CHEBI:91460 - KN-93

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name KN-93
ChEBI ID CHEBI:91460
Definition A sulfonamide resulting from the formal condensation of p-methoxybenzenesulfonic acid with the anilino nitrogen of 2-(aminomethyl)-N-(2-hydroxyethyl)aniline in which the hydrogens of the primary amino group have been replaced by methyl and p-chlorocinnamyl groups. KN-93 is a selective inhibitor of Ca2+/calmodulin-dependent protein kinase II.
Stars This entity has been manually annotated by the ChEBI Team.
Download Molfile XML SDF
Formula C26H29ClN2O4S
Net Charge 0
Average Mass 501.039
Monoisotopic Mass 500.15366
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Biological Role(s): EC 2.7.11.17 (Ca(2+)/calmodulin-dependent protein kinase) inhibitor
Any EC 2.7.11.* (protein-serine/threonine kinase) inhibitor that interferes with the action of a Ca2+/calmodulin-dependent protein kinase (EC 2.7.11.17).
Application(s): geroprotector
Any compound that supports healthy aging, slows the biological aging process, or extends lifespan.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing KN-93 (CHEBI:91460) has role EC 2.7.11.17 (Ca2+/calmodulin-dependent protein kinase) inhibitor (CHEBI:131794)
KN-93 (CHEBI:91460) has role geroprotector (CHEBI:176497)
KN-93 (CHEBI:91460) is a monochlorobenzenes (CHEBI:83403)
KN-93 (CHEBI:91460) is a monomethoxybenzene (CHEBI:25235)
KN-93 (CHEBI:91460) is a primary alcohol (CHEBI:15734)
KN-93 (CHEBI:91460) is a sulfonamide (CHEBI:35358)
KN-93 (CHEBI:91460) is a tertiary amino compound (CHEBI:50996)
IUPAC Name
N-[2-({[(2E)-3-(4-chlorophenyl)prop-2-en-1-yl](methyl)amino}methyl)phenyl]-N-(2-hydroxyethyl)-4-methoxybenzenesulfonamide
Synonyms Sources
KN 93 ChemIDplus
KN93 ChEBI
N-[2-[[3-(4-chlorophenyl)prop-2-enyl-methylamino]methyl]phenyl]-N-(2-hydroxyethyl)-4-methoxybenzenesulfonamide LINCS
Manual Xref Database
LSM-42804 LINCS
View more database links
Registry Numbers Types Sources
139298-40-1 CAS Registry Number ChemIDplus
8359108 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
10712242 PubMed citation Europe PMC
16368898 PubMed citation Europe PMC
1662507 PubMed citation Europe PMC
17457979 PubMed citation Europe PMC
22363408 PubMed citation Europe PMC
23983471 PubMed citation Europe PMC
24142712 PubMed citation Europe PMC
24829059 PubMed citation Europe PMC
24836181 PubMed citation Europe PMC
25206480 PubMed citation Europe PMC
25498987 PubMed citation Europe PMC
25937575 PubMed citation Europe PMC
26024774 PubMed citation Europe PMC
26463508 PubMed citation Europe PMC
9864285 PubMed citation Europe PMC
Last Modified
26 October 2021