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(2S)-3-(4-phenylphenyl)-2-[[(2R)-3-phenyl-2-sulfanylpropanoyl]amino]propanoic acid , CAS No.S608850, Inhibitor of Carboxypeptidase A1 (pancreatic);Inhibitor of Neutral endopeptidase

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(2S)-3-(4-phenylphenyl)-2-[[(2R)-3-phenyl-2-sulfanylpropanoyl]amino]propanoic acid , CAS No.S608850, Inhibitor of Carboxypeptidase A1 (pancreatic);Inhibitor of Neutral endopeptidase

Moligand™

PubChem CID: 44377139

Item Number

S608850

Grouped product items
SKU	Size	Availability	Price	Qty
S608850-5mg	5mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$700.90
S608850-25mg	25mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$2,000.90

View related series

Carboxypeptidase A1 (pancreatic) Inhibitor Neutral endopeptidase Inhibitor

Basic Description

Synonyms	compound 1b
Specifications & Purity	Moligand™
Grade	Moligand™
Action Type	INHIBITOR
Mechanism of action	Inhibitor of Carboxypeptidase A1 (pancreatic);Inhibitor of Neutral endopeptidase

Associated Targets

CPA1 Tchem Carboxypeptidase A1 2 Activities

Discover Target: CPA1

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

MME Tclin Neprilysin 2 Activities

Discover Target: MME

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

ACE2 Tchem Angiotensin-converting enzyme 2 0 Activities

Discover Target: ACE2

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

ACE Tclin Angiotensin-converting enzyme 1 Activities

Discover Target: ACE

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

Names and Identifiers

IUPAC Name	(2S)-3-(4-phenylphenyl)-2-[[(2R)-3-phenyl-2-sulfanylpropanoyl]amino]propanoic acid
INCHI	InChI=1S/C24H23NO3S/c26-23(22(29)16-17-7-3-1-4-8-17)25-21(24(27)28)15-18-11-13-20(14-12-18)19-9-5-2-6-10-19/h1-14,21-22,29H,15-16H2,(H,25,26)(H,27,28)/t21-,22+/m0/s1
InChi Key	BNECOBGISSOLPT-FCHUYYIVSA-N
Canonical SMILES	S[C@@H](C(=O)N[C@H](C(=O)O)Cc1ccc(cc1)c1ccccc1)Cc1ccccc1
Isomeric SMILES	C1=CC=C(C=C1)C[C@H](C(=O)N[C@@H](CC2=CC=C(C=C2)C3=CC=CC=C3)C(=O)O)S
PubChem CID	44377139

Database links

ChEMBL Ligand	CHEMBL163454
PubChem CID	44377139

Certificates

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References

1. Deaton DN, Gao EN, Graham KP, Gross JW, Miller AB, Strelow JM. (2008) Thiol-based angiotensin-converting enzyme 2 inhibitors: P1 modifications for the exploration of the S1 subsite.. Bioorg Med Chem Lett, 18 (2): (732-7). [PMID:18078750]

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