enniatin B1

enniatin B1 Struktur
19914-20-6
CAS-Nr.
19914-20-6
Englisch Name:
enniatin B1
Synonyma:
enniatin B1;2-(N-Methyl-L-isoleucine)enniatin B;3-Butan-2-yl-4,10,16-trimethyl-6,9,12,15,18-penta(propan-2-yl)-1,7,13-trioxa-4,10,16-triazacyclooctadecane-2,5,8,11,14,17-hexone;Cyclo[(2R)-2-hydroxy-3-methylbutanoyl-N-methyl-L-isoleucyl-(2R)-2-hydroxy-3-methylbutanoyl-N-methyl-L-valyl-(2R)-2-hydroxy-3-methylbutanoyl-N-methyl-L-valyl]
CBNumber:
CB12079102
Summenformel:
C34H59N3O9
Molgewicht:
653.85
MOL-Datei:
19914-20-6.mol

enniatin B1 Eigenschaften

Schmelzpunkt:
178.5 °C
Siedepunkt:
833.8±65.0 °C(Predicted)
Dichte
1.031±0.06 g/cm3(Predicted)
storage temp. 
-20°C
Löslichkeit
DMSO: soluble10mg/mL
Aggregatzustand
White to off-white crystalline solid.
pka
-1.45±0.70(Predicted)

Sicherheit

Kennzeichnung gefährlicher T
R-Sätze: 23/24/25
S-Sätze: 45
RIDADR  2811
WGK Germany  3
HazardClass  6.1(a)
PackingGroup  I
HS Code  2941900000

enniatin B1 Chemische Eigenschaften,Einsatz,Produktion Methoden

Verwenden

Enniatins are a family of depsipeptide ionophores, produced several Fusarium species. More recently, the effects of the enniatins on acyl-CoA cholesterol transferase, transporters and the selectivity of their antitumour action have received more focus. Enniatin B1 is one of four major analogues of the enniatin complex and has not previously been available for investigation.

Biochem/physiol Actions

Enniatins are a group of cyclohexadepsipeptide mycotoxins produced by Gnomonia errabuda and several Fusaria species, with phytotoxic, antibiotic, and insecticidal activities. Enniatins function as ionophors by their incorporation into the cellular membrane to form dimeric structures that transport monovalent ions across the membrane (especially the mitochondrial membranes) affecting oxidative phosphorylation uncoupling. It has been demonstrated that enniatins have a cytotoxic effect on human cancer cells. Furthermore, incubation of H4IIE hepatoma cells with enniatins strongly diminished phosphorylation of the ERK (p44/p42). Enniatins B and B1 inhibit the multi-drug resistance transporter Pdr5p from Saccharomyces cerevisiae, indicating their beneficial potential in cases of drug resistant patients.

enniatin B1 Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


enniatin B1 Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 94)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795
ivan@atkchemical.com China 32760 60
Hubei Jusheng Technology Co.,Ltd.
18871490254
linda@hubeijusheng.com CHINA 28180 58
Shaanxi Pioneer Biotech Co., Ltd .
+8613259417953
sales@pioneerbiotech.com China 3000 58
BOC Sciences
+1-631-485-4226
inquiry@bocsci.com United States 19553 58
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000
marketing@targetmol.com United States 19892 58
LEAPCHEM CO., LTD.
+86-852-30606658
market18@leapchem.com China 43348 58
Aladdin Scientific
+1-+1(833)-552-7181
sales@aladdinsci.com United States 52927 58
Nanjing Shizhou Biology Technology Co.,Ltd 025-85560043 13675144456
sean.lv@synzest.com China 11442 58
Chembest Research Laboratories Limited 021-20908456
sales@BioChemBest.com China 6008 61
BioBioPha Co., Ltd. 0871-65217109 13211707573;
y.liu@mail.biobiopha.com China 5654 65

19914-20-6()Verwandte Suche:


  • enniatin B1
  • 2-(N-Methyl-L-isoleucine)enniatin B
  • 3-Butan-2-yl-4,10,16-trimethyl-6,9,12,15,18-penta(propan-2-yl)-1,7,13-trioxa-4,10,16-triazacyclooctadecane-2,5,8,11,14,17-hexone
  • Cyclo[(2R)-2-hydroxy-3-methylbutanoyl-N-methyl-L-isoleucyl-(2R)-2-hydroxy-3-methylbutanoyl-N-methyl-L-valyl-(2R)-2-hydroxy-3-methylbutanoyl-N-methyl-L-valyl]
  • 19914-20-6
  • C34H59N3O9
  • Antibiotic
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