7-(2-Hydroxypropan-2-yl)-1-methyl-1,2,3,5,6,7,8,8a-octahydroazulene-4-carboxylic acid

Details

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Internal ID 449c6b31-47c4-4d82-8167-b0f966af99fa
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 7-(2-hydroxypropan-2-yl)-1-methyl-1,2,3,5,6,7,8,8a-octahydroazulene-4-carboxylic acid
SMILES (Canonical) CC1CCC2=C(CCC(CC12)C(C)(C)O)C(=O)O
SMILES (Isomeric) CC1CCC2=C(CCC(CC12)C(C)(C)O)C(=O)O
InChI InChI=1S/C15H24O3/c1-9-4-6-11-12(14(16)17)7-5-10(8-13(9)11)15(2,3)18/h9-10,13,18H,4-8H2,1-3H3,(H,16,17)
InChI Key GNHYOXJPHJUUIT-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O3
Molecular Weight 252.35 g/mol
Exact Mass 252.17254462 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.98
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-(2-Hydroxypropan-2-yl)-1-methyl-1,2,3,5,6,7,8,8a-octahydroazulene-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 + 0.9926 99.26%
Caco-2 + 0.7337 73.37%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.6559 65.59%
OATP2B1 inhibitior - 0.8474 84.74%
OATP1B1 inhibitior + 0.9288 92.88%
OATP1B3 inhibitior + 0.8606 86.06%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior - 0.9079 90.79%
P-glycoprotein inhibitior - 0.9255 92.55%
P-glycoprotein substrate - 0.8737 87.37%
CYP3A4 substrate - 0.5176 51.76%
CYP2C9 substrate - 0.7859 78.59%
CYP2D6 substrate - 0.9169 91.69%
CYP3A4 inhibition - 0.9197 91.97%
CYP2C9 inhibition + 0.5322 53.22%
CYP2C19 inhibition - 0.6673 66.73%
CYP2D6 inhibition - 0.9214 92.14%
CYP1A2 inhibition - 0.5708 57.08%
CYP2C8 inhibition - 0.7146 71.46%
CYP inhibitory promiscuity - 0.8328 83.28%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8200 82.00%
Carcinogenicity (trinary) Non-required 0.5894 58.94%
Eye corrosion - 0.9717 97.17%
Eye irritation + 0.5317 53.17%
Skin irritation - 0.5307 53.07%
Skin corrosion - 0.9702 97.02%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6254 62.54%
Micronuclear - 0.8800 88.00%
Hepatotoxicity + 0.5836 58.36%
skin sensitisation + 0.6501 65.01%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.7279 72.79%
Acute Oral Toxicity (c) III 0.6342 63.42%
Estrogen receptor binding - 0.6530 65.30%
Androgen receptor binding - 0.5606 56.06%
Thyroid receptor binding + 0.6556 65.56%
Glucocorticoid receptor binding + 0.5844 58.44%
Aromatase binding - 0.8628 86.28%
PPAR gamma - 0.5055 50.55%
Honey bee toxicity - 0.9548 95.48%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity + 0.9945 99.45%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.94% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.24% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.11% 95.56%
CHEMBL3359 P21462 Formyl peptide receptor 1 85.45% 93.56%
CHEMBL2581 P07339 Cathepsin D 85.18% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.00% 97.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.47% 99.23%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 82.03% 93.00%
CHEMBL340 P08684 Cytochrome P450 3A4 81.95% 91.19%

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 162979245
LOTUS LTS0262155
wikiData Q105012542