N-tosyl-L-phenylalanyl chloromethyl ketone
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N-tosyl-L-phenylalanyl chloromethyl ketone
Summary
N-tosyl-L-phenylalanyl chloromethyl ketone is a type of chemical entity[1]. It ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (23 views/month).[2]
Key Facts
- N-tosyl-L-phenylalanyl chloromethyl ketone's instance of is recorded as type of chemical entity[3].
- N-tosyl-L-phenylalanyl chloromethyl ketone's canonical SMILES is recorded as CC1=CC=C(C=C1)S(=O)(=O)NC(CC2=CC=CC=C2)C(=O)CCl[4].
- N-tosyl-L-phenylalanyl chloromethyl ketone's chemical formula is recorded as C₁₇H₁₈ClNO₃S[5].
- N-tosyl-L-phenylalanyl chloromethyl ketone is a type of N-(4-Chloro-3-oxo-1-phenylbutan-2-yl)-4-methylbenzene-1-sulfonamide[6].
- N-tosyl-L-phenylalanyl chloromethyl ketone's found in taxon is recorded as Chaetomium globosum[7].
- N-tosyl-L-phenylalanyl chloromethyl ketone's found in taxon is recorded as Spongia[8].
- N-tosyl-L-phenylalanyl chloromethyl ketone's found in taxon is recorded as Streptomyces[9].
- N-tosyl-L-phenylalanyl chloromethyl ketone's found in taxon is recorded as Aspergillus terreus[10].
- N-tosyl-L-phenylalanyl chloromethyl ketone's isomeric SMILES is recorded as CC1=CC=C(C=C1)S(=O)(=O)NC@@HC(=O)CClC@@HC(=O)CCl">[11].
- N-tosyl-L-phenylalanyl chloromethyl ketone's mass is recorded as {'unit': 'Q483261', 'amount': '+351.07'}[12].
- N-tosyl-L-phenylalanyl chloromethyl ketone's subject has role is recorded as alkylating agent[13].
- N-tosyl-L-phenylalanyl chloromethyl ketone's subject has role is recorded as protein synthesis inhibitor[14].
- N-tosyl-L-phenylalanyl chloromethyl ketone's subject has role is recorded as serine proteinase inhibitor[15].
- N-tosyl-L-phenylalanyl chloromethyl ketone's stereoisomer of is recorded as N-[(2R)-4-chloro-3-oxo-1-phenylbutan-2-yl]-4-methylbenzenesulfonamide[16].
Why It Matters
N-tosyl-L-phenylalanyl chloromethyl ketone ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (23 views/month).[2] It is known by 6 alternative names across languages and contexts.[17]