Weight | 119.127 g/mol |
---|---|
Formula | C6H5N3 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 1 |
Aromatic Rings | 2 |
Rotatable Bonds | 0 |
7H-Pyrrolo[2,3-d]pyrimidine (271-70-5)
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- Inhibition of Ca2+-pump ATPase and the Na+/K+-pump ATPase by iron-generated free radicals: Protection by 6,7-dimethyl-2,4-di-1-pyrrolidinyl-7h-pyrrolo[2,3-d]pyrimidine sulfate (U-89843D), a potent, novel, antioxidant/free radical scavenger (Biochemical Pharmacology, 1996)
- Novel 7H-pyrrolo[2,3-d]pyrimidine derivatives as potent and orally active STAT6 inhibitors. (Bioorganic & Medicinal Chemistry, 2009)
- Synthesis of pyrazolo[3,4-d]pyrimidine analogues of the potent antitumor agent N-{4-[2-(2-amino-4(3H)-oxo-7H-pyrrolo[2,3-d]pyrimidin-5-yl)ethyl]benzoyl}-L-glutamic acid (LY231514) (Heterocycles, 1996)
- Synthesis and in vitro EGFR (ErbB1) tyrosine kinase inhibitory activity of 4-N-substituted 6-aryl-7H-pyrrolo[2,3-d]pyrimidine-4-amines (European Journal of Medicinal Chemistry, 2011)
- Synthesis and Biological Activity of N4-phenylsubstituted-6-(2,4-dichloro phenylmethyl)-7H-pyrrolo[2,3-d]pyrimidine-2,4-diamines as Vascular Endothelial Growth Factor Receptor-2 Inhibitors and Antiangiogenic and Antitumor Agents (Bioorganic & Medicinal Chemistry, 2010)
- Synthetic Studies of Potential Antimetabolites. X.1Synthesis of 4-Hydroxy-7--D-ribofuranosyl-7H-pyrrolo[2,3-d]pyrimidine, a Tubercidin Analog (Journal of Organic Chemistry, 1963)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CNC2=NC=NC=C21
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InChIKeyJJTNLWSCFYERCK-UHFFFAOYSA-N
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Similar Compounds
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