(3R,5S,8R,9S,10S,13S,14S,16S,17S)-17-[(1S)-1-(dimethylamino)ethyl]-2',10,13-trimethylspiro[1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-3,3'-1H-isoindole]-16-ol

Details

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Internal ID 6ca41591-0d8a-4dc8-a1b7-39ce2e10ac99
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Hydroxysteroids > 16-hydroxysteroids
IUPAC Name (3R,5S,8R,9S,10S,13S,14S,16S,17S)-17-[(1S)-1-(dimethylamino)ethyl]-2',10,13-trimethylspiro[1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-3,3'-1H-isoindole]-16-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C31H48N2O/c1-20(32(4)5)28-27(34)17-26-23-12-11-22-18-31(24-10-8-7-9-21(24)19-33(31)6)16-15-29(22,2)25(23)13-14-30(26,28)3/h7-10,20,22-23,25-28,34H,11-19H2,1-6H3/t20-,22-,23+,25-,26-,27-,28-,29-,30-,31+/m0/s1
InChI Key QOPCQMMKSJQFBG-XYGVGCQLSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C31H48N2O
Molecular Weight 464.70 g/mol
Exact Mass 464.376664159 g/mol
Topological Polar Surface Area (TPSA) 26.70 Ų
XlogP 6.30
Atomic LogP (AlogP) 5.91
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3R,5S,8R,9S,10S,13S,14S,16S,17S)-17-[(1S)-1-(dimethylamino)ethyl]-2',10,13-trimethylspiro[1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-3,3'-1H-isoindole]-16-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9775 97.75%
Caco-2 - 0.5574 55.74%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.6221 62.21%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8694 86.94%
OATP1B3 inhibitior + 0.9410 94.10%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior + 0.6500 65.00%
BSEP inhibitior + 0.9745 97.45%
P-glycoprotein inhibitior + 0.6236 62.36%
P-glycoprotein substrate + 0.6502 65.02%
CYP3A4 substrate + 0.7656 76.56%
CYP2C9 substrate - 0.8204 82.04%
CYP2D6 substrate + 0.7157 71.57%
CYP3A4 inhibition - 0.7133 71.33%
CYP2C9 inhibition - 0.8190 81.90%
CYP2C19 inhibition - 0.7818 78.18%
CYP2D6 inhibition + 0.5575 55.75%
CYP1A2 inhibition - 0.8166 81.66%
CYP2C8 inhibition - 0.7108 71.08%
CYP inhibitory promiscuity - 0.9212 92.12%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.6553 65.53%
Eye corrosion - 0.9885 98.85%
Eye irritation - 0.9731 97.31%
Skin irritation - 0.7597 75.97%
Skin corrosion - 0.8423 84.23%
Ames mutagenesis - 0.7470 74.70%
Human Ether-a-go-go-Related Gene inhibition + 0.8120 81.20%
Micronuclear - 0.6400 64.00%
Hepatotoxicity - 0.5102 51.02%
skin sensitisation - 0.8445 84.45%
Respiratory toxicity + 0.9000 90.00%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity - 0.9383 93.83%
Acute Oral Toxicity (c) III 0.5298 52.98%
Estrogen receptor binding + 0.8547 85.47%
Androgen receptor binding + 0.7072 70.72%
Thyroid receptor binding + 0.6384 63.84%
Glucocorticoid receptor binding + 0.6489 64.89%
Aromatase binding + 0.7147 71.47%
PPAR gamma + 0.5352 53.52%
Honey bee toxicity - 0.7253 72.53%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.7867 78.67%

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 99.46% 96.09%
CHEMBL238 Q01959 Dopamine transporter 96.72% 95.88%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 96.03% 82.69%
CHEMBL2581 P07339 Cathepsin D 95.09% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 93.52% 90.17%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.78% 97.25%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 91.34% 94.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.97% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.89% 97.09%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 87.13% 95.89%
CHEMBL204 P00734 Thrombin 85.92% 96.01%
CHEMBL226 P30542 Adenosine A1 receptor 85.14% 95.93%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.89% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.88% 100.00%
CHEMBL4227 P25090 Lipoxin A4 receptor 83.44% 100.00%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 83.29% 100.00%
CHEMBL5028 O14672 ADAM10 82.73% 97.50%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.23% 97.14%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 80.76% 97.50%

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.
Pachysandra procumbens

Cross-Links

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PubChem 163105702
LOTUS LTS0165729
wikiData Q105225044