1,2-Dihydroxybisabola-3,10-Diene

Details

Top
Internal ID 343c692f-b2ab-4e28-9ede-0a457d694420
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 3-methyl-6-(6-methylhept-5-en-2-yl)cyclohex-3-ene-1,2-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H26O2/c1-10(2)6-5-7-11(3)13-9-8-12(4)14(16)15(13)17/h6,8,11,13-17H,5,7,9H2,1-4H3
InChI Key SDAWXTDBEYZMMX-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H26O2
Molecular Weight 238.37 g/mol
Exact Mass 238.193280068 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 3.10
Atomic LogP (AlogP) 3.06
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

Top
RefChem:71941
3-methyl-6-(6-methylhept-5-en-2-yl)cyclohex-3-ene-1,2-diol
CHEBI:67819
CHEMBL1775015
Q27136295
6-(1,5-dimethylhex-4-enyl)-3-methyl-cyclohex-3-ene-1,2-diol

2D Structure

Top
2D Structure of 1,2-Dihydroxybisabola-3,10-Diene

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9852 98.52%
Caco-2 + 0.7847 78.47%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.7270 72.70%
OATP2B1 inhibitior - 0.8531 85.31%
OATP1B1 inhibitior + 0.9256 92.56%
OATP1B3 inhibitior + 0.9405 94.05%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.8687 86.87%
P-glycoprotein inhibitior - 0.9590 95.90%
P-glycoprotein substrate - 0.8128 81.28%
CYP3A4 substrate - 0.6076 60.76%
CYP2C9 substrate - 0.8066 80.66%
CYP2D6 substrate - 0.7282 72.82%
CYP3A4 inhibition - 0.7214 72.14%
CYP2C9 inhibition - 0.6962 69.62%
CYP2C19 inhibition - 0.7097 70.97%
CYP2D6 inhibition - 0.8036 80.36%
CYP1A2 inhibition - 0.7153 71.53%
CYP2C8 inhibition - 0.9798 97.98%
CYP inhibitory promiscuity - 0.6680 66.80%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.6579 65.79%
Eye corrosion - 0.9336 93.36%
Eye irritation - 0.9076 90.76%
Skin irritation - 0.5582 55.82%
Skin corrosion - 0.9118 91.18%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6215 62.15%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation + 0.7537 75.37%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity + 0.4602 46.02%
Acute Oral Toxicity (c) III 0.6860 68.60%
Estrogen receptor binding - 0.8460 84.60%
Androgen receptor binding - 0.7216 72.16%
Thyroid receptor binding - 0.6295 62.95%
Glucocorticoid receptor binding - 0.5526 55.26%
Aromatase binding - 0.9138 91.38%
PPAR gamma - 0.7182 71.82%
Honey bee toxicity - 0.9327 93.27%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.9882 98.82%

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
CHEMBL2581 P07339 Cathepsin D 93.39% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.13% 96.09%
CHEMBL3359 P21462 Formyl peptide receptor 1 90.63% 93.56%
CHEMBL3401 O75469 Pregnane X receptor 88.57% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.44% 91.11%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.28% 90.71%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.63% 94.45%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.55% 97.25%
CHEMBL221 P23219 Cyclooxygenase-1 83.33% 90.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.21% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.70% 100.00%

Plants that contains it

Top
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.
Cupania cinerea

Cross-Links

Top
PubChem 52951624
NPASS NPC326310
ChEMBL CHEMBL1775015