 0.8042 80.42%
CYP inhibitory promiscuity - 0.9435 94.35%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6260 62.60%
Eye corrosion - 0.9940 99.40%
Eye irritation - 0.9381 93.81%
Skin irritation + 0.6117 61.17%
Skin corrosion - 0.9371 93.71%
Ames mutagenesis - 0.7570 75.70%
Human Ether-a-go-go-Related Gene inhibition + 0.6953 69.53%
Micronuclear - 0.6800 68.00%
Hepatotoxicity - 0.5416 54.16%
skin sensitisation - 0.8551 85.51%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 1.0000 100.00%
Mitochondrial toxicity + 0.9750 97.50%
Nephrotoxicity - 0.7750 77.50%
Acute Oral Toxicity (c) IV 0.3692 36.92%
Estrogen receptor binding + 0.8327 83.27%
Androgen receptor binding + 0.7710 77.10%
Thyroid receptor binding + 0.5551 55.51%
Glucocorticoid receptor binding + 0.7707 77.07%
Aromatase binding + 0.7223 72.23%
PPAR gamma + 0.6314 63.14%
Honey bee toxicity - 0.7328 73.28%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.5445 54.45%
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
CHEMBL4040 P28482 MAP kinase ERK2 98.11% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.99% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.55% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.54% 86.33%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 96.21% 94.62%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 93.77% 96.00%
CHEMBL221 P23219 Cyclooxygenase-1 92.86% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.79% 95.56%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 91.29% 94.08%
CHEMBL2581 P07339 Cathepsin D 89.91% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.35% 89.00%
CHEMBL5028 O14672 ADAM10 89.23% 97.50%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 87.88% 95.50%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.60% 97.09%
CHEMBL5805 Q9NR97 Toll-like receptor 8 83.85% 96.25%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 82.98% 93.00%
CHEMBL4227 P25090 Lipoxin A4 receptor 81.43% 100.00%
CHEMBL226 P30542 Adenosine A1 receptor 80.67% 95.93%

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.
Araujia sericifera

Cross-Links

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PubChem 163068319
LOTUS LTS0008745
wikiData Q104992305