24-Methylene,25-methylcholesta-5-en-3beta-ol

Details

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Internal ID 242d08d5-d438-4bc5-bc0c-5e229f3e5ea6
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Ergostane steroids > Ergosterols and derivatives
IUPAC Name (3S,8S,9S,10R,13R,14S,17R)-17-[(2R)-6,6-dimethyl-5-methylideneheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol
SMILES (Canonical) CC(CCC(=C)C(C)(C)C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C
SMILES (Isomeric) C[C@H](CCC(=C)C(C)(C)C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC=C4[C@@]3(CC[C@@H](C4)O)C)C
InChI InChI=1S/C29H48O/c1-19(8-9-20(2)27(3,4)5)24-12-13-25-23-11-10-21-18-22(30)14-16-28(21,6)26(23)15-17-29(24,25)7/h10,19,22-26,30H,2,8-9,11-18H2,1,3-7H3/t19-,22+,23+,24-,25+,26+,28+,29-/m1/s1
InChI Key QXDHYSHOINNEAZ-HSIBUNQISA-N
Popularity 14 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 9.20
Atomic LogP (AlogP) 7.94
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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24-methylene,25-methylcholesta-5-en-3beta-ol
LMST01030104
SCHEMBL1545877
DTXSID001275426
(3beta)-25-Methylergosta-5,24(28)-dien-3-ol
89702-24-9

2D Structure

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2D Structure of 24-Methylene,25-methylcholesta-5-en-3beta-ol

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 + 0.5569 55.69%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Lysosomes 0.4567 45.67%
OATP2B1 inhibitior - 0.5910 59.10%
OATP1B1 inhibitior + 0.9230 92.30%
OATP1B3 inhibitior + 0.8121 81.21%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.8709 87.09%
P-glycoprotein inhibitior - 0.4918 49.18%
P-glycoprotein substrate + 0.7713 77.13%
CYP3A4 substrate + 0.7489 74.89%
CYP2C9 substrate - 0.6499 64.99%
CYP2D6 substrate - 0.6843 68.43%
CYP3A4 inhibition - 0.8417 84.17%
CYP2C9 inhibition - 0.9061 90.61%
CYP2C19 inhibition - 0.8966 89.66%
CYP2D6 inhibition - 0.9489 94.89%
CYP1A2 inhibition - 0.9282 92.82%
CYP2C8 inhibition + 0.5328 53.28%
CYP inhibitory promiscuity - 0.7021 70.21%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6136 61.36%
Eye corrosion - 0.9871 98.71%
Eye irritation - 0.9533 95.33%
Skin irritation + 0.5493 54.93%
Skin corrosion - 0.9461 94.61%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6759 67.59%
Micronuclear - 0.9500 95.00%
Hepatotoxicity + 0.6167 61.67%
skin sensitisation + 0.6283 62.83%
Respiratory toxicity + 0.8889 88.89%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity - 0.7885 78.85%
Acute Oral Toxicity (c) I 0.7707 77.07%
Estrogen receptor binding + 0.8708 87.08%
Androgen receptor binding + 0.8294 82.94%
Thyroid receptor binding + 0.6905 69.05%
Glucocorticoid receptor binding + 0.8019 80.19%
Aromatase binding + 0.5313 53.13%
PPAR gamma + 0.5843 58.43%
Honey bee toxicity - 0.7271 72.71%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9939 99.39%

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 99.03% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.51% 96.09%
CHEMBL2581 P07339 Cathepsin D 95.18% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.84% 91.11%
CHEMBL226 P30542 Adenosine A1 receptor 92.45% 95.93%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.61% 94.45%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 90.33% 95.89%
CHEMBL2094135 Q96BI3 Gamma-secretase 89.15% 98.05%
CHEMBL3359 P21462 Formyl peptide receptor 1 88.79% 93.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.46% 100.00%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 88.27% 89.05%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.83% 90.71%
CHEMBL3242 O43570 Carbonic anhydrase XII 85.58% 97.37%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.48% 97.09%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 84.64% 96.90%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 84.41% 97.23%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.50% 95.89%
CHEMBL4227 P25090 Lipoxin A4 receptor 83.16% 100.00%
CHEMBL238 Q01959 Dopamine transporter 82.35% 95.88%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 82.00% 82.69%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 81.08% 98.33%
CHEMBL2007625 O75874 Isocitrate dehydrogenase [NADP] cytoplasmic 81.03% 99.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.83% 93.04%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.48% 86.33%
CHEMBL237 P41145 Kappa opioid receptor 80.21% 98.10%
CHEMBL2959 Q08881 Tyrosine-protein kinase ITK/TSK 80.15% 95.00%

Plants that contains it

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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.
Brassica juncea
Dioscorea polystachya
Fritillaria pallidiflora
Kalanchoe daigremontiana
Kalanchoe marmorata
Koelreuteria paniculata
Phaseolus vulgaris
Wrightia tinctoria

Cross-Links

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PubChem 5283645
NPASS NPC32710
LOTUS LTS0200547
wikiData Q76294346