1-[(3S,8R,9S,10R,13R,14S,17S)-14-hydroxy-10,13-dimethyl-3-[(2R,3S,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-1,2,3,4,7,8,9,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl]ethanone

Details

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Internal ID 99278446-d923-426d-8aa2-1a951a125d53
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroidal glycosides
IUPAC Name 1-[(3S,8R,9S,10R,13R,14S,17S)-14-hydroxy-10,13-dimethyl-3-[(2R,3S,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-1,2,3,4,7,8,9,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl]ethanone
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H42O7/c1-14(28)18-9-12-27(32)20-6-5-16-13-17(34-24-23(31)22(30)21(29)15(2)33-24)7-10-25(16,3)19(20)8-11-26(18,27)4/h5,15,17-24,29-32H,6-13H2,1-4H3/t15-,17-,18+,19-,20+,21+,22+,23-,24-,25-,26+,27-/m0/s1
InChI Key FQXKZRWLIJVZPF-YTRYOHOFSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C27H42O7
Molecular Weight 478.60 g/mol
Exact Mass 478.29305367 g/mol
Topological Polar Surface Area (TPSA) 116.00 Ų
XlogP 1.50
Atomic LogP (AlogP) 2.48
H-Bond Acceptor 7
H-Bond Donor 4
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-[(3S,8R,9S,10R,13R,14S,17S)-14-hydroxy-10,13-dimethyl-3-[(2R,3S,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-1,2,3,4,7,8,9,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl]ethanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9263 92.63%
Caco-2 - 0.7744 77.44%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.7295 72.95%
OATP2B1 inhibitior - 0.7165 71.65%
OATP1B1 inhibitior + 0.9018 90.18%
OATP1B3 inhibitior + 0.8725 87.25%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7071 70.71%
BSEP inhibitior - 0.5776 57.76%
P-glycoprotein inhibitior - 0.6177 61.77%
P-glycoprotein substrate - 0.6442 64.42%
CYP3A4 substrate + 0.7093 70.93%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8661 86.61%
CYP3A4 inhibition - 0.8627 86.27%
CYP2C9 inhibition - 0.9015 90.15%
CYP2C19 inhibition - 0.8833 88.33%
CYP2D6 inhibition - 0.9372 93.72%
CYP1A2 inhibition - 0.7860 78.60%
CYP2C8 inhibition + 0.6181 61.81%
CYP inhibitory promiscuity - 0.9482 94.82%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6211 62.11%
Eye corrosion - 0.9916 99.16%
Eye irritation - 0.9645 96.45%
Skin irritation + 0.6191 61.91%
Skin corrosion - 0.9244 92.44%
Ames mutagenesis - 0.8154 81.54%
Human Ether-a-go-go-Related Gene inhibition - 0.4138 41.38%
Micronuclear - 0.7900 79.00%
Hepatotoxicity - 0.7551 75.51%
skin sensitisation - 0.8542 85.42%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.9444 94.44%
Mitochondrial toxicity + 0.8625 86.25%
Nephrotoxicity - 0.5990 59.90%
Acute Oral Toxicity (c) I 0.3206 32.06%
Estrogen receptor binding + 0.6923 69.23%
Androgen receptor binding + 0.6790 67.90%
Thyroid receptor binding - 0.5294 52.94%
Glucocorticoid receptor binding + 0.7350 73.50%
Aromatase binding + 0.6098 60.98%
PPAR gamma - 0.6137 61.37%
Honey bee toxicity - 0.7910 79.10%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5095 50.95%
Fish aquatic toxicity + 0.9751 97.51%

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 97.96% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.33% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.42% 97.25%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.76% 89.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 91.94% 100.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.37% 86.33%
CHEMBL2581 P07339 Cathepsin D 87.43% 98.95%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.73% 95.89%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 86.50% 89.05%
CHEMBL241 Q14432 Phosphodiesterase 3A 86.33% 92.94%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 84.79% 95.89%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.57% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.55% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.99% 95.56%
CHEMBL5028 O14672 ADAM10 80.79% 97.50%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.73% 93.04%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.47% 91.07%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.37% 97.09%
CHEMBL5255 O00206 Toll-like receptor 4 80.22% 92.50%

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.
Marsdenia roylei

Cross-Links

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PubChem 11282994
LOTUS LTS0210579
wikiData Q104999984