(1S,2R,6S,7R,9R,11S,12S,15R,16S)-15-[(1S)-1-[(2R,4S,5R)-4,5-dimethyl-6-oxooxan-2-yl]-1-hydroxyethyl]-6,15-dihydroxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-4-en-3-one

Details

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Internal ID 3c844520-ce93-4199-880d-b1905f03446e
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroid lactones > Withanolides and derivatives
IUPAC Name (1S,2R,6S,7R,9R,11S,12S,15R,16S)-15-[(1S)-1-[(2R,4S,5R)-4,5-dimethyl-6-oxooxan-2-yl]-1-hydroxyethyl]-6,15-dihydroxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-4-en-3-one
SMILES (Canonical) CC1CC(OC(=O)C1C)C(C)(C2(CCC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6O)C)O5)C)O)O
SMILES (Isomeric) C[C@H]1C[C@@H](OC(=O)[C@@H]1C)[C@@](C)([C@]2(CC[C@@H]3[C@@]2(CC[C@H]4[C@H]3C[C@@H]5[C@]6([C@@]4(C(=O)C=C[C@@H]6O)C)O5)C)O)O
InChI InChI=1S/C28H40O7/c1-14-12-21(34-23(31)15(14)2)26(5,32)27(33)11-9-17-16-13-22-28(35-22)20(30)7-6-19(29)25(28,4)18(16)8-10-24(17,27)3/h6-7,14-18,20-22,30,32-33H,8-13H2,1-5H3/t14-,15+,16-,17-,18-,20-,21+,22+,24-,25-,26-,27+,28+/m0/s1
InChI Key ODFGLJQOCBLUPX-RQKGQDEBSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C28H40O7
Molecular Weight 488.60 g/mol
Exact Mass 488.27740361 g/mol
Topological Polar Surface Area (TPSA) 117.00 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.55
H-Bond Acceptor 7
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 (1S,2R,6S,7R,9R,11S,12S,15R,16S)-15-[(1S)-1-[(2R,4S,5R)-4,5-dimethyl-6-oxooxan-2-yl]-1-hydroxyethyl]-6,15-dihydroxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-4-en-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 + 0.8746 87.46%
Caco-2 - 0.7083 70.83%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.6855 68.55%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8521 85.21%
OATP1B3 inhibitior + 0.8455 84.55%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7321 73.21%
BSEP inhibitior - 0.4538 45.38%
P-glycoprotein inhibitior - 0.5180 51.80%
P-glycoprotein substrate + 0.5096 50.96%
CYP3A4 substrate + 0.7205 72.05%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8952 89.52%
CYP3A4 inhibition - 0.7243 72.43%
CYP2C9 inhibition - 0.8828 88.28%
CYP2C19 inhibition - 0.8569 85.69%
CYP2D6 inhibition - 0.9612 96.12%
CYP1A2 inhibition - 0.7485 74.85%
CYP2C8 inhibition + 0.5279 52.79%
CYP inhibitory promiscuity - 0.9919 99.19%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5890 58.90%
Eye corrosion - 0.9907 99.07%
Eye irritation - 0.9539 95.39%
Skin irritation + 0.5099 50.99%
Skin corrosion - 0.8886 88.86%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6583 65.83%
Micronuclear - 0.7200 72.00%
Hepatotoxicity + 0.7029 70.29%
skin sensitisation - 0.8554 85.54%
Respiratory toxicity + 0.8667 86.67%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity + 0.5192 51.92%
Acute Oral Toxicity (c) I 0.3945 39.45%
Estrogen receptor binding + 0.8184 81.84%
Androgen receptor binding + 0.7990 79.90%
Thyroid receptor binding + 0.6241 62.41%
Glucocorticoid receptor binding + 0.7339 73.39%
Aromatase binding + 0.7508 75.08%
PPAR gamma + 0.6075 60.75%
Honey bee toxicity - 0.7681 76.81%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.9727 97.27%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 98.29% 97.25%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.38% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.95% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.40% 95.56%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 90.53% 97.14%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.13% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.38% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.60% 96.09%
CHEMBL1871 P10275 Androgen Receptor 86.42% 96.43%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 86.00% 93.04%
CHEMBL2581 P07339 Cathepsin D 85.23% 98.95%
CHEMBL332 P03956 Matrix metalloproteinase-1 84.36% 94.50%
CHEMBL218 P21554 Cannabinoid CB1 receptor 83.75% 96.61%
CHEMBL3922 P50579 Methionine aminopeptidase 2 83.28% 97.28%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 82.45% 100.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 82.02% 82.69%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.12% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.59% 99.23%

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.
Deprea subtriflora
Physalis philadelphica

Cross-Links

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PubChem 12070588
LOTUS LTS0029222
wikiData Q105189813