Dihydropyridine

Details

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Internal ID 117c6338-560b-424c-b784-cce12605aafc
Taxonomy Organoheterocyclic compounds > Pyridines and derivatives > Hydropyridines > Dihydropyridines
IUPAC Name 1,2-dihydropyridine
SMILES (Canonical) C1C=CC=CN1
SMILES (Isomeric) C1C=CC=CN1
InChI InChI=1S/C5H7N/c1-2-4-6-5-3-1/h1-4,6H,5H2
InChI Key MMWRGWQTAMNAFC-UHFFFAOYSA-N
Popularity 7,763 references in papers

Physical and Chemical Properties

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Molecular Formula C5H7N
Molecular Weight 81.12 g/mol
Exact Mass 81.057849228 g/mol
Topological Polar Surface Area (TPSA) 12.00 Ų
XlogP 1.10
Atomic LogP (AlogP) 0.66
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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Dihydropyridine
22694-45-7
Pyridine, 1,2-dihydro-
YA306KG67U
Dihydropyridines
dihydroazine
UNII-YA306KG67U
DTXSID80945364
MMWRGWQTAMNAFC-UHFFFAOYSA-N
AKOS006352484
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Dihydropyridine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9869 98.69%
Caco-2 + 0.8314 83.14%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Lysosomes 0.7096 70.96%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9654 96.54%
OATP1B3 inhibitior + 0.9573 95.73%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.9149 91.49%
P-glycoprotein inhibitior - 0.9870 98.70%
P-glycoprotein substrate - 0.9712 97.12%
CYP3A4 substrate - 0.7619 76.19%
CYP2C9 substrate + 0.6139 61.39%
CYP2D6 substrate - 0.7732 77.32%
CYP3A4 inhibition - 0.9160 91.60%
CYP2C9 inhibition - 0.7637 76.37%
CYP2C19 inhibition - 0.8358 83.58%
CYP2D6 inhibition - 0.7604 76.04%
CYP1A2 inhibition - 0.5337 53.37%
CYP2C8 inhibition - 0.9742 97.42%
CYP inhibitory promiscuity - 0.7157 71.57%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6900 69.00%
Carcinogenicity (trinary) Non-required 0.5663 56.63%
Eye corrosion + 0.9882 98.82%
Eye irritation + 0.9913 99.13%
Skin irritation + 0.8264 82.64%
Skin corrosion + 0.9239 92.39%
Ames mutagenesis - 0.5254 52.54%
Human Ether-a-go-go-Related Gene inhibition - 0.8027 80.27%
Micronuclear - 0.7600 76.00%
Hepatotoxicity + 0.7552 75.52%
skin sensitisation + 0.6490 64.90%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.7667 76.67%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity + 0.5439 54.39%
Acute Oral Toxicity (c) III 0.4892 48.92%
Estrogen receptor binding - 0.9310 93.10%
Androgen receptor binding - 0.8088 80.88%
Thyroid receptor binding - 0.8353 83.53%
Glucocorticoid receptor binding - 0.8230 82.30%
Aromatase binding - 0.8431 84.31%
PPAR gamma - 0.8482 84.82%
Honey bee toxicity - 0.7833 78.33%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity - 0.9037 90.37%

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
CHEMBL3310 Q96DB2 Histone deacetylase 11 81.72% 88.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.01% 94.45%
CHEMBL1937 Q92769 Histone deacetylase 2 80.66% 94.75%

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.
Nicotiana tabacum
Vitex negundo
Vitex negundo var. cannabifolia

Cross-Links

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PubChem 407038
LOTUS LTS0197541
wikiData Q105242714