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VALINOMYCIN

VALINOMYCIN Structure
CAS No.
2001-95-8
Chemical Name:
VALINOMYCIN
Synonyms
valinomicin;nsc122023;valamycin;-valyl)[qr];VALINOMYCIN;nsc122023[qr];valinomicin[qr];VALINOMYCIN 99%;Valinomycin,90%;Valinomycin,96%
CBNumber:
CB7199194
Molecular Formula:
C54H90N6O18
Molecular Weight:
1111.32
MOL File:
2001-95-8.mol
MSDS File:
SDS
Modify Date:
2023/8/30 13:35:17

VALINOMYCIN Properties

Melting point 187-190 °C
alpha D20 +31.0° (c = 1.6 in benzene)
Boiling point 821.74°C (rough estimate)
Density 1.060
refractive index 1.6400 (estimate)
Flash point 87℃
storage temp. 2-8°C
solubility DMSO: ≥10 mg/mL
form solid
pka 11.32±0.70(Predicted)
color white
optical activity [α]20/D +32±2°, c = 1.6% in benzene
Water Solubility Soluble in DMSO at 10mg/ml. Insoluble in water
Merck 13,9976
BRN 78657
Stability Stable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20° for up to 3 months.
EPA Substance Registry System Valinomycin (2001-95-8)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS06
Signal word  Danger
Hazard statements  H300+H310
Precautionary statements  P262-P280-P301+P310+P330-P302+P352+P310
Hazard Codes  Xn,T,T+,Xi
Risk Statements  27/28-36/37/38-21/22
Safety Statements  36-45-36/37-28-37/39-26
RIDADR  UN 2811 6.1/PG 1
WGK Germany  3
RTECS  YV9468000
10-18-21
TSCA  Yes
HazardClass  6.1(a)
PackingGroup  I
HS Code  29419090
NFPA 704
0
4 0

VALINOMYCIN price More Price(11)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) V0627 Valinomycin ≥98% (TLC), ≥90% (HPLC) 2001-95-8 10MG ₹9157.95 2022-06-14 Buy
Sigma-Aldrich(India) V0627 Valinomycin ≥98% (TLC), ≥90% (HPLC) 2001-95-8 25MG ₹16107.6 2022-06-14 Buy
Sigma-Aldrich(India) V0627 Valinomycin ≥98% (TLC), ≥90% (HPLC) 2001-95-8 100MG ₹40994.28 2022-06-14 Buy
Sigma-Aldrich(India) V3639 Valinomycin Ready Made Solution, ~1?mg/mL in DMSO 2001-95-8 5ML ₹10267.6 2022-06-14 Buy
Sigma-Aldrich(India) V0627 Valinomycin ≥98% (TLC), ≥90% (HPLC) 2001-95-8 500MG ₹192988.1 2022-06-14 Buy
Product number Packaging Price Buy
V0627 10MG ₹9157.95 Buy
V0627 25MG ₹16107.6 Buy
V0627 100MG ₹40994.28 Buy
V3639 5ML ₹10267.6 Buy
V0627 500MG ₹192988.1 Buy

VALINOMYCIN Chemical Properties,Uses,Production

Chemical Properties

white crystalline powder

Uses

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.

General Description

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

Reactivity Profile

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.

Fire Hazard

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

Biological Activity

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 .

Purification Methods

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 Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 207)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
Sisco Research Laboratories Pvt. Ltd. +91-22-4268 5800 Mumbai, India 4317 58 Inquiry
Triveni chemicals 08048762458 New Delhi, India 6093 58 Inquiry
CLEARSYNTH LABS LTD. +91-22-45045900 Hyderabad, India 6351 58 Inquiry
CHEMSWORTH +91-261-2397244 New Delhi, India 6707 30 Inquiry
Maas Pharma Chemicals +91-9958666224 Delhi, India 1607 58 Inquiry
Anand Agencies 91-20-24454597 Maharashtra, India 2337 58 Inquiry
HiMedia Laboratories 91-22-61471919 Maharashtra, India 1843 58 Inquiry
Hebei Mojin Biotechnology Co., Ltd +86 13288715578 +8613288715578 China 12460 58 Inquiry
career henan chemical co +86-0371-86658258 +8613203830695 China 29900 58 Inquiry
Hebei Guanlang Biotechnology Co., Ltd. +86-19930503282 China 8828 58 Inquiry

VALINOMYCIN Spectrum

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 (3S,6S,9R,12R,15S,18S,21R,24R,27S,30S,33R,36R)-6,18,30-trimethyl-3,9,12,15,21,24,27,33,36-nonakis(propan-2-yl)-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 2001-95-8 C54H90N6O18 BioChemical Analytical Chromatography Product Catalog Antibiotics A to Z Antibiotics Antibiotics T-Z Ionophores Potentiometric for ISE Ion Sensor Materials antibiotic Agro-Products Inhibitors Peptides