(S,R,S)-AHPC-Me-C6-NH2

• CAT Number: I042655
• CAS Number: 2411422-49-4
• Molecular Formula: C30H45N5O4S
• Molecular Weight: 571.77
• Purity: ≥95%
• Synonyms: (2S,4R)-1-[(2S)-2-(7-aminoheptanoylamino)-3,3-dimethylbutanoyl]-4-hydroxy-N-[(1S)-1-[4-(4-methyl-1,3-thiazol-5-yl)phenyl]ethyl]pyrrolidine-2-carboxamide
• InChI: InChI=1S/C30H45N5O4S/c1-19(21-11-13-22(14-12-21)26-20(2)32-18-40-26)33-28(38)24-16-23(36)17-35(24)29(39)27(30(3,4)5)34-25(37)10-8-6-7-9-15-31/h11-14,18-19,23-24,27,36H,6-10,15-17,31H2,1-5H3,(H,33,38)(H,34,37)/t19-,23+,24-,27+/m0/s1
• InChIKey: UGZLQBJANUBKTH-BOALBMDWSA-N
• SMILES: CC1=C(SC=N1)C2=CC=C(C=C2)[C@H](C)NC(=O)[C@@H]3C[C@H](CN3C(=O)[C@H](C(C)(C)C)NC(=O)CCCCCCN)O

(S,R,S)-AHPC-Me-C6-NH2（Cat No.:I042655）is a chiral compound featuring a specific stereochemistry at the AHPC (aminohydroxypropylcyclohexane) core, along with a methyl group (Me) and an amino (NH2) group attached to a C6 benzene ring. This compound is used in synthetic chemistry and drug development, particularly in the design of bioactive molecules. Its structural features make it a valuable candidate for studying receptor interactions, enzyme inhibition, and other biological processes. Researchers are exploring its potential therapeutic applications, especially in the areas of neurochemistry and drug design, for targeting specific biological pathways.