3beta,22beta,24-Trihydroxyoleana-12-ene-30-oic acid gamma-lactone

Details

Top
Internal ID 09ed3e96-20f2-4c8c-b4ee-b34056a8baf7
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (1R,2R,5S,6R,9R,10S,11S,14R,15R,19S,21R)-11-hydroxy-10-(hydroxymethyl)-2,5,6,10,14,21-hexamethyl-23-oxahexacyclo[19.2.1.02,19.05,18.06,15.09,14]tetracos-17-en-22-one
SMILES (Canonical) CC12CCC(C(C1CCC3(C2CC=C4C3(CCC5(C4CC6(CC5OC6=O)C)C)C)C)(C)CO)O
SMILES (Isomeric) C[C@]12CC[C@@H]([C@]([C@@H]1CC[C@@]3([C@@H]2CC=C4[C@]3(CC[C@@]5([C@H]4C[C@@]6(C[C@H]5OC6=O)C)C)C)C)(C)CO)O
InChI InChI=1S/C30H46O4/c1-25-15-19-18-7-8-21-27(3)11-10-22(32)28(4,17-31)20(27)9-12-30(21,6)29(18,5)14-13-26(19,2)23(16-25)34-24(25)33/h7,19-23,31-32H,8-17H2,1-6H3/t19-,20+,21+,22-,23+,25+,26+,27-,28+,29+,30+/m0/s1
InChI Key AXIVEZBRJDDWRQ-ZRZJEJNWSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C30H46O4
Molecular Weight 470.70 g/mol
Exact Mass 470.33960994 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 6.30
Atomic LogP (AlogP) 5.66
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 3beta,22beta,24-Trihydroxyoleana-12-ene-30-oic acid gamma-lactone

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9807 98.07%
Caco-2 - 0.5498 54.98%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.7071 70.71%
OATP2B1 inhibitior - 0.7138 71.38%
OATP1B1 inhibitior + 0.8911 89.11%
OATP1B3 inhibitior + 0.9404 94.04%
MATE1 inhibitior - 0.8612 86.12%
OCT2 inhibitior + 0.5289 52.89%
BSEP inhibitior + 0.8978 89.78%
P-glycoprotein inhibitior - 0.6428 64.28%
P-glycoprotein substrate - 0.7072 70.72%
CYP3A4 substrate + 0.6854 68.54%
CYP2C9 substrate - 0.8086 80.86%
CYP2D6 substrate - 0.8073 80.73%
CYP3A4 inhibition - 0.7159 71.59%
CYP2C9 inhibition - 0.8482 84.82%
CYP2C19 inhibition - 0.9013 90.13%
CYP2D6 inhibition - 0.9436 94.36%
CYP1A2 inhibition - 0.8481 84.81%
CYP2C8 inhibition - 0.6399 63.99%
CYP inhibitory promiscuity - 0.8497 84.97%
UGT catelyzed - 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5437 54.37%
Eye corrosion - 0.9913 99.13%
Eye irritation - 0.9398 93.98%
Skin irritation + 0.5861 58.61%
Skin corrosion - 0.9396 93.96%
Ames mutagenesis - 0.7870 78.70%
Human Ether-a-go-go-Related Gene inhibition - 0.3843 38.43%
Micronuclear - 0.8700 87.00%
Hepatotoxicity - 0.6750 67.50%
skin sensitisation - 0.9043 90.43%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.9778 97.78%
Mitochondrial toxicity + 0.8750 87.50%
Nephrotoxicity + 0.7112 71.12%
Acute Oral Toxicity (c) III 0.6292 62.92%
Estrogen receptor binding + 0.7465 74.65%
Androgen receptor binding + 0.7184 71.84%
Thyroid receptor binding + 0.6391 63.91%
Glucocorticoid receptor binding + 0.8283 82.83%
Aromatase binding + 0.7459 74.59%
PPAR gamma + 0.6465 64.65%
Honey bee toxicity - 0.8634 86.34%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.9804 98.04%

Targets

Top

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
CHEMBL3137262 O60341 LSD1/CoREST complex 93.69% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.67% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.80% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.80% 100.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.28% 97.25%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.65% 95.89%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 83.56% 82.69%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 80.39% 93.00%

Cross-Links

Top
PubChem 102482971
NPASS NPC258867
LOTUS LTS0079849
wikiData Q104920589