(3beta,9xi,10xi)-24-Methylene-9,19-cyclolanostan-3-ol

Details

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Internal ID 5707ca2a-87ea-4a74-ae7d-6989a2566a40
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Cycloartanols and derivatives
IUPAC Name (6S,8R,11S,12S,15R,16R)-7,7,12,16-tetramethyl-15-(6-methyl-5-methylideneheptan-2-yl)pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol
SMILES (Canonical) CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C
SMILES (Isomeric) CC(C)C(=C)CCC(C)[C@H]1CC[C@@]2([C@@]1(CCC34[C@H]2CC[C@@H]5C3(C4)CC[C@@H](C5(C)C)O)C)C
InChI InChI=1S/C31H52O/c1-20(2)21(3)9-10-22(4)23-13-15-29(8)25-12-11-24-27(5,6)26(32)14-16-30(24)19-31(25,30)18-17-28(23,29)7/h20,22-26,32H,3,9-19H2,1-2,4-8H3/t22?,23-,24+,25+,26+,28-,29+,30?,31?/m1/s1
InChI Key BDHQMRXFDYJGII-KFPXMFSNSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C31H52O
Molecular Weight 440.70 g/mol
Exact Mass 440.401816278 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 10.30
Atomic LogP (AlogP) 8.41
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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(3beta,9xi,10xi)-24-Methylene-9,19-cyclolanostan-3-ol

2D Structure

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2D Structure of (3beta,9xi,10xi)-24-Methylene-9,19-cyclolanostan-3-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9960 99.60%
Caco-2 - 0.5238 52.38%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Lysosomes 0.5504 55.04%
OATP2B1 inhibitior - 0.5758 57.58%
OATP1B1 inhibitior + 0.8938 89.38%
OATP1B3 inhibitior + 0.8339 83.39%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.6825 68.25%
P-glycoprotein inhibitior - 0.6300 63.00%
P-glycoprotein substrate - 0.7118 71.18%
CYP3A4 substrate + 0.6278 62.78%
CYP2C9 substrate - 0.6284 62.84%
CYP2D6 substrate - 0.6829 68.29%
CYP3A4 inhibition - 0.8015 80.15%
CYP2C9 inhibition - 0.7064 70.64%
CYP2C19 inhibition - 0.7285 72.85%
CYP2D6 inhibition - 0.9424 94.24%
CYP1A2 inhibition - 0.8045 80.45%
CYP2C8 inhibition - 0.6919 69.19%
CYP inhibitory promiscuity - 0.6252 62.52%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.6425 64.25%
Eye corrosion - 0.9871 98.71%
Eye irritation - 0.8933 89.33%
Skin irritation + 0.5384 53.84%
Skin corrosion - 0.9361 93.61%
Ames mutagenesis - 0.8065 80.65%
Human Ether-a-go-go-Related Gene inhibition - 0.4616 46.16%
Micronuclear - 0.9100 91.00%
Hepatotoxicity - 0.6593 65.93%
skin sensitisation + 0.5312 53.12%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.9375 93.75%
Nephrotoxicity - 0.8002 80.02%
Acute Oral Toxicity (c) III 0.7744 77.44%
Estrogen receptor binding + 0.8115 81.15%
Androgen receptor binding + 0.7471 74.71%
Thyroid receptor binding + 0.6287 62.87%
Glucocorticoid receptor binding + 0.7974 79.74%
Aromatase binding + 0.6952 69.52%
PPAR gamma + 0.5877 58.77%
Honey bee toxicity - 0.7111 71.11%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5800 58.00%
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 98.63% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.23% 91.11%
CHEMBL240 Q12809 HERG 94.67% 89.76%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.50% 96.09%
CHEMBL218 P21554 Cannabinoid CB1 receptor 93.63% 96.61%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.01% 97.09%
CHEMBL3837 P07711 Cathepsin L 90.87% 96.61%
CHEMBL2581 P07339 Cathepsin D 90.20% 98.95%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 88.89% 95.58%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 88.13% 95.17%
CHEMBL3492 P49721 Proteasome Macropain subunit 87.91% 90.24%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.90% 94.45%
CHEMBL233 P35372 Mu opioid receptor 86.33% 97.93%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 85.36% 93.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.85% 92.62%
CHEMBL237 P41145 Kappa opioid receptor 83.90% 98.10%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.71% 100.00%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 83.67% 89.05%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 83.11% 94.78%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 83.09% 95.50%
CHEMBL206 P03372 Estrogen receptor alpha 82.71% 97.64%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 82.66% 82.69%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.05% 95.89%
CHEMBL4227 P25090 Lipoxin A4 receptor 81.72% 100.00%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 81.53% 98.75%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 80.97% 92.86%
CHEMBL2996 Q05655 Protein kinase C delta 80.81% 97.79%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 80.20% 91.03%

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.
Euphorbia ebracteolata
Euphorbia fischeriana
Hippophae rhamnoides
Melia azedarach
Sparganium stoloniferum

Cross-Links

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PubChem 5273649
NPASS NPC159670