(1S,7aR)-1,5,5,7a-tetramethyl-2,3,6,7-tetrahydro-1H-indene-4-carboxylic acid

Details

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Internal ID ced95eb4-0b71-4763-9d96-d9eb2b86b0da
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Carboxylic acids
IUPAC Name (1S,7aR)-1,5,5,7a-tetramethyl-2,3,6,7-tetrahydro-1H-indene-4-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H22O2/c1-9-5-6-10-11(12(15)16)13(2,3)7-8-14(9,10)4/h9H,5-8H2,1-4H3,(H,15,16)/t9-,14+/m0/s1
InChI Key PHGGTDBZXHQBFS-LKFCYVNXSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C14H22O2
Molecular Weight 222.32 g/mol
Exact Mass 222.161979940 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 3.80
Atomic LogP (AlogP) 3.62
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1S,7aR)-1,5,5,7a-tetramethyl-2,3,6,7-tetrahydro-1H-indene-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 + 0.9954 99.54%
Caco-2 + 0.8692 86.92%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.4564 45.64%
OATP2B1 inhibitior - 0.8411 84.11%
OATP1B1 inhibitior + 0.9203 92.03%
OATP1B3 inhibitior - 0.2658 26.58%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior + 0.5250 52.50%
BSEP inhibitior - 0.8764 87.64%
P-glycoprotein inhibitior - 0.9328 93.28%
P-glycoprotein substrate - 0.9537 95.37%
CYP3A4 substrate - 0.5260 52.60%
CYP2C9 substrate - 0.7829 78.29%
CYP2D6 substrate - 0.9180 91.80%
CYP3A4 inhibition - 0.9217 92.17%
CYP2C9 inhibition - 0.6448 64.48%
CYP2C19 inhibition - 0.5721 57.21%
CYP2D6 inhibition - 0.9337 93.37%
CYP1A2 inhibition - 0.6999 69.99%
CYP2C8 inhibition - 0.9000 90.00%
CYP inhibitory promiscuity - 0.8253 82.53%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.6106 61.06%
Eye corrosion - 0.9859 98.59%
Eye irritation + 0.8488 84.88%
Skin irritation + 0.6155 61.55%
Skin corrosion - 0.9797 97.97%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.9400 94.00%
Hepatotoxicity + 0.5105 51.05%
skin sensitisation + 0.7510 75.10%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.6302 63.02%
Acute Oral Toxicity (c) III 0.7205 72.05%
Estrogen receptor binding - 0.9061 90.61%
Androgen receptor binding - 0.8184 81.84%
Thyroid receptor binding - 0.5738 57.38%
Glucocorticoid receptor binding - 0.7957 79.57%
Aromatase binding - 0.7889 78.89%
PPAR gamma - 0.8238 82.38%
Honey bee toxicity - 0.9470 94.70%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.7200 72.00%
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 95.96% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 87.40% 90.17%
CHEMBL2581 P07339 Cathepsin D 86.03% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.64% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.91% 95.56%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 83.48% 93.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.25% 91.11%
CHEMBL340 P08684 Cytochrome P450 3A4 82.18% 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 163156470
LOTUS LTS0164877
wikiData Q105208945