(3S,8R,9R,10S,13S,14R,17S)-10,13-dimethyl-17-[(1S)-1-[(2S)-5-methyl-3,4-dihydro-2H-pyrrol-2-yl]ethyl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol

Details

Top
Internal ID 099fd8c7-91be-4091-982a-e088d331e060
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Pregnane steroids > Gluco/mineralocorticoids, progestogins and derivatives
IUPAC Name (3S,8R,9R,10S,13S,14R,17S)-10,13-dimethyl-17-[(1S)-1-[(2S)-5-methyl-3,4-dihydro-2H-pyrrol-2-yl]ethyl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol
SMILES (Canonical) CC1=NC(CC1)C(C)C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)O)C)C
SMILES (Isomeric) CC1=N[C@@H](CC1)[C@@H](C)[C@@H]2CC[C@H]3[C@@]2(CC[C@@H]4[C@@H]3CC=C5[C@]4(CC[C@@H](C5)O)C)C
InChI InChI=1S/C26H41NO/c1-16-5-10-24(27-16)17(2)21-8-9-22-20-7-6-18-15-19(28)11-13-25(18,3)23(20)12-14-26(21,22)4/h6,17,19-24,28H,5,7-15H2,1-4H3/t17-,19-,20+,21-,22+,23+,24-,25+,26+/m0/s1
InChI Key HRXDXVGLJJYLNK-AYYDVIOASA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C26H41NO
Molecular Weight 383.60 g/mol
Exact Mass 383.318814931 g/mol
Topological Polar Surface Area (TPSA) 32.60 Ų
XlogP 5.40
Atomic LogP (AlogP) 6.19
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (3S,8R,9R,10S,13S,14R,17S)-10,13-dimethyl-17-[(1S)-1-[(2S)-5-methyl-3,4-dihydro-2H-pyrrol-2-yl]ethyl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.6926 69.26%
Blood Brain Barrier + 0.6879 68.79%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.4066 40.66%
OATP2B1 inhibitior - 0.7282 72.82%
OATP1B1 inhibitior + 0.9356 93.56%
OATP1B3 inhibitior + 0.9534 95.34%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior + 0.5500 55.00%
BSEP inhibitior + 0.8921 89.21%
P-glycoprotein inhibitior - 0.5550 55.50%
P-glycoprotein substrate + 0.6783 67.83%
CYP3A4 substrate + 0.7306 73.06%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7673 76.73%
CYP3A4 inhibition - 0.6305 63.05%
CYP2C9 inhibition - 0.8195 81.95%
CYP2C19 inhibition - 0.7627 76.27%
CYP2D6 inhibition - 0.8182 81.82%
CYP1A2 inhibition - 0.7719 77.19%
CYP2C8 inhibition + 0.5630 56.30%
CYP inhibitory promiscuity - 0.6171 61.71%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5152 51.52%
Eye corrosion - 0.9840 98.40%
Eye irritation - 0.9642 96.42%
Skin irritation - 0.6007 60.07%
Skin corrosion - 0.8675 86.75%
Ames mutagenesis - 0.7744 77.44%
Human Ether-a-go-go-Related Gene inhibition + 0.6831 68.31%
Micronuclear - 0.7700 77.00%
Hepatotoxicity + 0.6577 65.77%
skin sensitisation - 0.6879 68.79%
Respiratory toxicity + 0.8444 84.44%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity - 0.8814 88.14%
Acute Oral Toxicity (c) III 0.5906 59.06%
Estrogen receptor binding + 0.8530 85.30%
Androgen receptor binding + 0.8190 81.90%
Thyroid receptor binding + 0.6713 67.13%
Glucocorticoid receptor binding + 0.8088 80.88%
Aromatase binding - 0.5164 51.64%
PPAR gamma + 0.5191 51.91%
Honey bee toxicity - 0.7609 76.09%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.8700 87.00%

Targets

Top

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 95.78% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 92.98% 100.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 92.93% 95.89%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.00% 94.45%
CHEMBL2581 P07339 Cathepsin D 87.81% 98.95%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 86.21% 90.71%
CHEMBL221 P23219 Cyclooxygenase-1 85.05% 90.17%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 84.99% 89.05%
CHEMBL226 P30542 Adenosine A1 receptor 84.54% 95.93%
CHEMBL3359 P21462 Formyl peptide receptor 1 84.36% 93.56%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.30% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.12% 91.11%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 83.71% 93.40%
CHEMBL1871 P10275 Androgen Receptor 83.34% 96.43%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.20% 95.89%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.98% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.02% 97.09%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 80.05% 94.08%

Plants that contains it

Top
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.
Veratrum album

Cross-Links

Top
PubChem 162892386
LOTUS LTS0092571
wikiData Q105032877