CX-659S
Basic information
- CAS
204980-81-4- Standard SMILES
Cc1c(C)c2c(c(C)c1O)CC[C@@](C)(C(=O)Nc1c(N)n(-c3ccccc3)c(=O)n(C)c1=O)O2- InChIKey
NOYZWUQUALADDO-VWLOTQADSA-N- Molecular formula
- C25H28N4O5
- Average molar mass
- 464.5 g/mol
- Monoisotopic mass
- 464.20597001
Overview
structure in first source
Names & identifiers
- Preferred name
- CX-659S
- IUPAC
- (2S)-N-(4-amino-1-methyl-2,6-dioxo-3-phenylpyrimidin-5-yl)-6-hydroxy-2,5,7,8-tetramethyl-3,4-dihydrochromene-2-carboxamide
- English name
- 2H-1-Benzopyran-2-carboxamide, N-(6-amino-1,2,3,4-tetrahydro-3-methyl-2,4-dioxo-1-phenyl-5-pyrimidinyl)-3,4-dihydro-6-hydroxy-2,5,7,8-tetramethyl-, (2S)-
- Molecular formula
- C25H28N4O5
- Molecular weight
- 464.51
Names & synonyms
CX-659S204980-81-4YG2F04AVMQ2H-1-Benzopyran-2-carboxamide, N-(6-amino-1,2,3,4-tetrahydro-3-methyl-2,4-dioxo-1-phenyl-5-pyrimidinyl)-3,4-dihydro-6-hydroxy-2,5,7,8-tetramethyl-, (2S)-(-)-Cx-659SCX 659S2H-1-Benzopyran-2-carboxamide, N-(6-amino-1,2,3,4-tetrahydro-3-methyl-2,4-dioxo-1-phenyl-5-pyrimidinyl)-3,4-dihydro-6-hydroxy-2,5,7,8-tetramethyl-, (S)-RefChem:200284UNII-YG2F04AVMQ(2S)-N-(4-amino-1-methyl-2,6-dioxo-3-phenylpyrimidin-5-yl)-6-hydroxy-2,5,7,8-tetramethyl-3,4-dihydrochromene-2-carboxamideorb1697635CHEMBL3764203
Show more names
SCHEMBL29403469GLXC-07635AKOS040751342T31126Q27294504
Database identifiers
- CAS
204980-81-4- PubChem CID
Properties
Computed structural properties
- XLogP
- 2.9
- Topological polar surface area
- 125 Ų
- Hydrogen bond donors
- 3
- Hydrogen bond acceptors
- 6
- Rotatable bonds
- 3
- Heavy atoms
- 34
- Formal charge
- 0
- Complexity
- 885
Physicochemical properties
- FDA UNII
- 2 F04AVMQ · YG2F04AVMQ
Chemistry & industry
Pharmacology
MeSH Pharmacological Classification
Anti-inflammatory agents that are non-steroidal in nature. In addition to anti-inflammatory actions, they have analgesic, antipyretic, and platelet-inhibitory actions. They act by blocking the synthesis of prostaglandins by inhibiting cyclooxygenase, which converts arachidonic acid to cyclic endoperoxides, precursors of prostaglandins. Inhibition of prostaglandin synthesis accounts for their analgesic, antipyretic, and platelet-inhibitory actions; other mechanisms may contribute to their anti-inflammatory effects.
Drugs used to treat or prevent skin disorders or for the routine care of skin.
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Compound notes
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