Lanosta-7,9(11)-diene-12beta,21alpha-epoxy-2alpha,3beta,24beta,25-tetraol

Details

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Internal ID 002d5cb6-98d8-4916-bed1-853692bdecf9
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (1S,5R,7R,8R,10S,13R,16R,17R,20R)-16-[(3R)-3,4-dihydroxy-4-methylpentyl]-1,6,6,10,20-pentamethyl-14-oxapentacyclo[11.6.1.02,11.05,10.017,20]icosa-2,11-diene-7,8-diol
SMILES (Canonical) CC1(C2CC=C3C(=CC4C5(C3(CCC5C(CO4)CCC(C(C)(C)O)O)C)C)C2(CC(C1O)O)C)C
SMILES (Isomeric) C[C@@]12CC[C@H]3[C@]1([C@@H](C=C4C2=CC[C@@H]5[C@@]4(C[C@H]([C@@H](C5(C)C)O)O)C)OC[C@@H]3CC[C@H](C(C)(C)O)O)C
InChI InChI=1S/C30H48O5/c1-26(2)22-10-9-19-20(28(22,5)15-21(31)25(26)33)14-24-30(7)18(12-13-29(19,30)6)17(16-35-24)8-11-23(32)27(3,4)34/h9,14,17-18,21-25,31-34H,8,10-13,15-16H2,1-7H3/t17-,18+,21+,22-,23+,24+,25-,28+,29-,30-/m0/s1
InChI Key ZORFRMPXGZTBKI-NGRKGBKKSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C30H48O5
Molecular Weight 488.70 g/mol
Exact Mass 488.35017463 g/mol
Topological Polar Surface Area (TPSA) 90.20 Ų
XlogP 3.80
Atomic LogP (AlogP) 4.38
H-Bond Acceptor 5
H-Bond Donor 4
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Lanosta-7,9(11)-diene-12beta,21alpha-epoxy-2alpha,3beta,24beta,25-tetraol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9711 97.11%
Caco-2 + 0.5130 51.30%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.7897 78.97%
OATP2B1 inhibitior - 0.8606 86.06%
OATP1B1 inhibitior + 0.8636 86.36%
OATP1B3 inhibitior + 0.9672 96.72%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6292 62.92%
BSEP inhibitior - 0.6255 62.55%
P-glycoprotein inhibitior - 0.5279 52.79%
P-glycoprotein substrate + 0.5573 55.73%
CYP3A4 substrate + 0.7020 70.20%
CYP2C9 substrate - 0.7962 79.62%
CYP2D6 substrate - 0.7878 78.78%
CYP3A4 inhibition - 0.8481 84.81%
CYP2C9 inhibition - 0.8647 86.47%
CYP2C19 inhibition - 0.8839 88.39%
CYP2D6 inhibition - 0.9255 92.55%
CYP1A2 inhibition - 0.8662 86.62%
CYP2C8 inhibition + 0.6488 64.88%
CYP inhibitory promiscuity - 0.8967 89.67%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6818 68.18%
Eye corrosion - 0.9913 99.13%
Eye irritation - 0.9475 94.75%
Skin irritation - 0.5256 52.56%
Skin corrosion - 0.9438 94.38%
Ames mutagenesis - 0.7078 70.78%
Human Ether-a-go-go-Related Gene inhibition + 0.6929 69.29%
Micronuclear - 0.8900 89.00%
Hepatotoxicity - 0.6343 63.43%
skin sensitisation - 0.8283 82.83%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.8283 82.83%
Acute Oral Toxicity (c) III 0.5972 59.72%
Estrogen receptor binding + 0.7660 76.60%
Androgen receptor binding + 0.7165 71.65%
Thyroid receptor binding + 0.6753 67.53%
Glucocorticoid receptor binding + 0.7382 73.82%
Aromatase binding + 0.6886 68.86%
PPAR gamma + 0.5833 58.33%
Honey bee toxicity - 0.7241 72.41%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9603 96.03%

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 99.11% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.78% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.48% 96.09%
CHEMBL2581 P07339 Cathepsin D 94.46% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.80% 97.09%
CHEMBL2996 Q05655 Protein kinase C delta 92.13% 97.79%
CHEMBL1994 P08235 Mineralocorticoid receptor 91.10% 100.00%
CHEMBL218 P21554 Cannabinoid CB1 receptor 89.87% 96.61%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 88.86% 97.14%
CHEMBL226 P30542 Adenosine A1 receptor 87.97% 95.93%
CHEMBL3359 P21462 Formyl peptide receptor 1 85.56% 93.56%
CHEMBL4227 P25090 Lipoxin A4 receptor 84.63% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.27% 89.00%
CHEMBL4662 P28074 Proteasome Macropain subunit MB1 82.29% 93.85%
CHEMBL2094135 Q96BI3 Gamma-secretase 82.01% 98.05%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 81.73% 82.69%
CHEMBL4581 P52732 Kinesin-like protein 1 81.23% 93.18%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.17% 86.33%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 80.64% 94.78%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.24% 100.00%

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 146682658
LOTUS LTS0204532
wikiData Q105380659