4a-hydroxy-5-methyl-8-propan-2-yl-4,5,6,7,8,8a-hexahydro-3H-naphthalene-2-carboxylic acid

Details

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Internal ID 991f120d-ed2c-4001-ab56-4a190c597e75
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 4a-hydroxy-5-methyl-8-propan-2-yl-4,5,6,7,8,8a-hexahydro-3H-naphthalene-2-carboxylic acid
SMILES (Canonical) CC1CCC(C2C1(CCC(=C2)C(=O)O)O)C(C)C
SMILES (Isomeric) CC1CCC(C2C1(CCC(=C2)C(=O)O)O)C(C)C
InChI InChI=1S/C15H24O3/c1-9(2)12-5-4-10(3)15(18)7-6-11(14(16)17)8-13(12)15/h8-10,12-13,18H,4-7H2,1-3H3,(H,16,17)
InChI Key ISNQOHCTTZIKKK-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 3.00
Atomic LogP (AlogP) 2.84
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 4a-hydroxy-5-methyl-8-propan-2-yl-4,5,6,7,8,8a-hexahydro-3H-naphthalene-2-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 + 0.9968 99.68%
Caco-2 + 0.8670 86.70%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.8518 85.18%
OATP2B1 inhibitior - 0.8515 85.15%
OATP1B1 inhibitior + 0.9365 93.65%
OATP1B3 inhibitior + 0.9208 92.08%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior + 0.5250 52.50%
BSEP inhibitior - 0.9432 94.32%
P-glycoprotein inhibitior - 0.9561 95.61%
P-glycoprotein substrate - 0.8545 85.45%
CYP3A4 substrate - 0.5177 51.77%
CYP2C9 substrate - 0.7859 78.59%
CYP2D6 substrate - 0.9169 91.69%
CYP3A4 inhibition - 0.8108 81.08%
CYP2C9 inhibition - 0.9137 91.37%
CYP2C19 inhibition - 0.9019 90.19%
CYP2D6 inhibition - 0.9527 95.27%
CYP1A2 inhibition - 0.9223 92.23%
CYP2C8 inhibition - 0.9536 95.36%
CYP inhibitory promiscuity - 0.9047 90.47%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6007 60.07%
Eye corrosion - 0.9954 99.54%
Eye irritation - 0.7545 75.45%
Skin irritation + 0.6455 64.55%
Skin corrosion - 0.9678 96.78%
Ames mutagenesis - 0.8170 81.70%
Human Ether-a-go-go-Related Gene inhibition - 0.7506 75.06%
Micronuclear - 0.8800 88.00%
Hepatotoxicity + 0.5166 51.66%
skin sensitisation + 0.6431 64.31%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity - 0.8146 81.46%
Acute Oral Toxicity (c) III 0.7946 79.46%
Estrogen receptor binding - 0.5793 57.93%
Androgen receptor binding - 0.5191 51.91%
Thyroid receptor binding + 0.5505 55.05%
Glucocorticoid receptor binding + 0.6849 68.49%
Aromatase binding - 0.6395 63.95%
PPAR gamma - 0.7913 79.13%
Honey bee toxicity - 0.9374 93.74%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity + 0.9951 99.51%

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 96.17% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.67% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.05% 95.56%
CHEMBL2581 P07339 Cathepsin D 86.48% 98.95%
CHEMBL4227 P25090 Lipoxin A4 receptor 84.64% 100.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.00% 93.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.72% 99.23%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.69% 100.00%
CHEMBL5028 O14672 ADAM10 80.63% 97.50%

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 163024906
LOTUS LTS0092404
wikiData Q104169084