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SM-337 , CAS No.S613630, Antagonist of baculoviral IAP repeat containing 2;Antagonist of baculoviral IAP repeat containing 3;Antagonist of X-linked inhibitor of apoptosis

  • Moligand™
Item Number
S613630
Grouped product items
SKUSizeAvailabilityPrice Qty
S613630-5mg
5mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$921.90
S613630-25mg
25mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$3,224.90
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baculoviral IAP repeat containing 2 Antagonist baculoviral IAP repeat containing 3 Antagonist X-linked inhibitor of apoptosis Antagonist

Basic Description

SynonymsSM-337|1071992-61-4|CHEMBL504559|(5S,8S,10aR)-N-benzhydryl-5-[[(2S)-2-(methylamino)propanoyl]amino]-6-oxo-3-(2-phenylacetyl)-1,2,4,5,8,9,10,10a-octahydropyrrolo[1,2-a][1,5]diazocine-8-carboxamide|Pyrrolo[1,2-a][1,5]diazocine-8-carboxamide, N-(diphenylmeth
GradeMoligand™
Action TypeANTAGONIST
Mechanism of actionAntagonist of baculoviral IAP repeat containing 2;Antagonist of baculoviral IAP repeat containing 3;Antagonist of X-linked inhibitor of apoptosis

Associated Targets

BIRC8 Tchem Baculoviral IAP repeat-containing protein 8 1 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

BIRC2 Tchem Baculoviral IAP repeat-containing protein 2 4 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

BIRC3 Tchem Baculoviral IAP repeat-containing protein 3 3 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

XIAP Tchem E3 ubiquitin-protein ligase XIAP 3 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name (5S,8S,10aR)-N-benzhydryl-5-[[(2S)-2-(methylamino)propanoyl]amino]-6-oxo-3-(2-phenylacetyl)-1,2,4,5,8,9,10,10a-octahydropyrrolo[1,2-a][1,5]diazocine-8-carboxamide
INCHI InChI=1S/C35H41N5O4/c1-24(36-2)33(42)37-29-23-39(31(41)22-25-12-6-3-7-13-25)21-20-28-18-19-30(40(28)35(29)44)34(43)38-32(26-14-8-4-9-15-26)27-16-10-5-11-17-27/h3-17,24,28-30,32,36H,18-23H2,1-2H3,(H,37,42)(H,38,43)/t24-,28+,29-,30-/m0/s1
InChi Key YBYZHVZWINISJO-XPSCAIQQSA-N
Canonical SMILES CN[C@H](C(=O)N[C@H]1CN(CC[C@@H]2N(C1=O)[C@@H](CC2)C(=O)NC(c1ccccc1)c1ccccc1)C(=O)Cc1ccccc1)C
Isomeric SMILES C[C@@H](C(=O)N[C@H]1CN(CC[C@H]2CC[C@H](N2C1=O)C(=O)NC(C3=CC=CC=C3)C4=CC=CC=C4)C(=O)CC5=CC=CC=C5)NC
PubChem CID 25172871

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Related Documents

 SDS

 Specification Sheet

References

1. Peng Y, Sun H, Nikolovska-Coleska Z, Qiu S, Yang CY, Lu J, Cai Q, Yi H, Kang S, Yang D et al..  (2008)  Potent, orally bioavailable diazabicyclic small-molecule mimetics of second mitochondria-derived activator of caspases..  J Med Chem,  51  (24): (8158-62).  [PMID:19049347]

Solution Calculators

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