(8S,8aS)-3,8-dimethyl-1,4,5,7,8,8a-hexahydroazulene-2,6-dione

Details

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Internal ID 2716575a-c543-40b9-bc6a-6ab1f68ecd20
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones
IUPAC Name (8S,8aS)-3,8-dimethyl-1,4,5,7,8,8a-hexahydroazulene-2,6-dione
SMILES (Canonical) CC1CC(=O)CCC2=C(C(=O)CC12)C
SMILES (Isomeric) C[C@H]1CC(=O)CCC2=C(C(=O)C[C@@H]12)C
InChI InChI=1S/C12H16O2/c1-7-5-9(13)3-4-10-8(2)12(14)6-11(7)10/h7,11H,3-6H2,1-2H3/t7-,11-/m0/s1
InChI Key YHSGXZITHLPVHN-CPCISQLKSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H16O2
Molecular Weight 192.25 g/mol
Exact Mass 192.115029749 g/mol
Topological Polar Surface Area (TPSA) 34.10 Ų
XlogP 0.80
Atomic LogP (AlogP) 2.28
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (8S,8aS)-3,8-dimethyl-1,4,5,7,8,8a-hexahydroazulene-2,6-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9971 99.71%
Caco-2 + 0.7860 78.60%
Blood Brain Barrier + 0.7580 75.80%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.5864 58.64%
OATP2B1 inhibitior - 0.8434 84.34%
OATP1B1 inhibitior + 0.9508 95.08%
OATP1B3 inhibitior + 0.9697 96.97%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior - 0.8812 88.12%
P-glycoprotein inhibitior - 0.9483 94.83%
P-glycoprotein substrate - 0.9022 90.22%
CYP3A4 substrate - 0.5473 54.73%
CYP2C9 substrate - 0.8170 81.70%
CYP2D6 substrate - 0.8598 85.98%
CYP3A4 inhibition - 0.9252 92.52%
CYP2C9 inhibition - 0.8955 89.55%
CYP2C19 inhibition - 0.8554 85.54%
CYP2D6 inhibition - 0.9186 91.86%
CYP1A2 inhibition - 0.6294 62.94%
CYP2C8 inhibition - 0.9477 94.77%
CYP inhibitory promiscuity - 0.9001 90.01%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5437 54.37%
Eye corrosion - 0.9458 94.58%
Eye irritation + 0.8068 80.68%
Skin irritation + 0.5360 53.60%
Skin corrosion - 0.9458 94.58%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4044 40.44%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation + 0.7238 72.38%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity + 0.5291 52.91%
Acute Oral Toxicity (c) III 0.6791 67.91%
Estrogen receptor binding - 0.9014 90.14%
Androgen receptor binding - 0.6622 66.22%
Thyroid receptor binding - 0.8438 84.38%
Glucocorticoid receptor binding - 0.9119 91.19%
Aromatase binding - 0.8678 86.78%
PPAR gamma - 0.8410 84.10%
Honey bee toxicity - 0.8885 88.85%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity + 0.9753 97.53%

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 91.34% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.53% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.84% 96.09%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.16% 90.71%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.75% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.51% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.43% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.32% 99.23%

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.
Pechuel-loeschea leubnitziae

Cross-Links

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PubChem 163012461
LOTUS LTS0226216
wikiData Q105348581