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(2S)-1-[(2R)-2-(benzylsulfonylamino)-5-(diaminomethylideneamino)pentanoyl]-N-[(4-carbamimidoylphenyl)methyl]pyrrolidine-2-carboxamide , CAS No.S609346, Inhibitor of transmembrane serine protease 11D;Inhibitor of transmembrane serine protease 2

  • Moligand™
Item Number
S609346
Grouped product items
SKUSizeAvailabilityPrice Qty
S609346-5mg
5mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$700.90
S609346-25mg
25mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$2,000.90
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transmembrane serine protease 11D Inhibitor transmembrane serine protease 2 Inhibitor

Basic Description

Synonymscompound 5
GradeMoligand™
Action TypeINHIBITOR
Mechanism of actionInhibitor of transmembrane serine protease 11D;Inhibitor of transmembrane serine protease 2

Associated Targets

F10 Tclin Coagulation factor X 1 Activities

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

ST14 Tchem Suppressor of tumorigenicity 14 protein 1 Activities

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

TMPRSS2 Tchem Transmembrane protease serine 2 2 Activities

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

TMPRSS11D Tchem Transmembrane protease serine 11D 2 Activities

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

TMPRSS6 Tchem Transmembrane protease serine 6 1 Activities

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

PLG Tclin Plasminogen 1 Activities

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

KLKB1 Tclin Plasma kallikrein 1 Activities

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

F2 Tclin Prothrombin 1 Activities

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

Names and Identifiers

IUPAC Name (2S)-1-[(2R)-2-(benzylsulfonylamino)-5-(diaminomethylideneamino)pentanoyl]-N-[(4-carbamimidoylphenyl)methyl]pyrrolidine-2-carboxamide
INCHI InChI=1S/C26H36N8O4S/c27-23(28)20-12-10-18(11-13-20)16-32-24(35)22-9-5-15-34(22)25(36)21(8-4-14-31-26(29)30)33-39(37,38)17-19-6-2-1-3-7-19/h1-3,6-7,10-13,21-22,33H,4-5,8-9,14-17H2,(H3,27,28)(H,32,35)(H4,29,30,31)/t21-,22+/m1/s1
InChi Key QKFCYPKTTJCUSZ-YADHBBJMSA-N
Canonical SMILES NC(=NCCC[C@H](C(=O)N1CCC[C@H]1C(=O)NCc1ccc(cc1)C(=N)N)NS(=O)(=O)Cc1ccccc1)N
Isomeric SMILES C1C[C@H](N(C1)C(=O)[C@@H](CCCN=C(N)N)NS(=O)(=O)CC2=CC=CC=C2)C(=O)NCC3=CC=C(C=C3)C(=N)N
PubChem CID 46899577

Certificates

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Related Documents

 SDS

 Specification Sheet

References

1. Sielaff F, Böttcher-Friebertshäuser E, Meyer D, Saupe SM, Volk IM, Garten W, Steinmetzer T.  (2011)  Development of substrate analogue inhibitors for the human airway trypsin-like protease HAT..  Bioorg Med Chem Lett,  21  (16): (4860-4).  [PMID:21741839]

Solution Calculators

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