4,4a-dimethyl-5-prop-1-en-2-yl-2,3,4,5-tetrahydro-1H-naphthalene

Details

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Internal ID 3fc1dd69-e28e-4419-b1f6-f355c140ff62
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name 4,4a-dimethyl-5-prop-1-en-2-yl-2,3,4,5-tetrahydro-1H-naphthalene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H22/c1-11(2)14-10-6-9-13-8-5-7-12(3)15(13,14)4/h6,9-10,12,14H,1,5,7-8H2,2-4H3
InChI Key NDOOUZVSWOMXFH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22
Molecular Weight 202.33 g/mol
Exact Mass 202.172150702 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.20
Atomic LogP (AlogP) 4.50
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4,4a-dimethyl-5-prop-1-en-2-yl-2,3,4,5-tetrahydro-1H-naphthalene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9938 99.38%
Caco-2 + 0.8975 89.75%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Lysosomes 0.7755 77.55%
OATP2B1 inhibitior - 0.8575 85.75%
OATP1B1 inhibitior + 0.8888 88.88%
OATP1B3 inhibitior + 0.8007 80.07%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.9331 93.31%
P-glycoprotein inhibitior - 0.9600 96.00%
P-glycoprotein substrate - 0.8265 82.65%
CYP3A4 substrate + 0.5278 52.78%
CYP2C9 substrate - 0.6219 62.19%
CYP2D6 substrate - 0.7767 77.67%
CYP3A4 inhibition - 0.8384 83.84%
CYP2C9 inhibition - 0.7526 75.26%
CYP2C19 inhibition - 0.6357 63.57%
CYP2D6 inhibition - 0.9200 92.00%
CYP1A2 inhibition - 0.7933 79.33%
CYP2C8 inhibition - 0.6963 69.63%
CYP inhibitory promiscuity - 0.5590 55.90%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Non-required 0.4644 46.44%
Eye corrosion - 0.9565 95.65%
Eye irritation - 0.8377 83.77%
Skin irritation - 0.6095 60.95%
Skin corrosion - 0.9493 94.93%
Ames mutagenesis - 0.6354 63.54%
Human Ether-a-go-go-Related Gene inhibition + 0.7529 75.29%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation + 0.7949 79.49%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity + 0.5111 51.11%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity - 0.6946 69.46%
Acute Oral Toxicity (c) III 0.7863 78.63%
Estrogen receptor binding - 0.8868 88.68%
Androgen receptor binding - 0.6816 68.16%
Thyroid receptor binding - 0.6908 69.08%
Glucocorticoid receptor binding - 0.8828 88.28%
Aromatase binding - 0.7154 71.54%
PPAR gamma - 0.7922 79.22%
Honey bee toxicity - 0.8906 89.06%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5900 59.00%
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 95.89% 96.09%
CHEMBL1951 P21397 Monoamine oxidase A 95.72% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.30% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.71% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.20% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.05% 100.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.33% 92.94%
CHEMBL2581 P07339 Cathepsin D 82.78% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.87% 86.33%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.08% 93.04%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.06% 95.89%

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 154287462
LOTUS LTS0032111
wikiData Q104172362