Cholestatriene

Details

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Internal ID 407a8c05-d936-4883-9bb3-37c7d5d1ab12
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Cholestane steroids
IUPAC Name (8R,9S,10S,13S,14S,17R)-10,13-dimethyl-17-(6-methylhepta-2,4,6-trien-2-yl)-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H42/c1-19(2)9-8-10-20(3)23-14-15-24-22-13-12-21-11-6-7-17-26(21,4)25(22)16-18-27(23,24)5/h8-10,21-25H,1,6-7,11-18H2,2-5H3/t21?,22-,23+,24-,25-,26-,27+/m0/s1
InChI Key BJBPZEABVXLYLJ-LZHGKROGSA-N
Popularity 17 references in papers

Physical and Chemical Properties

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Molecular Formula C27H42
Molecular Weight 366.60 g/mol
Exact Mass 366.328651340 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 10.50
Atomic LogP (AlogP) 8.11
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Cholestatriene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9934 99.34%
Caco-2 + 0.6677 66.77%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Lysosomes 0.7752 77.52%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7864 78.64%
OATP1B3 inhibitior + 0.8190 81.90%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior + 0.9250 92.50%
P-glycoprotein inhibitior + 0.6320 63.20%
P-glycoprotein substrate - 0.7663 76.63%
CYP3A4 substrate + 0.7200 72.00%
CYP2C9 substrate - 0.6219 62.19%
CYP2D6 substrate - 0.7767 77.67%
CYP3A4 inhibition - 0.7341 73.41%
CYP2C9 inhibition - 0.7742 77.42%
CYP2C19 inhibition - 0.6230 62.30%
CYP2D6 inhibition - 0.9386 93.86%
CYP1A2 inhibition - 0.7771 77.71%
CYP2C8 inhibition - 0.6898 68.98%
CYP inhibitory promiscuity + 0.5000 50.00%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8100 81.00%
Carcinogenicity (trinary) Non-required 0.4518 45.18%
Eye corrosion - 0.9598 95.98%
Eye irritation - 0.9806 98.06%
Skin irritation - 0.6322 63.22%
Skin corrosion - 0.9687 96.87%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8165 81.65%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.6579 65.79%
skin sensitisation + 0.8079 80.79%
Respiratory toxicity + 0.8000 80.00%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity - 0.7917 79.17%
Acute Oral Toxicity (c) III 0.7598 75.98%
Estrogen receptor binding + 0.8930 89.30%
Androgen receptor binding + 0.7274 72.74%
Thyroid receptor binding + 0.6737 67.37%
Glucocorticoid receptor binding + 0.6981 69.81%
Aromatase binding + 0.6754 67.54%
PPAR gamma + 0.6393 63.93%
Honey bee toxicity - 0.6934 69.34%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL233 P35372 Mu opioid receptor 96.51% 97.93%
CHEMBL237 P41145 Kappa opioid receptor 94.19% 98.10%
CHEMBL1994 P08235 Mineralocorticoid receptor 92.23% 100.00%
CHEMBL4040 P28482 MAP kinase ERK2 91.33% 83.82%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 91.16% 91.79%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.00% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.09% 96.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 89.52% 92.94%
CHEMBL4370 P16662 UDP-glucuronosyltransferase 2B7 89.38% 100.00%
CHEMBL2061 P19793 Retinoid X receptor alpha 88.64% 91.67%
CHEMBL240 Q12809 HERG 87.69% 89.76%
CHEMBL1902 P62942 FK506-binding protein 1A 87.16% 97.05%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 86.23% 93.04%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 86.09% 85.30%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.88% 94.45%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 85.46% 96.38%
CHEMBL1907601 P11802 Cyclin-dependent kinase 4/cyclin D1 84.75% 98.99%
CHEMBL206 P03372 Estrogen receptor alpha 84.35% 97.64%
CHEMBL1871 P10275 Androgen Receptor 84.26% 96.43%
CHEMBL1937 Q92769 Histone deacetylase 2 84.21% 94.75%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 83.79% 95.50%
CHEMBL4482 O96013 Serine/threonine-protein kinase PAK 4 83.40% 95.42%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.09% 97.25%
CHEMBL3012 Q13946 Phosphodiesterase 7A 83.05% 99.29%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 82.54% 82.69%
CHEMBL259 P32245 Melanocortin receptor 4 81.87% 95.38%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 81.36% 80.96%
CHEMBL2004 P48443 Retinoid X receptor gamma 81.35% 100.00%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 81.21% 97.50%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 80.89% 95.58%
CHEMBL1870 P28702 Retinoid X receptor beta 80.80% 95.00%
CHEMBL5203 P33316 dUTP pyrophosphatase 80.28% 99.18%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 129634134
LOTUS LTS0140207
wikiData Q104376045