5aTHQ-10n

Details

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Internal ID 5f35d33c-e15b-4988-8415-039bd192152e
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Hydroquinolines
IUPAC Name 5-decyl-1,2,3,4-tetrahydroquinoline
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H31N/c1-2-3-4-5-6-7-8-9-12-17-13-10-15-19-18(17)14-11-16-20-19/h10,13,15,20H,2-9,11-12,14,16H2,1H3
InChI Key KGRXIUJPGZFPLO-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C19H31N
Molecular Weight 273.50 g/mol
Exact Mass 273.245649993 g/mol
Topological Polar Surface Area (TPSA) 12.00 Ų
XlogP 7.40
Atomic LogP (AlogP) 5.73
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5aTHQ-10n

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9971 99.71%
Caco-2 + 0.8693 86.93%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Lysosomes 0.7489 74.89%
OATP2B1 inhibitior - 0.8576 85.76%
OATP1B1 inhibitior + 0.9607 96.07%
OATP1B3 inhibitior + 0.9459 94.59%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior + 0.7250 72.50%
BSEP inhibitior - 0.5554 55.54%
P-glycoprotein inhibitior - 0.7050 70.50%
P-glycoprotein substrate - 0.5411 54.11%
CYP3A4 substrate - 0.5238 52.38%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate + 0.6457 64.57%
CYP3A4 inhibition + 0.6267 62.67%
CYP2C9 inhibition - 0.8619 86.19%
CYP2C19 inhibition - 0.6259 62.59%
CYP2D6 inhibition + 0.7998 79.98%
CYP1A2 inhibition + 0.8757 87.57%
CYP2C8 inhibition - 0.7559 75.59%
CYP inhibitory promiscuity - 0.6469 64.69%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.8182 81.82%
Eye corrosion - 0.9527 95.27%
Eye irritation - 0.5179 51.79%
Skin irritation - 0.5958 59.58%
Skin corrosion - 0.6778 67.78%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8566 85.66%
Micronuclear - 0.6900 69.00%
Hepatotoxicity - 0.5349 53.49%
skin sensitisation - 0.7838 78.38%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity - 0.7217 72.17%
Acute Oral Toxicity (c) III 0.6552 65.52%
Estrogen receptor binding + 0.5853 58.53%
Androgen receptor binding + 0.5389 53.89%
Thyroid receptor binding + 0.7680 76.80%
Glucocorticoid receptor binding - 0.8001 80.01%
Aromatase binding - 0.6535 65.35%
PPAR gamma + 0.7333 73.33%
Honey bee toxicity - 0.9856 98.56%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.6258 62.58%
Fish aquatic toxicity + 0.9511 95.11%

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
CHEMBL2581 P07339 Cathepsin D 98.83% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 97.71% 89.63%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.79% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.34% 96.09%
CHEMBL5805 Q9NR97 Toll-like receptor 8 93.00% 96.25%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 92.68% 92.08%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.42% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.13% 97.09%
CHEMBL3192 Q9BY41 Histone deacetylase 8 91.39% 93.99%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.86% 86.33%
CHEMBL2996 Q05655 Protein kinase C delta 89.04% 97.79%
CHEMBL1907 P15144 Aminopeptidase N 88.94% 93.31%
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 88.18% 96.42%
CHEMBL1907598 P05106 Integrin alpha-V/beta-3 86.39% 95.71%
CHEMBL3401 O75469 Pregnane X receptor 85.38% 94.73%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 84.46% 91.81%
CHEMBL228 P31645 Serotonin transporter 82.53% 95.51%
CHEMBL3310 Q96DB2 Histone deacetylase 11 81.44% 88.56%
CHEMBL255 P29275 Adenosine A2b receptor 80.94% 98.59%
CHEMBL2535 P11166 Glucose transporter 80.61% 98.75%

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 106778710
LOTUS LTS0071288
wikiData Q75058917