Pyrido(2,3-d)pyrimidine

Details

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Internal ID 90737ece-fba5-4ebb-b562-8b82aa934424
Taxonomy Organoheterocyclic compounds > Pyridopyrimidines > Pyrido[2,3-d]pyrimidines
IUPAC Name pyrido[2,3-d]pyrimidine
SMILES (Canonical) C1=CC2=CN=CN=C2N=C1
SMILES (Isomeric) C1=CC2=CN=CN=C2N=C1
InChI InChI=1S/C7H5N3/c1-2-6-4-8-5-10-7(6)9-3-1/h1-5H
InChI Key UDJFFSGCRRMVFH-UHFFFAOYSA-N
Popularity 286 references in papers

Physical and Chemical Properties

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Molecular Formula C7H5N3
Molecular Weight 131.13 g/mol
Exact Mass 131.048347172 g/mol
Topological Polar Surface Area (TPSA) 38.70 Ų
XlogP 0.80
Atomic LogP (AlogP) 1.02
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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254-61-5
1,3,8-Triazanaphthalene
pyrido[2
Pyrido[2,3-d]pyrimidin
pyrido[2,3-d]-pyrimidine
SCHEMBL12414
DTXSID90342547

2D Structure

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2D Structure of Pyrido(2,3-d)pyrimidine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9961 99.61%
Caco-2 + 0.8624 86.24%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7857 78.57%
Subcellular localzation Mitochondria 0.4420 44.20%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9758 97.58%
OATP1B3 inhibitior + 0.9602 96.02%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior - 0.8775 87.75%
P-glycoprotein inhibitior - 0.9897 98.97%
P-glycoprotein substrate - 0.9691 96.91%
CYP3A4 substrate - 0.7342 73.42%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7110 71.10%
CYP3A4 inhibition - 0.8135 81.35%
CYP2C9 inhibition - 0.8758 87.58%
CYP2C19 inhibition - 0.9391 93.91%
CYP2D6 inhibition - 0.9800 98.00%
CYP1A2 inhibition + 0.9217 92.17%
CYP2C8 inhibition - 0.7674 76.74%
CYP inhibitory promiscuity - 0.7042 70.42%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.7314 73.14%
Eye corrosion - 0.9485 94.85%
Eye irritation + 0.9942 99.42%
Skin irritation + 0.6457 64.57%
Skin corrosion - 0.9228 92.28%
Ames mutagenesis + 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6879 68.79%
Micronuclear + 0.6059 60.59%
Hepatotoxicity + 0.7875 78.75%
skin sensitisation - 0.7860 78.60%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity + 0.6807 68.07%
Acute Oral Toxicity (c) III 0.7991 79.91%
Estrogen receptor binding - 0.7351 73.51%
Androgen receptor binding - 0.8162 81.62%
Thyroid receptor binding - 0.6958 69.58%
Glucocorticoid receptor binding - 0.8656 86.56%
Aromatase binding - 0.5236 52.36%
PPAR gamma - 0.7976 79.76%
Honey bee toxicity - 0.9474 94.74%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity - 0.7060 70.60%

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
CHEMBL288 Q08499 Phosphodiesterase 4D 88.53% 97.50%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 87.64% 85.30%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 87.21% 93.10%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.96% 94.00%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 81.87% 100.00%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 81.72% 96.67%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.60% 86.33%
CHEMBL2535 P11166 Glucose transporter 81.24% 98.75%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 81.13% 94.62%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.41% 96.09%
CHEMBL2243 O00519 Anandamide amidohydrolase 80.25% 97.53%

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.
Pinellia ternata

Cross-Links

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PubChem 582898
NPASS NPC246294