Isoquinoline

Details

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Internal ID b90ad85f-e5cd-4087-99de-a7268ca12eb6
Taxonomy Organoheterocyclic compounds > Isoquinolines and derivatives
IUPAC Name isoquinoline
SMILES (Canonical) C1=CC=C2C=NC=CC2=C1
SMILES (Isomeric) C1=CC=C2C=NC=CC2=C1
InChI InChI=1S/C9H7N/c1-2-4-9-7-10-6-5-8(9)3-1/h1-7H
InChI Key AWJUIBRHMBBTKR-UHFFFAOYSA-N
Popularity 6,156 references in papers

Physical and Chemical Properties

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Molecular Formula C9H7N
Molecular Weight 129.16 g/mol
Exact Mass 129.057849228 g/mol
Topological Polar Surface Area (TPSA) 12.90 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.23
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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119-65-3
2-Benzazine
2-Azanaphthalene
Leucoline
Isochinolin
beta-Quinoline
Benzo[c]pyridine
Benzo(c)pyridine
3,4-Benzopyridine
FEMA No. 2978
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Isoquinoline

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9937 99.37%
Caco-2 + 0.9669 96.69%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Lysosomes 0.6283 62.83%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9747 97.47%
OATP1B3 inhibitior + 0.9692 96.92%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8164 81.64%
P-glycoprotein inhibitior - 0.9858 98.58%
P-glycoprotein substrate - 0.9887 98.87%
CYP3A4 substrate - 0.8193 81.93%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7110 71.10%
CYP3A4 inhibition - 0.5818 58.18%
CYP2C9 inhibition + 0.6012 60.12%
CYP2C19 inhibition + 0.8223 82.23%
CYP2D6 inhibition - 0.5080 50.80%
CYP1A2 inhibition + 0.9283 92.83%
CYP2C8 inhibition + 0.5961 59.61%
CYP inhibitory promiscuity + 0.5718 57.18%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7600 76.00%
Carcinogenicity (trinary) Non-required 0.5977 59.77%
Eye corrosion - 0.7278 72.78%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.9275 92.75%
Skin corrosion - 0.8849 88.49%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6954 69.54%
Micronuclear - 0.6142 61.42%
Hepatotoxicity + 0.8532 85.32%
skin sensitisation + 0.6526 65.26%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity - 0.6222 62.22%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity + 0.5642 56.42%
Acute Oral Toxicity (c) II 0.7518 75.18%
Estrogen receptor binding - 0.7347 73.47%
Androgen receptor binding - 0.8522 85.22%
Thyroid receptor binding - 0.7783 77.83%
Glucocorticoid receptor binding - 0.8215 82.15%
Aromatase binding - 0.6603 66.03%
PPAR gamma - 0.8450 84.50%
Honey bee toxicity - 0.9358 93.58%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.8100 81.00%
Fish aquatic toxicity - 0.4946 49.46%

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
CHEMBL308 P06493 Cyclin-dependent kinase 1 87.53% 91.73%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 86.10% 85.30%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 85.33% 94.62%
CHEMBL221 P23219 Cyclooxygenase-1 82.51% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.55% 86.33%
CHEMBL3902 P09211 Glutathione S-transferase Pi 80.21% 93.81%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Lonicera japonica

Cross-Links

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PubChem 8405
NPASS NPC143603
LOTUS LTS0089583
wikiData Q412316