1-Methyl-7-propan-2-yl-3,3a,6,7,8,8a-hexahydroazulene-4-carboxylic acid

Details

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Internal ID 383448b9-3b00-4f01-bdf9-1b1f1b277a8d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Guaianes
IUPAC Name 1-methyl-7-propan-2-yl-3,3a,6,7,8,8a-hexahydroazulene-4-carboxylic acid
SMILES (Canonical) CC1=CCC2C1CC(CC=C2C(=O)O)C(C)C
SMILES (Isomeric) CC1=CCC2C1CC(CC=C2C(=O)O)C(C)C
InChI InChI=1S/C15H22O2/c1-9(2)11-5-7-13(15(16)17)12-6-4-10(3)14(12)8-11/h4,7,9,11-12,14H,5-6,8H2,1-3H3,(H,16,17)
InChI Key DFXLQBQZXVPYFY-UHFFFAOYSA-N
Popularity 0 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 3.40
Atomic LogP (AlogP) 3.65
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-Methyl-7-propan-2-yl-3,3a,6,7,8,8a-hexahydroazulene-4-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9955 99.55%
Caco-2 + 0.7089 70.89%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Lysosomes 0.3945 39.45%
OATP2B1 inhibitior - 0.8567 85.67%
OATP1B1 inhibitior + 0.9211 92.11%
OATP1B3 inhibitior + 0.9094 90.94%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.7895 78.95%
P-glycoprotein inhibitior - 0.9485 94.85%
P-glycoprotein substrate - 0.8622 86.22%
CYP3A4 substrate - 0.5967 59.67%
CYP2C9 substrate - 0.5618 56.18%
CYP2D6 substrate - 0.9140 91.40%
CYP3A4 inhibition - 0.9236 92.36%
CYP2C9 inhibition - 0.7592 75.92%
CYP2C19 inhibition - 0.8136 81.36%
CYP2D6 inhibition - 0.9302 93.02%
CYP1A2 inhibition - 0.7718 77.18%
CYP2C8 inhibition - 0.9147 91.47%
CYP inhibitory promiscuity - 0.9042 90.42%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7517 75.17%
Carcinogenicity (trinary) Non-required 0.6581 65.81%
Eye corrosion - 0.7970 79.70%
Eye irritation - 0.6017 60.17%
Skin irritation + 0.5466 54.66%
Skin corrosion - 0.9440 94.40%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5621 56.21%
Micronuclear - 0.8841 88.41%
Hepatotoxicity - 0.5662 56.62%
skin sensitisation + 0.5931 59.31%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity - 0.6291 62.91%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity - 0.8064 80.64%
Acute Oral Toxicity (c) III 0.7700 77.00%
Estrogen receptor binding - 0.8383 83.83%
Androgen receptor binding - 0.6148 61.48%
Thyroid receptor binding - 0.6889 68.89%
Glucocorticoid receptor binding - 0.6722 67.22%
Aromatase binding - 0.8377 83.77%
PPAR gamma - 0.7995 79.95%
Honey bee toxicity - 0.8917 89.17%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.8000 80.00%
Fish aquatic toxicity + 0.9922 99.22%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.40% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.17% 95.56%
CHEMBL3359 P21462 Formyl peptide receptor 1 87.69% 93.56%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 86.43% 97.21%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.71% 90.71%
CHEMBL2581 P07339 Cathepsin D 82.48% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.33% 97.25%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 12896705
LOTUS LTS0197662
wikiData Q104978386