Valinomycin

VALINOMYCIN Struktur
2001-95-8
CAS-Nr.
2001-95-8
Bezeichnung:
Valinomycin
Englisch Name:
VALINOMYCIN
Synonyma:
valinomicin;nsc122023;valamycin;-valyl)[qr];VALINOMYCIN;nsc122023[qr];valinomicin[qr];VALINOMYCIN 99%;Valinomycin,90%;Valinomycin,96%
CBNumber:
CB7199194
Summenformel:
C54H90N6O18
Molgewicht:
1111.32
MOL-Datei:
2001-95-8.mol

Valinomycin Eigenschaften

Schmelzpunkt:
187-190 °C
alpha 
D20 +31.0° (c = 1.6 in benzene)
Siedepunkt:
821.74°C (rough estimate)
Dichte
1.060
Brechungsindex
1.6400 (estimate)
Flammpunkt:
87℃
storage temp. 
2-8°C
Löslichkeit
DMSO: ≥10 mg/mL
Aggregatzustand
solid
pka
11.32±0.70(Predicted)
Farbe
white
Optische Aktivität
[α]20/D +32±2°, c = 1.6% in benzene
Wasserlöslichkeit
Soluble in DMSO at 10mg/ml. Insoluble in water
Merck 
13,9976
BRN 
78657
Stabilität:
Stable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20° for up to 3 months.
EPA chemische Informationen
Valinomycin (2001-95-8)

Sicherheit

Kennzeichnung gefährlicher Xn,T,T+,Xi
R-Sätze: 27/28-36/37/38-21/22
S-Sätze: 36-45-36/37-28-37/39-26
RIDADR  UN 2811 6.1/PG 1
WGK Germany  3
RTECS-Nr. YV9468000
10-18-21
TSCA  Yes
HazardClass  6.1(a)
PackingGroup  I
HS Code  29419090
Giftige Stoffe Daten 2001-95-8(Hazardous Substances Data)

Valinomycin Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:

R27/28:Sehr giftig bei Berührung mit der Haut und beim Verschlucken.
R36/37/38:Reizt die Augen, die Atmungsorgane und die Haut.

S-Sätze Betriebsanweisung:

S36:DE: Bei der Arbeit geeignete Schutzkleidung tragen.
S45:Bei Unfall oder Unwohlsein sofort Arzt zuziehen (wenn möglich, dieses Etikett vorzeigen).
S36/37:Bei der Arbeit geeignete Schutzhandschuhe und Schutzkleidung tragen.
S28:Bei Berührung mit der Haut sofort abwaschen mit viel . . . (vom Hersteller anzugeben).
S37/39:Bei der Arbeit geeignete Schutzhandschuhe und Schutzbrille/Gesichtsschutz tragen.
S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.

Chemische Eigenschaften

white crystalline powder

Verwenden

Valinomycin is a hydrophobic cyclodepsipeptide with potent antitumour activity. Valinomycin is a highly selective potassium ionophore and this action leads to a diverse range of profound cell membrane effects. More recently, valinomycin has found application as a biosensor to detect to detect potassium efflux.

Definition

ChEBI: A twelve-membered cyclodepsipeptide composed of three repeating D-alpha-hydroxyisovaleryl-D-valyl-L-lactoyl-L-valyl units joined in sequence. An antibiotic found in severa Streptomyces strains.

Allgemeine Beschreibung

Shiny crystalline solid. Used as an insecticide and nematocide. Not registered as a pesticide in the U.S.

Reaktivität anzeigen

VALINOMYCIN is an amide. Amides/imides react with azo and diazo compounds to generate toxic gases. Flammable gases are formed by the reaction of organic amides/imides with strong reducing agents. Amides are very weak bases (weaker than water). Imides are less basic yet and in fact react with strong bases to form salts. That is, they can react as acids. Mixing amides with dehydrating agents such as P2O5 or SOCl2 generates the corresponding nitrile. The combustion of these compounds generates mixed oxides of nitrogen (NOx).

Health Hazard

VALINOMYCIN is highly toxic orally.

Brandgefahr

When heated to decomposition, VALINOMYCIN emits toxic fumes of nitrogen oxides.

Biologische Aktivität

Selective K + ionophore (K 0.5 values are 48, 73, 75, 93 and 246 mM for K + , Rb + , Cs + , Na + and Li + respectively) that transports K + across biological and artificial lipid membranes. Inhibits Ca 2+ -ATPase activity and induces apoptosis through mitochondrial membrane depolarization, caspase-3 activation and phosphatidylserine translocation in vitro .

läuterung methode

Recrystallise valinomycin from dibutyl ether or Et2O. It is dimorphic: modification A crystallises from n-octane, and modification B crystallises from EtOH/H2O. It is soluble in pet ether, CHCl3, AcOH, BuOAc and Me2CO. [Smith et al. J Am Chem Soc 97 7242 1975, UV, IR and NMR see Brocknmann & Schmidt-Kastner Chem Ber 88 57 1955, Beilstein 27 I 9728. 17 IV 9728.]

Valinomycin Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Valinomycin Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 206)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Hebei Mojin Biotechnology Co., Ltd
+8613288715578
sales@hbmojin.com China 12453 58
career henan chemical co
+86-0371-86658258
sales@coreychem.com China 29914 58
Hebei Guanlang Biotechnology Co., Ltd.
+86-19930503282
alice@crovellbio.com China 8822 58
Chongqing Chemdad Co., Ltd
+86-023-61398051 +8613650506873
sales@chemdad.com China 39916 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427
sales@conier.com China 47465 58
Shaanxi Dideu Medichem Co. Ltd
+86-029-81138252 +86-18789408387
1057@dideu.com China 3834 58
Fuxin Pharmaceutical
+86-021-021-50872116 +8613122107989
contact@fuxinpharm.com China 10297 58
Hefei TNJ Chemical Industry Co.,Ltd.
0551-65418671
sales@tnjchem.com China 34572 58
Shaanxi Dideu Medichem Co. Ltd
+86-029-89586680 +86-18192503167
1026@dideu.com China 9604 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250
1026@dideu.com China 29525 58

2001-95-8(Valinomycin)Verwandte Suche:


  • 1,7,13,19,25,31-hexaoxa-4,10,16,22,28,34-hexaazacyclohexatriacontane-2,5,8,11,
  • 14,17,20,23,26,29,32,35-dodecone,12,24,36-trimetyl-3,6,9,15,18,21,27,30,33-non
  • akis(1-methylethyl)-[qr]
  • aleryl-d-valyl-l-lactoyl-l-valyl-d-alpha-hydroxyisovaleryl-d-valyl-l-lactoyl-l
  • antibioticn-329b
  • cyclic(d-alpha-hydroxyisovaleryl-d-valyl-l-lactoyl-l-valyl-d-alpha-hydroxyisov
  • nsc122023
  • nsc122023[qr]
  • valinomicin[qr]
  • ValinoMycin, froM StreptoMyces fulvissiMus
  • -valyl)[qr]
  • VALINOMYCIN
  • VALINOMYCIN, STREPTOMYCES FULVISSIMUS
  • POTASSIUM IONOPHORE I
  • CYCLO[-L-VAL-D-HYLVA-D-VAL-L-LAC-]3
  • CYCLO(LAC-VAL-D-HIV-D-VAL-LAC-VAL-D-HIV-D-VAL-)
  • Cyclo(L-Val-D-HyIva-D-Val-L-Lac-)3: HyIva = α-Hydroxyisovaleric acid, Lac = Lactic acid
  • VALINOMYCIN >94% PURITY
  • VALINOMYCIN READY MADE SOLUTION
  • VALINOMYCIN 99%
  • Valinomycin,90%
  • Valinomycin,96%
  • Cyclo(D-α-hydroxyisovaleryl-D-valyl-L-lactoyl-L-valyl-D-α-hydroxyisovaleryl-D-valyl-L-lactoyl-L-valyl-D-α-hydroxyisovaleryl-D-valyl-L-lactoyl-L-valyl)
  • VALINOMYCINRESEARCH GRADE
  • Potassium ionophore I,Valinomycin
  • Valinomycin,Cyclo(L-Val-D-HyIva-D-Val-L-Lac-)3: HyIva = α-Hydroxyisovaleric acid, Lac = Lactic acid
  • 1Cyclo(D-α-hydroxyisovaleryl-D-valyl-L-lactoyl-L-valyl-D-α- hydroxyisovaleryl-D-valyl-L-lactoyl-L-valyl-D-α-hydroxyisovaleryl-D-valyl-L-lactoyl-L-valyl)
  • 3,6,9,15,18,21,27,30,33-Nonaisopropyl-12,24,36-triMethyl-1,7,13,19,25,31-hexaoxa-4,10,16,22,28,34-hexaazacyclohexatriacontane-2,5,8,11,14,17,20,23,26,29,32,35-dodecone
  • VALINOMYCIN,CRYSTAL
  • Valinomycin, ≥98%(TLC),≥95%(HPLC),solid
  • Valinomycin, Streptomyces fulvissimus - CAS 2001-95-8 - Calbiochem
  • Valinomycin, 97%, from Streptomyces fulvissimus
  • VALINOMYCIN USP/EP/BP
  • Valinomycin (NSC-122023)
  • valinomicin
  • valamycin
  • 2001-95-8
  • C54H90N6O18
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