Methyl 5-(10,13-dimethyl-3-oxo-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl)-2-methylhex-3-enoate

Details

Top
Internal ID 52bb13aa-4817-4424-b914-f21ca0cebe49
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Pregnane steroids > Gluco/mineralocorticoids, progestogins and derivatives
IUPAC Name methyl 5-(10,13-dimethyl-3-oxo-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl)-2-methylhex-3-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H38O3/c1-17(6-7-18(2)25(29)30-5)22-10-11-23-21-9-8-19-16-20(28)12-14-26(19,3)24(21)13-15-27(22,23)4/h6-7,12,14,16-18,21-24H,8-11,13,15H2,1-5H3
InChI Key SPYDBHQUKUZVQJ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C27H38O3
Molecular Weight 410.60 g/mol
Exact Mass 410.28209507 g/mol
Topological Polar Surface Area (TPSA) 43.40 Ų
XlogP 6.60
Atomic LogP (AlogP) 5.91
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Methyl 5-(10,13-dimethyl-3-oxo-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl)-2-methylhex-3-enoate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9973 99.73%
Caco-2 + 0.4944 49.44%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.7930 79.30%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8494 84.94%
OATP1B3 inhibitior + 0.9700 97.00%
MATE1 inhibitior - 0.6400 64.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior + 0.9547 95.47%
P-glycoprotein inhibitior + 0.8231 82.31%
P-glycoprotein substrate - 0.7163 71.63%
CYP3A4 substrate + 0.7784 77.84%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9127 91.27%
CYP3A4 inhibition - 0.8746 87.46%
CYP2C9 inhibition - 0.7038 70.38%
CYP2C19 inhibition - 0.6361 63.61%
CYP2D6 inhibition - 0.9527 95.27%
CYP1A2 inhibition - 0.7663 76.63%
CYP2C8 inhibition + 0.4774 47.74%
CYP inhibitory promiscuity - 0.7935 79.35%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9620 96.20%
Carcinogenicity (trinary) Non-required 0.4968 49.68%
Eye corrosion - 0.9917 99.17%
Eye irritation - 0.9781 97.81%
Skin irritation - 0.5309 53.09%
Skin corrosion - 0.9733 97.33%
Ames mutagenesis - 0.7428 74.28%
Human Ether-a-go-go-Related Gene inhibition + 0.7810 78.10%
Micronuclear - 0.5900 59.00%
Hepatotoxicity - 0.5730 57.30%
skin sensitisation - 0.6568 65.68%
Respiratory toxicity + 0.9333 93.33%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.9250 92.50%
Nephrotoxicity - 0.9420 94.20%
Acute Oral Toxicity (c) III 0.7647 76.47%
Estrogen receptor binding + 0.8818 88.18%
Androgen receptor binding + 0.8723 87.23%
Thyroid receptor binding + 0.6586 65.86%
Glucocorticoid receptor binding + 0.7795 77.95%
Aromatase binding + 0.5973 59.73%
PPAR gamma - 0.5406 54.06%
Honey bee toxicity - 0.7802 78.02%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 1.0000 100.00%

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 97.54% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.01% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.48% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.77% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 91.57% 100.00%
CHEMBL226 P30542 Adenosine A1 receptor 91.17% 95.93%
CHEMBL221 P23219 Cyclooxygenase-1 91.15% 90.17%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.09% 97.25%
CHEMBL2581 P07339 Cathepsin D 91.00% 98.95%
CHEMBL1871 P10275 Androgen Receptor 89.84% 96.43%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 89.55% 96.38%
CHEMBL4072 P07858 Cathepsin B 87.82% 93.67%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 87.48% 90.71%
CHEMBL230 P35354 Cyclooxygenase-2 85.55% 89.63%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 85.40% 82.69%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 84.17% 91.07%
CHEMBL218 P21554 Cannabinoid CB1 receptor 83.50% 96.61%
CHEMBL3267 P48736 PI3-kinase p110-gamma subunit 83.30% 95.71%
CHEMBL340 P08684 Cytochrome P450 3A4 82.83% 91.19%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.75% 97.09%
CHEMBL5028 O14672 ADAM10 82.74% 97.50%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.74% 92.62%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.05% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.42% 89.00%

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.
There are no matching plants.

Cross-Links

Top
PubChem 72747988
LOTUS LTS0020209
wikiData Q105257683