4,9,9-Trimethyl-2,4,5,6,7,8-hexahydro-3h-3a,7-methanoazulene-1-carboxylic acid

Details

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Internal ID db51409a-b02d-473d-85c8-0d6e004f460a
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 10,11,11-trimethyltricyclo[5.3.1.01,5]undec-4-ene-4-carboxylic acid
SMILES (Canonical) CC1CCC2CC3=C(CCC13C2(C)C)C(=O)O
SMILES (Isomeric) CC1CCC2CC3=C(CCC13C2(C)C)C(=O)O
InChI InChI=1S/C15H22O2/c1-9-4-5-10-8-12-11(13(16)17)6-7-15(9,12)14(10,2)3/h9-10H,4-8H2,1-3H3,(H,16,17)
InChI Key MFODEBYPUFXURM-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 3.60
Atomic LogP (AlogP) 3.62
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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DTXSID70920867

2D Structure

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2D Structure of 4,9,9-Trimethyl-2,4,5,6,7,8-hexahydro-3h-3a,7-methanoazulene-1-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 + 0.9962 99.62%
Caco-2 + 0.8835 88.35%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.4700 47.00%
OATP2B1 inhibitior - 0.8480 84.80%
OATP1B1 inhibitior + 0.8743 87.43%
OATP1B3 inhibitior - 0.3270 32.70%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior - 0.8955 89.55%
P-glycoprotein inhibitior - 0.9368 93.68%
P-glycoprotein substrate - 0.8777 87.77%
CYP3A4 substrate + 0.5185 51.85%
CYP2C9 substrate - 0.7907 79.07%
CYP2D6 substrate - 0.9038 90.38%
CYP3A4 inhibition - 0.9379 93.79%
CYP2C9 inhibition + 0.7176 71.76%
CYP2C19 inhibition + 0.6246 62.46%
CYP2D6 inhibition - 0.9247 92.47%
CYP1A2 inhibition - 0.7080 70.80%
CYP2C8 inhibition - 0.8523 85.23%
CYP inhibitory promiscuity - 0.8831 88.31%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.5959 59.59%
Eye corrosion - 0.9705 97.05%
Eye irritation + 0.7522 75.22%
Skin irritation - 0.5229 52.29%
Skin corrosion - 0.9776 97.76%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6547 65.47%
Micronuclear - 0.9400 94.00%
Hepatotoxicity - 0.5248 52.48%
skin sensitisation + 0.7244 72.44%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.5111 51.11%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity + 0.5289 52.89%
Acute Oral Toxicity (c) III 0.6532 65.32%
Estrogen receptor binding - 0.6439 64.39%
Androgen receptor binding - 0.5446 54.46%
Thyroid receptor binding - 0.6431 64.31%
Glucocorticoid receptor binding - 0.5877 58.77%
Aromatase binding - 0.7997 79.97%
PPAR gamma - 0.5776 57.76%
Honey bee toxicity - 0.9334 93.34%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6500 65.00%
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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.00% 96.09%
CHEMBL233 P35372 Mu opioid receptor 86.59% 97.93%
CHEMBL217 P14416 Dopamine D2 receptor 86.58% 95.62%
CHEMBL221 P23219 Cyclooxygenase-1 85.45% 90.17%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 83.61% 93.00%
CHEMBL340 P08684 Cytochrome P450 3A4 82.75% 91.19%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.80% 93.04%
CHEMBL2581 P07339 Cathepsin D 80.06% 98.95%

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.
Cyperus rotundus
Joannesia princeps

Cross-Links

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PubChem 188673
LOTUS LTS0166341
wikiData Q82893584