(6R,8S,8aR)-6-hydroxy-3,8-dimethyl-5-propan-2-yl-6,7,8,8a-tetrahydro-1H-azulen-2-one

Details

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Internal ID 8f1777bf-85a6-4910-b04a-8aba32b18748
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Guaianes
IUPAC Name (6R,8S,8aR)-6-hydroxy-3,8-dimethyl-5-propan-2-yl-6,7,8,8a-tetrahydro-1H-azulen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H22O2/c1-8(2)11-6-13-10(4)14(16)7-12(13)9(3)5-15(11)17/h6,8-9,12,15,17H,5,7H2,1-4H3/t9-,12+,15+/m0/s1
InChI Key CYDOPCBUSSJNHM-TURKWSHLSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O2
Molecular Weight 234.33 g/mol
Exact Mass 234.161979940 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 1.80
Atomic LogP (AlogP) 2.88
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (6R,8S,8aR)-6-hydroxy-3,8-dimethyl-5-propan-2-yl-6,7,8,8a-tetrahydro-1H-azulen-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.9033 90.33%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.5435 54.35%
OATP2B1 inhibitior - 0.8561 85.61%
OATP1B1 inhibitior + 0.9326 93.26%
OATP1B3 inhibitior + 0.9682 96.82%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.8902 89.02%
P-glycoprotein inhibitior - 0.9350 93.50%
P-glycoprotein substrate - 0.7761 77.61%
CYP3A4 substrate - 0.5274 52.74%
CYP2C9 substrate - 0.7636 76.36%
CYP2D6 substrate - 0.8540 85.40%
CYP3A4 inhibition - 0.8430 84.30%
CYP2C9 inhibition - 0.8902 89.02%
CYP2C19 inhibition - 0.8572 85.72%
CYP2D6 inhibition - 0.9239 92.39%
CYP1A2 inhibition - 0.7137 71.37%
CYP2C8 inhibition - 0.9358 93.58%
CYP inhibitory promiscuity - 0.9086 90.86%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8717 87.17%
Carcinogenicity (trinary) Non-required 0.5535 55.35%
Eye corrosion - 0.9588 95.88%
Eye irritation - 0.7933 79.33%
Skin irritation + 0.5608 56.08%
Skin corrosion - 0.9266 92.66%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5572 55.72%
Micronuclear - 0.8941 89.41%
Hepatotoxicity + 0.6584 65.84%
skin sensitisation + 0.6280 62.80%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.6540 65.40%
Acute Oral Toxicity (c) III 0.6534 65.34%
Estrogen receptor binding - 0.8410 84.10%
Androgen receptor binding - 0.5491 54.91%
Thyroid receptor binding + 0.5378 53.78%
Glucocorticoid receptor binding - 0.6991 69.91%
Aromatase binding - 0.8572 85.72%
PPAR gamma - 0.7578 75.78%
Honey bee toxicity - 0.8983 89.83%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9485 94.85%

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
CHEMBL2581 P07339 Cathepsin D 94.09% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.49% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.36% 96.09%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 89.99% 90.71%
CHEMBL3359 P21462 Formyl peptide receptor 1 84.69% 93.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.25% 85.14%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.95% 97.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.83% 99.23%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 83.36% 93.65%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 82.09% 86.00%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 81.09% 100.00%

Plants that contains it

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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.
Christiana africana

Cross-Links

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PubChem 163069155
LOTUS LTS0248917
wikiData Q104972256