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NIKKOMYCIN Z

NIKKOMYCIN Z Structure
CAS No.
59456-70-1
Chemical Name:
NIKKOMYCIN Z
Synonyms
NIKKOMYCIN;huaguamycin;neopolyoxinc;NIKKOMYCIN Z;(2s-(2r*,3r*,4r*))-l);NIKKOMYCIN Z, STREPTOMYCES TENDAE;Nikkomycin Z, Sterptomyces tendae;nikkomycin Z from streptomyces tendae;5-((2-amino-4-hydroxy-4-(5-hydroxy-2-pyridinyl)-3-beta-d-allofuranuronicaci;5-((2-Amino-4-hydroxy-4-(5-hydroxy-2-pyridinyl)-3-beta-d-allofuranuronicacid
CBNumber:
CB0767000
Molecular Formula:
C20H25N5O10
Molecular Weight:
495.44
MOL File:
59456-70-1.mol
Modify Date:
2024/7/2 8:54:58

NIKKOMYCIN Z Properties

Density 1.646±0.06 g/cm3(Predicted)
storage temp. 2-8°C
solubility H2O: soluble5mg/mL
form Solid
pka 2.70±0.10(Predicted)
color White to off-white
Water Solubility Water : ≥ 100 mg/mL (201.84 mM)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H335-H315-H319
Precautionary statements  P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36
WGK Germany  3
RTECS  BA2928200
10

NIKKOMYCIN Z price More Price(1)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) N8028 Nikkomycin Z from Streptomyces tendae ≥90% (HPLC) 59456-70-1 5MG ₹26726.93 2022-06-14 Buy
Product number Packaging Price Buy
N8028 5MG ₹26726.93 Buy

NIKKOMYCIN Z Chemical Properties,Uses,Production

Description

Nucleoside-type antibiotic isolated from culture filtrates of Streptomyces tendae (19). Some analogs were also prepared by mutasynthesis, utilizing a uracil auxotroph of S. tendae.

Uses

Nikkomycins inhibit the growth of various plant pathogenic fungi but are inactive against bacteria and yeasts. Too susceptible to photodegradation by sunlight to be used in field application, and thus not developed commercially for agricultural use. Among the nikkomycins, nikkomycin Z is an orally active antifungal therapeutic agent for coccidioidomycosis. It is a competitive chitin synthase inhibitor that has been evaluated in mouse models for coccidioidomycosis.

Definition

ChEBI: A uridine-based nucleoside-peptide antibiotic which inhibits fungal chitin biosynthesis by inhibiting chitin synthase.

Pharmacology

By inhibiting chitin synthetase in fungi, nikkomycins inhibit cell wall synthesis, ultimately causing fungal cells to swell and burst.

Metabolism

There are no detailed reports on metabolism/transformation of nikkomycins in the environment.

NIKKOMYCIN Z Preparation Products And Raw materials

Raw materials

Preparation Products

NIKKOMYCIN Z Suppliers

Global( 37)Suppliers
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AFINE CHEMICALS LIMITED +86-0571-85134551 China 15395 58 Inquiry
Hangzhou MolCore BioPharmatech Co.,Ltd. +86-057181025280; +8617767106207 China 49739 58 Inquiry
TargetMol Chemicals Inc. +1-781-999-5354 United States 19973 58 Inquiry
SUZHOU SENFEIDA CHEMICAL CO.,LTD +86-0512-83500002 +8615195660023 China 23053 58 Inquiry
Shaanxi Cuikang Pharmaceutical Technology Co., Ltd +86-19164747840 +86-13119157289 China 2971 58 Inquiry
Aladdin Scientific +1-+1(833)-552-7181 United States 52927 58 Inquiry
RD International Technology Co., Limited 18024082417 China 9274 58 Inquiry
TargetMol Chemicals Inc. 15002134094 China 28091 58 Inquiry
Shanghai Maclean Biochemical Technology Co., LTD 021-50706066 15221275939 China 29803 58 Inquiry
MedChemExpress 021-58955995 United States 6398 58 Inquiry

Related articles

  • Mechanism of action of Nikkomycin Z
  • Nikkomycin Z is an experimental compound with antifungal properties. Like all nikkomycins, it consists of a pyrimidine nucleos....
  • Mar 31,2022
NIKKOMYCIN NIKKOMYCIN Z NIKKOMYCIN Z, STREPTOMYCES TENDAE (2s-(2r*,3r*,4r*))-l) 5-((2-amino-4-hydroxy-4-(5-hydroxy-2-pyridinyl)-3-beta-d-allofuranuronicaci methyl-1-oxobutyl)amino)-1,5-dideoxy-1-(3,4-dihydro-2,4-dioxo-1(2h)-pyrimidiny neopolyoxinc nikkomycin Z from streptomyces tendae Nikkomycin Z, Sterptomyces tendae 5-[[(2S,3S,4S)-2-Amino-4-hydroxy-4-(5-hydroxy-2-pyridinyl)-3-methyl-1-oxobutyl]amino]-1-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-1,5-dideoxy-β-D-allofuranuronic acid 5-[[(2S,3S,4S)-2-Amino-4-hydroxy-4-(5-hydroxy-2-pyridinyl)-3-methyl-1-oxobutyl]amino]-1-(3,4-dihydro-2,4-dioxopyrimidin-1(2H)-yl)-1,5-dideoxy-β-D-allofuranuronic acid 5-((2-Amino-4-hydroxy-4-(5-hydroxy-2-pyridinyl)-3-beta-d-allofuranuronicacid β-D-Allofuranuronic acid, 5-[[(2S,3S,4S)-2-amino-4-hydroxy-4-(5-hydroxy-2-pyridinyl)-3-methyl-1-oxobutyl]amino]-1,5-dideoxy-1-(3,4-dihydro-2,4-dioxo-1(2H)-pyrimidinyl)- huaguamycin 59456-70-1 C20H25N5O10 BioChemical Antibiotics Antibiotics A to Z Antibiotics N-S AntifungalGlycobiology InhibitorsAntibiotics Peptidyl NucleosidesMore...Close... Inhibitors and Substrates Peptidyl Nucleosides Antibiotics Antibiotics A to Antibiotics N-SAntibiotics AntifungalAntibiotics Chemical Structure Class Inhibits an EnzymeAntibiotics Interferes with Cell Wall SynthesisAntibiotics Mechanism of Action Spectrum of Activity