sucunamostat - Moligand™ , Inhibitor of transmembrane serine protease 15, CAS No.1802888-04-5, Inhibitor of transmembrane serine protease 15

CAS: 1802888-04-5 Cat. No.: S613746 PubChem CID: 91827404

GRADE & PURITY Moligand™

Synonyms

V4JYY6ESD3 | HY-132841 | 1802888-04-5 | GTPL11683 | L-Aspartic acid, N-(2-((3S)-6-((4-((aminoiminomethyl)amino)benzoyl)oxy)-2,3-dihydro-3-benzofuranyl)acetyl)- | Sucunamostat [INN] | (2S)-2-[[2-[(3S)-6-[4-(Diaminomethylideneamino)benzoyl]oxy-2,3-dihydro-1

Storage

Room temperature

Specifications

Synonyme

V4JYY6ESD3 | HY-132841 | 1802888-04-5 | GTPL11683 | L-Aspartic acid, N-(2-((3S)-6-((4-((aminoiminomethyl)amino)benzoyl)oxy)-2,3-dihydro-3-benzofuranyl)acetyl)- | Sucunamostat [INN] | (2S)-2-[[2-[(3S)-6-[4-(Diaminomethylideneamino)benzoyl]oxy-2,3-dihydro-1

Spezifikationen & Reinheit

Moligand™

Storage

Room temperature

Note

Moligand™

Aktionsart

INHIBITOR

Mechanismus der Wirkung

Inhibitor of transmembrane serine protease 15

Namen und Kennungen

Kanonisches Lächeln

N(C(=N)N)c1ccc(C(=O)Oc2cc3c([C@@H](CO3)CC(=O)N[C@@H](CC(=O)O)C(=O)O)cc2)cc1

IUPAC Name

(2S)-2-[[2-[(3S)-6-[4-(Diaminomethylideneamino)benzoyl]oxy-2,3-dihydro-1-benzofuran-3-yl]acetyl]amino]butanedioic acid

InChIKey

PUZUTMLAAWVCCV-WBMJQRKESA-N

INCHI

1S/C22H22N4O8/c23-22(24)25-13-3-1-11(2-4-13)21(32)34-14-5-6-15-12(10-33-17(15)8-14)7-18(27)26-16(20(30)31)9-19(28)29/h1-6,8,12,16H,7,9-10H2,(H,26,27)(H,28,29)(H,30,31)(H4,23,24,25)/t12-,16+/m1/s1

Isomere SMILES

C1[C@H](C2=C(O1)C=C(C=C2)OC(=O)C3=CC=C(C=C3)N=C(N)N)CC(=O)N[C@@H](CC(=O)O)C(=O)O

PubChem CID

91827404

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Klasse Carboxylic acids and derivatives
      • Subclass Amino acids, peptides, and analogues
        • Ebene5 Amino acids and derivatives
          • Ebene6 Alpha amino acids and derivatives
            • Ebene7 Aspartic acid and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Klasse: Carboxylic acids and derivatives
• Subclass: Amino acids, peptides, and analogues
• Intermediate Tree Nodes: Amino acids and derivatives - Alpha amino acids and derivatives
• Direct Parent: Aspartic acid and derivatives
• Alternative Parents: N-acyl-L-alpha-amino acids Guanidinobenzoic acids and derivatives Benzoic acid esters Phenol esters Coumarans Benzoyl derivatives Alkyl aryl ethers Dicarboxylic acids and derivatives Secondary carboxylic acid amides Carboxylic acid esters Guanidines Carboxylic acids Propargyl-type 1,3-dipolar organic compounds Oxacyclic compounds Carbonyl compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Aspartic acid or derivatives - N-acyl-alpha-amino acid - N-acyl-alpha amino acid or derivatives - Guanidinobenzoic acid or derivatives - N-acyl-l-alpha-amino acid - Phenol ester - Benzoate ester - Benzoic acid or derivatives - Coumaran - Benzoyl - Alkyl aryl ether - Dicarboxylic acid or derivatives - Benzenoid - Monocyclic benzene moiety - Carboxylic acid ester - Secondary carboxylic acid amide - Guanidine - Carboxamide group - Oxacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Carboxylic acid - Propargyl-type 1,3-dipolar organic compound - Ether - Carbonyl group - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as aspartic acid and derivatives. These are compounds containing an aspartic acid or a derivative thereof resulting from reaction of aspartic acid at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

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TMPRSS15 Tchem Enteropeptidase (0 Activities)

Discover Target: TMPRSS15

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

Wirkungsmechanismen

Häufig gestellte Fragen

What is Moligand??

Moligand? is one of Aladdin Scientific's premium product lines, formulated for high-purity applications across multiple workflows. Compared to standard grades in the same workflow, Moligand? products typically offer tighter specifications, more rigorous QC, and stronger lot-to-lot consistency.

How should this product be stored?

Store at room temperature.

What are the CAS number, molecular formula and molecular weight?

The CAS Number is 1802888-04-5. InChIKey PUZUTMLAAWVCCV-WBMJQRKESA-N.

What documentation is provided?

Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.