24-Methylenelophenol

Details

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Internal ID 637f95a2-2fe2-4351-9dd5-8b6a8527facb
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Ergostane steroids > Ergosterols and derivatives
IUPAC Name (3S,4S,5S,9R,10S,13R,14R,17R)-4,10,13-trimethyl-17-[(2R)-6-methyl-5-methylideneheptan-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)CCC(=C)C(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)CCC(=C)C(C)C)C)C)O
InChI InChI=1S/C29H48O/c1-18(2)19(3)8-9-20(4)23-12-13-25-22-10-11-24-21(5)27(30)15-17-29(24,7)26(22)14-16-28(23,25)6/h10,18,20-21,23-27,30H,3,8-9,11-17H2,1-2,4-7H3/t20-,21+,23-,24+,25+,26+,27+,28-,29+/m1/s1
InChI Key RSMKYRDCCSNYFM-AAGDOFLISA-N
Popularity 15 references in papers

Physical and Chemical Properties

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Molecular Formula C29H48O
Molecular Weight 412.70 g/mol
Exact Mass 412.370516150 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 8.80
Atomic LogP (AlogP) 7.80
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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Gramisterol
Gramisterin
24-methylidenelophenol
1176-52-9
Lophenol, 24-methylene-
(3S,4S,5S,9R,10S,13R,14R,17R)-4,10,13-trimethyl-17-[(2R)-6-methyl-5-methylideneheptan-2-yl]-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol
4alpha-methyl,24-methylene-cholest-7-en-3beta-ol
4alpha-Methyl-24-methylene-5alpha-cholest-7-en-3beta-ol
Ergosta-7,24(28)-dien-3-ol, 4-methyl-, (3.beta.,4.alpha.,5.alpha.)-
4alpha-Methylepisterol
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 24-Methylenelophenol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9971 99.71%
Caco-2 + 0.6129 61.29%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Lysosomes 0.4702 47.02%
OATP2B1 inhibitior - 0.5867 58.67%
OATP1B1 inhibitior + 0.8506 85.06%
OATP1B3 inhibitior + 0.8637 86.37%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.6772 67.72%
P-glycoprotein inhibitior - 0.5401 54.01%
P-glycoprotein substrate - 0.5735 57.35%
CYP3A4 substrate + 0.6431 64.31%
CYP2C9 substrate - 0.6499 64.99%
CYP2D6 substrate - 0.6843 68.43%
CYP3A4 inhibition - 0.8499 84.99%
CYP2C9 inhibition - 0.8492 84.92%
CYP2C19 inhibition - 0.7480 74.80%
CYP2D6 inhibition - 0.9460 94.60%
CYP1A2 inhibition - 0.9054 90.54%
CYP2C8 inhibition - 0.8064 80.64%
CYP inhibitory promiscuity - 0.6154 61.54%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6245 62.45%
Eye corrosion - 0.9884 98.84%
Eye irritation - 0.9558 95.58%
Skin irritation + 0.5935 59.35%
Skin corrosion - 0.9398 93.98%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5279 52.79%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.5890 58.90%
skin sensitisation + 0.5493 54.93%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.9444 94.44%
Mitochondrial toxicity + 0.9375 93.75%
Nephrotoxicity - 0.8738 87.38%
Acute Oral Toxicity (c) III 0.8414 84.14%
Estrogen receptor binding + 0.7326 73.26%
Androgen receptor binding - 0.7353 73.53%
Thyroid receptor binding + 0.7093 70.93%
Glucocorticoid receptor binding + 0.8029 80.29%
Aromatase binding - 0.6065 60.65%
PPAR gamma + 0.5859 58.59%
Honey bee toxicity - 0.7893 78.93%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.9947 99.47%

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 99.24% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.09% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.19% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 96.12% 90.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.44% 97.09%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 90.41% 82.69%
CHEMBL2581 P07339 Cathepsin D 90.16% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.91% 100.00%
CHEMBL218 P21554 Cannabinoid CB1 receptor 87.30% 96.61%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.97% 95.89%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 85.76% 95.89%
CHEMBL237 P41145 Kappa opioid receptor 84.84% 98.10%
CHEMBL3492 P49721 Proteasome Macropain subunit 84.76% 90.24%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.70% 90.71%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 83.63% 89.05%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.33% 93.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.28% 94.45%
CHEMBL4227 P25090 Lipoxin A4 receptor 82.71% 100.00%
CHEMBL1871 P10275 Androgen Receptor 82.14% 96.43%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.69% 92.62%

Cross-Links

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PubChem 5283640
NPASS NPC46213
LOTUS LTS0024189
wikiData Q27104062