3a-(hydroxymethyl)-6-(2-hydroxypropan-2-yl)-8a-methyl-2,3,5,6,7,8-hexahydro-1H-azulen-4-one

Details

Top
Internal ID f99a0922-4300-43f0-b208-440c000f6ea6
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Germacrane sesquiterpenoids
IUPAC Name 3a-(hydroxymethyl)-6-(2-hydroxypropan-2-yl)-8a-methyl-2,3,5,6,7,8-hexahydro-1H-azulen-4-one
SMILES (Canonical) CC12CCCC1(C(=O)CC(CC2)C(C)(C)O)CO
SMILES (Isomeric) CC12CCCC1(C(=O)CC(CC2)C(C)(C)O)CO
InChI InChI=1S/C15H26O3/c1-13(2,18)11-5-8-14(3)6-4-7-15(14,10-16)12(17)9-11/h11,16,18H,4-10H2,1-3H3
InChI Key NVKHSRLHWCUMKO-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C15H26O3
Molecular Weight 254.36 g/mol
Exact Mass 254.18819469 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.30
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 3a-(hydroxymethyl)-6-(2-hydroxypropan-2-yl)-8a-methyl-2,3,5,6,7,8-hexahydro-1H-azulen-4-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9898 98.98%
Caco-2 + 0.8384 83.84%
Blood Brain Barrier + 0.7885 78.85%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.7316 73.16%
OATP2B1 inhibitior - 0.8436 84.36%
OATP1B1 inhibitior + 0.8949 89.49%
OATP1B3 inhibitior + 0.9415 94.15%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6672 66.72%
BSEP inhibitior - 0.7151 71.51%
P-glycoprotein inhibitior - 0.9370 93.70%
P-glycoprotein substrate - 0.8536 85.36%
CYP3A4 substrate + 0.5589 55.89%
CYP2C9 substrate - 0.8472 84.72%
CYP2D6 substrate - 0.8137 81.37%
CYP3A4 inhibition - 0.9064 90.64%
CYP2C9 inhibition - 0.6438 64.38%
CYP2C19 inhibition - 0.8807 88.07%
CYP2D6 inhibition - 0.9586 95.86%
CYP1A2 inhibition - 0.6266 62.66%
CYP2C8 inhibition - 0.8375 83.75%
CYP inhibitory promiscuity - 0.9490 94.90%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.6530 65.30%
Eye corrosion - 0.9815 98.15%
Eye irritation + 0.6044 60.44%
Skin irritation - 0.6827 68.27%
Skin corrosion - 0.9608 96.08%
Ames mutagenesis - 0.8354 83.54%
Human Ether-a-go-go-Related Gene inhibition - 0.8141 81.41%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.5562 55.62%
skin sensitisation - 0.7616 76.16%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity + 0.4567 45.67%
Acute Oral Toxicity (c) III 0.5984 59.84%
Estrogen receptor binding - 0.7853 78.53%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding - 0.6654 66.54%
Glucocorticoid receptor binding - 0.5367 53.67%
Aromatase binding - 0.6377 63.77%
PPAR gamma - 0.7244 72.44%
Honey bee toxicity - 0.9221 92.21%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.8896 88.96%

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 97.86% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.23% 91.11%
CHEMBL2581 P07339 Cathepsin D 94.62% 98.95%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 87.95% 82.69%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 87.92% 93.04%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.43% 97.09%
CHEMBL1937 Q92769 Histone deacetylase 2 86.54% 94.75%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.18% 85.14%
CHEMBL1902 P62942 FK506-binding protein 1A 84.95% 97.05%
CHEMBL5888 Q99558 Mitogen-activated protein kinase kinase kinase 14 84.77% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.71% 95.89%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.69% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.91% 100.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.24% 99.23%
CHEMBL3192 Q9BY41 Histone deacetylase 8 82.12% 93.99%
CHEMBL1871 P10275 Androgen Receptor 81.74% 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.
Chiliadenus montanus

Cross-Links

Top
PubChem 163192703
LOTUS LTS0020244
wikiData Q105186275