1-Methyl-4-methylidene-7-propan-2-yl-3,5,6,7,8,8a-hexahydroazulen-3a-ol

Details

Top
Internal ID 29929bfc-732b-45d2-b8a1-e7d3d5292049
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Guaianes
IUPAC Name 1-methyl-4-methylidene-7-propan-2-yl-3,5,6,7,8,8a-hexahydroazulen-3a-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O/c1-10(2)13-6-5-12(4)15(16)8-7-11(3)14(15)9-13/h7,10,13-14,16H,4-6,8-9H2,1-3H3
InChI Key FUIREXPFHXOXGQ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H24O
Molecular Weight 220.35 g/mol
Exact Mass 220.182715385 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.00
Atomic LogP (AlogP) 3.70
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 1-Methyl-4-methylidene-7-propan-2-yl-3,5,6,7,8,8a-hexahydroazulen-3a-ol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9941 99.41%
Caco-2 + 0.6267 62.67%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Lysosomes 0.5988 59.88%
OATP2B1 inhibitior - 0.8510 85.10%
OATP1B1 inhibitior + 0.9358 93.58%
OATP1B3 inhibitior + 0.8025 80.25%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.7617 76.17%
P-glycoprotein inhibitior - 0.9079 90.79%
P-glycoprotein substrate - 0.8229 82.29%
CYP3A4 substrate - 0.5069 50.69%
CYP2C9 substrate - 0.5471 54.71%
CYP2D6 substrate - 0.7267 72.67%
CYP3A4 inhibition - 0.9230 92.30%
CYP2C9 inhibition - 0.7560 75.60%
CYP2C19 inhibition - 0.7406 74.06%
CYP2D6 inhibition - 0.9368 93.68%
CYP1A2 inhibition - 0.7207 72.07%
CYP2C8 inhibition - 0.8926 89.26%
CYP inhibitory promiscuity - 0.8661 86.61%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.6099 60.99%
Eye corrosion - 0.9675 96.75%
Eye irritation - 0.5727 57.27%
Skin irritation + 0.6739 67.39%
Skin corrosion - 0.9380 93.80%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5221 52.21%
Micronuclear - 0.9400 94.00%
Hepatotoxicity + 0.5649 56.49%
skin sensitisation + 0.5654 56.54%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity - 0.7316 73.16%
Acute Oral Toxicity (c) III 0.7622 76.22%
Estrogen receptor binding - 0.8710 87.10%
Androgen receptor binding - 0.6107 61.07%
Thyroid receptor binding - 0.5466 54.66%
Glucocorticoid receptor binding - 0.6452 64.52%
Aromatase binding - 0.8516 85.16%
PPAR gamma - 0.8008 80.08%
Honey bee toxicity - 0.8943 89.43%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9586 95.86%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.74% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.15% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.86% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.65% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.89% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.13% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.80% 100.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.81% 93.04%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.70% 93.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.31% 94.45%
CHEMBL1871 P10275 Androgen Receptor 80.19% 96.43%

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.
Cleome droserifolia

Cross-Links

Top
PubChem 163063293
LOTUS LTS0143341
wikiData Q105001751