1-methyl-4-methylidene-7-propan-2-yl-2,3,3a,5,6,8a-hexahydro-1H-azulene

Details

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Internal ID a7d8693b-5a74-4037-af68-33632c008cb5
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Guaianes
IUPAC Name 1-methyl-4-methylidene-7-propan-2-yl-2,3,3a,5,6,8a-hexahydro-1H-azulene
SMILES (Canonical) CC1CCC2C1C=C(CCC2=C)C(C)C
SMILES (Isomeric) CC1CCC2C1C=C(CCC2=C)C(C)C
InChI InChI=1S/C15H24/c1-10(2)13-7-5-11(3)14-8-6-12(4)15(14)9-13/h9-10,12,14-15H,3,5-8H2,1-2,4H3
InChI Key QCESRPKOTSPFAU-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24
Molecular Weight 204.35 g/mol
Exact Mass 204.187800766 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.30
Atomic LogP (AlogP) 4.58
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-methyl-4-methylidene-7-propan-2-yl-2,3,3a,5,6,8a-hexahydro-1H-azulene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9923 99.23%
Caco-2 + 0.8918 89.18%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Lysosomes 0.5845 58.45%
OATP2B1 inhibitior - 0.8484 84.84%
OATP1B1 inhibitior + 0.8735 87.35%
OATP1B3 inhibitior + 0.9446 94.46%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.9287 92.87%
P-glycoprotein inhibitior - 0.8726 87.26%
P-glycoprotein substrate - 0.8569 85.69%
CYP3A4 substrate - 0.5429 54.29%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.6973 69.73%
CYP3A4 inhibition - 0.9526 95.26%
CYP2C9 inhibition - 0.7702 77.02%
CYP2C19 inhibition - 0.7476 74.76%
CYP2D6 inhibition - 0.9247 92.47%
CYP1A2 inhibition - 0.6192 61.92%
CYP2C8 inhibition - 0.8700 87.00%
CYP inhibitory promiscuity - 0.7975 79.75%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7200 72.00%
Carcinogenicity (trinary) Non-required 0.4640 46.40%
Eye corrosion - 0.7932 79.32%
Eye irritation + 0.6116 61.16%
Skin irritation + 0.6366 63.66%
Skin corrosion - 0.9738 97.38%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6668 66.68%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation + 0.8370 83.70%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.7111 71.11%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.7330 73.30%
Acute Oral Toxicity (c) III 0.8514 85.14%
Estrogen receptor binding - 0.9069 90.69%
Androgen receptor binding - 0.6302 63.02%
Thyroid receptor binding - 0.6334 63.34%
Glucocorticoid receptor binding - 0.7177 71.77%
Aromatase binding - 0.8114 81.14%
PPAR gamma - 0.8997 89.97%
Honey bee toxicity - 0.8714 87.14%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.6800 68.00%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.12% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.05% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.45% 96.09%
CHEMBL2581 P07339 Cathepsin D 88.28% 98.95%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 87.73% 97.23%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.18% 97.09%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 85.53% 94.80%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.31% 93.56%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 80.25% 93.40%
CHEMBL226 P30542 Adenosine A1 receptor 80.12% 95.93%

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.
Commiphora gileadensis
Cupressus macrocarpa

Cross-Links

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PubChem 73194711
LOTUS LTS0138413
wikiData Q104195679