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Kendomycin from Streptomyces violaceoruber_Molecular_structure_CAS_183202-73-5)
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Kendomycin from Streptomyces violaceoruber

Catalog No. K1513 Name Sigma Aldrich
CAS Number 183202-73-5 Website http://www.sigmaaldrich.com
M. F. C32H61N13O9 Telephone 1-800-521-8956
M. W. 771.90844 Fax
Purity Email
Storage Chembase ID: 155629

SYNONYMS

IUPAC name
2-{2-[2-(2-{2-[2-(2-amino-4-methylpentanamido)-5-carbamimidamidopentanamido]-5-carbamimidamidopentanamido}propanamido)-3-hydroxypropanamido]-3-methylbutanamido}propanoic acid
IUPAC Traditional name
2-{2-[2-(2-{2-[2-(2-amino-4-methylpentanamido)-5-carbamimidamidopentanamido]-5-carbamimidamidopentanamido}propanamido)-3-hydroxypropanamido]-3-methylbutanamido}propanoic acid
Synonyms
(-)-TAN 2162

DATABASE IDS

CAS Number 183202-73-5
MDL Number MFCD00076711
PubChem SID 24896208

PROPERTIES

Empirical Formula (Hill Notation) C29H42O6
Apperance solid
MSDS Link Download
Personal Protective Equipment Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Storage Temperature -20°C
German water hazard class 3

DETAILS

Description (English)
Biochem/physiol Actions
Potent endothelin receptor antagonist. Antiosteoporotic compound. Shows also remarkable antibacterial and cytotoxic activity. A putative cellular target for cytotoxicity has been identified: inhibition or altered regulation of the proteasome.1
Description (简体中文)
Biochem/physiol Actions
Potent endothelin receptor antagonist. Antiosteoporotic compound. Shows also remarkable antibacterial and cytotoxic activity. A putative cellular target for cytotoxicity has been identified: inhibition or altered regulation of the proteasome.1

REFERENCES