67401-56-3

Micrococcin P1 Chemical Structure
67401-56-3

Chemical Structure

Micrococcin P1

  • CAS No.: 67401-56-3
  • Formula:C48H49N13O9S6
  • Molecular Weight:1144.37

IUPAC Name: 2'-((12Z,32Z,72Z,112Z,8S,12Z,15S)-12-ethylidene-4,15-bis((R)-1-hydroxyethyl)-8-isopropyl-6,10,14,17-tetraoxo-5,9,13,16-tetraaza-1(2,4),3,7,11(4,2)-tetrathiazola-2(3,2)-pyridinacycloheptadecaphane-26-yl)-N-((Z)-1-(((R)-2-hydroxypropyl)amino)-1-oxobut-2-en-2-yl)-[2,4'-bithiazole]-4-carboxamide

InChIKey: MQGFYNRGFWXAKA-YGVCRTKKSA-N

SMILES: C[C@H](C(N1)C2=NC(C3=NC(C4=NC(C5=NC(C(N/C(C(NC[C@H](O)C)=O)=C\C)=O)=CS5)=CS4)=CC=C3C6=NC(C(N[C@@](C(N/C(C7=NC(C(N[C@@H](C(C)C)C8=NC(C1=O)=CS8)=O)=CS7)=C\C)=O)([H])[C@H](O)C)=O)=CS6)=CS2)O

Biological Activity: Micrococcin P1 is a macrocyclic peptide antibiotic and is a potent hepatitis C virus (HCV) inhibitor with an EC50 range of 0.1-0.5 μM[1]. Micrococcin P1 has in vitro antibacterial activity against Gram-positive bacterial strains. The MIC values of Micrococcin P1 against S. aureus 1974149, E. faecalis 1674621 and S. pyogenes 1744264 are 2 μg/mL, 1 μg/mL and 1 μg/mL, respectively[2]. Micrococcin P1 is also a potent inhibitor of the malaria parasite Plasmodium falciparum[3].

Cat. No. Product Name Purity Description Pricing
HY-125728
Micrococcin P1 99.0% Micrococcin P1 is a macrocyclic peptide antibiotic and is a potent hepatitis C virus (HCV) inhibitor with an EC50 range of 0.1-0.5 μM. Micrococcin P1 has in vitro antibacterial activity against Gram-positive bacterial strains. The MIC values of Micrococcin P1 against S. aureus 1974149, E. faecalis 1674621 and S. pyogenes 1744264 are 2 μg/mL, 1 μg/mL and 1 μg/mL, respectively. Micrococcin P1 is also a potent inhibitor of the malaria parasite Plasmodium falciparum.
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This product is a controlled substance and not for sale in your territory.

This product is not for sale in your territory.

This compound is listed in the SVHC (Substances of Very High Concern) candidate list of ECHA (European Chemicals Agency).

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References