Lophenol

Details

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Internal ID ffd0c093-4088-499c-81c5-dd95ae83796c
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Cholestane steroids > Cholesterols and derivatives
IUPAC Name (3S,4S,5S,9R,10S,13R,14R,17R)-4,10,13-trimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol
SMILES (Canonical) CC1C(CCC2(C1CC=C3C2CCC4(C3CCC4C(C)CCCC(C)C)C)C)O
SMILES (Isomeric) C[C@@H]1[C@H](CC[C@]2([C@H]1CC=C3[C@@H]2CC[C@]4([C@H]3CC[C@@H]4[C@H](C)CCCC(C)C)C)C)O
InChI InChI=1S/C28H48O/c1-18(2)8-7-9-19(3)22-12-13-24-21-10-11-23-20(4)26(29)15-17-28(23,6)25(21)14-16-27(22,24)5/h10,18-20,22-26,29H,7-9,11-17H2,1-6H3/t19-,20+,22-,23+,24+,25+,26+,27-,28+/m1/s1
InChI Key LMYZQUNLYGJIHI-SPONXPENSA-N
Popularity 20 references in papers

Physical and Chemical Properties

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Molecular Formula C28H48O
Molecular Weight 400.70 g/mol
Exact Mass 400.370516150 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 8.70
Atomic LogP (AlogP) 7.63
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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481-25-4
Methostenol
4alpha-Methyl-5alpha-cholest-7-en-3beta-ol
4-Methylcholest-7-en-3-ol
UNII-X4BL075LYS
X4BL075LYS
4alpha-methyl-cholest-7-en-3beta-ol
Cholest-7-en-3-ol, 4-methyl-, (3.beta.,4.alpha.,5.alpha.)-
(3S,4S,5S,9R,10S,13R,14R,17R)-4,10,13-trimethyl-17-((R)-6-methylheptan-2-yl)-2,3,4,5,6,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol
4-alpha-Methyl-5-alpha-cholest-7-en-3-beta-ol
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Lophenol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.6678 66.78%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.4911 49.11%
OATP2B1 inhibitior - 0.7271 72.71%
OATP1B1 inhibitior + 0.9078 90.78%
OATP1B3 inhibitior + 0.9592 95.92%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.5938 59.38%
P-glycoprotein inhibitior - 0.5994 59.94%
P-glycoprotein substrate + 0.5875 58.75%
CYP3A4 substrate + 0.6396 63.96%
CYP2C9 substrate - 0.6499 64.99%
CYP2D6 substrate - 0.6843 68.43%
CYP3A4 inhibition - 0.8640 86.40%
CYP2C9 inhibition - 0.8612 86.12%
CYP2C19 inhibition - 0.7681 76.81%
CYP2D6 inhibition - 0.9483 94.83%
CYP1A2 inhibition - 0.9088 90.88%
CYP2C8 inhibition - 0.8779 87.79%
CYP inhibitory promiscuity - 0.5784 57.84%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5998 59.98%
Eye corrosion - 0.9901 99.01%
Eye irritation - 0.9514 95.14%
Skin irritation + 0.6308 63.08%
Skin corrosion - 0.9443 94.43%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.5616 56.16%
skin sensitisation + 0.5785 57.85%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.9375 93.75%
Nephrotoxicity - 0.9113 91.13%
Acute Oral Toxicity (c) III 0.8086 80.86%
Estrogen receptor binding + 0.7641 76.41%
Androgen receptor binding - 0.6849 68.49%
Thyroid receptor binding + 0.7036 70.36%
Glucocorticoid receptor binding + 0.7940 79.40%
Aromatase binding - 0.6467 64.67%
PPAR gamma + 0.5214 52.14%
Honey bee toxicity - 0.8895 88.95%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9890 98.90%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.75% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.95% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.25% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 95.80% 90.17%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 92.07% 82.69%
CHEMBL2581 P07339 Cathepsin D 90.63% 98.95%
CHEMBL3359 P21462 Formyl peptide receptor 1 89.58% 93.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 89.25% 90.71%
CHEMBL2179 P04062 Beta-glucocerebrosidase 89.08% 85.31%
CHEMBL226 P30542 Adenosine A1 receptor 88.74% 95.93%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.39% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.99% 97.09%
CHEMBL4227 P25090 Lipoxin A4 receptor 86.71% 100.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 86.27% 95.89%
CHEMBL237 P41145 Kappa opioid receptor 85.87% 98.10%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.51% 95.89%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.94% 94.45%
CHEMBL1937 Q92769 Histone deacetylase 2 83.46% 94.75%
CHEMBL1871 P10275 Androgen Receptor 82.01% 96.43%
CHEMBL3492 P49721 Proteasome Macropain subunit 80.21% 90.24%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.11% 86.33%

Plants that contains it

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Cross-Links

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PubChem 160482
NPASS NPC171566
LOTUS LTS0271727
wikiData Q27103040