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ChemicalBook >> CAS DataBase List >>NONACTIN

NONACTIN

CAS No.
6833-84-7
Chemical Name:
NONACTIN
Synonyms
3584-a;a-5584;e-79-c;n-329-a;NONACTIN;ta-25-m-i;fh-3582-a;POLYNACTIN;WERRAMYCIN A;AMMONIUM IONOPHORE
CBNumber:
CB2424675
Molecular Formula:
C40H64O12
Molecular Weight:
736.93
MDL Number:
MFCD00043039
MOL File:
6833-84-7.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 00:28:50
Product description Number Pack Size Price
Ammonium ionophore I Selectophore 09877 50mg $430
Ammonium ionophore I Selectophore 09877 250mg $1960
Nonactin, Monactin, and Dinactin Mixture ≥95%(mixtureofhomologues) 19468 5mg $54
Nonactin, Monactin, and Dinactin Mixture ≥95%(mixtureofhomologues) 19468 10mg $96
Nonactin, Monactin, and Dinactin Mixture ≥95%(mixtureofhomologues) 19468 25mg $209
More product size

NONACTIN Properties

Melting point 147-148°
Boiling point 890.6±65.0 °C(Predicted)
Density 1.11-1.15 g/cm3
storage temp. 2-8°C
solubility chloroform: soluble10mg/mL
form White to off-white crystalline solid.
color white to faint yellow
Sensitive Moisture Sensitive
Merck 13,6709
BRN 76434
Stability Stable for 1 year from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20° for up to 2 months.
InChIKey RMIXHJPMNBXMBU-QIIXEHPYSA-N
EWG's Food Scores 1
FDA UNII TTP24WX8P7
UNSPSC Code 26111700
NACRES NB.61

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P271-P280
PPE Eyeshields, Gloves, type N95 (US)
Hazard Codes  Xi
Safety Statements  22-24/25
WGK Germany  3
RTECS  RH1685000
10-21
HS Code  29321900
Storage Class 11 - Combustible Solids
Toxicity LD50 intravenous in mouse: 246mg/kg

NONACTIN price More Price(50)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 09877 Ammonium ionophore I Selectophore 6833-84-7 50mg $430 2026-04-30 Buy
Sigma-Aldrich 09877 Ammonium ionophore I Selectophore 6833-84-7 250mg $1960 2026-04-30 Buy
Cayman Chemical 19468 Nonactin, Monactin, and Dinactin Mixture ≥95%(mixtureofhomologues) 5mg $54 2026-04-30 Buy
Cayman Chemical 19468 Nonactin, Monactin, and Dinactin Mixture ≥95%(mixtureofhomologues) 10mg $96 2026-04-30 Buy
Cayman Chemical 19468 Nonactin, Monactin, and Dinactin Mixture ≥95%(mixtureofhomologues) 25mg $209 2026-04-30 Buy
Product number Packaging Price Buy
09877 50mg $430 Buy
09877 250mg $1960 Buy
19468 5mg $54 Buy
19468 10mg $96 Buy
19468 25mg $209 Buy

NONACTIN Chemical Properties,Uses,Production

Description

Nonactin (6833-84-7) is a monovalent cation ionophore with high selectivity for NH4+ and K+ .1 Upregulates levels of mitochondrial stress proteins HSP58 and GRP75.2 Nonactin abolishes mitochondrial membrane potential.3

Chemical Properties

Light yellow powder

Uses

Nonactin is an ionophore antiobiotic that selectively binds K+and NH4+.

Uses

Nonactin is the smallest member of the macrotetrolide complex produced by a range of Streptomyces species. Originally the name, nonactin, reflected the lack of biological activity. The literature is confusing in this respect, as virtually all sources of nonactin are contaminated with small amounts of the much more active monactin. The BioAustralis nonactin has been purified to remove traces of other biologically-active macrotetrolides. Like the other macrotetrolides, nonactin is a monovalent cation ionophore with high selectivity for ammonium and potassium.

Definition

ChEBI: Nonactin is a macrotetrolide.

Biological Activity

Monovalent cation ionophore that displays selectivity for K + and NH 4 + (K + = NH 4 + > Na + > Mg 2+ > Li + >> Ca 2+ for nonactin-EVA sensor). Induces cation transport across artificial membranes. Also inhibits P-glycoprotein-mediated efflux of chemotherapeutic agents in multiple-drug resistant cancer cells. Antibiotic.

Purification Methods

This macrotetrolide antibiotic crystallises from MeOH as colourless needles and is dried at 90o/20hours/high vacuum. [Cordaz et al. Helv Chim Acta 38 1445 1955, crystal structure: Dobler Helv Chim Acta 55 1371 1972, Gambos et al. Tetrahedron Lett 3391 1975, Beilstein 19/12 V 751.]

Background

The antibiotic Nonactin is an ionophore that binds and transports monovalent cations across membranes through passive diffusion. Nonactin displays both antibacterial and anti-tumor activities, and inhibits drug efflux in multiple drug resistant cancers. Naturally occurring Nonactin is composed of four monomers of Nonactic acid, comprised of an equal number of and monomers. The antibiotic properties of Nonactin result from its ability to form stable complexes with monovalent cations; artificial Nonactin tetramers, comprised of either all or all Nonactic acid monomers, lack ion binding ability and are less potent antibiotics. Treatment of erythrocytes with Nonactin leads to suicidal erythrocyte death as evidenced by the shrinking of erythrocytes and translocation of phosphatidylserine from the erythrocyte interior to the cell surface. Nonactin selectively induces apoptosis and results in tumor regression in a β-catenin mutant HCT 116 xenograft model, and can inhibit the surface expression of endogenous HSP60.

References

[1] CARLOS ALEXANDRE BORGES GARCIA  Graciliano de O N  Laércio Rover Júnior. Determination of potassium ions in pharmaceutical samples by FIA using a potentiometric electrode based on ionophore nonactin occluded in EVA membrane[J]. Journal of pharmaceutical and biomedical analysis, 2003, 31 1: Pages 11-18. DOI:10.1016/s0731-7085(02)00598-8
[2] L. MIZZEN. Identification, characterization, and purification of two mammalian stress proteins present in mitochondria, grp 75, a member of the hsp 70 family and hsp 58, a homolog of the bacterial groEL protein.[J]. The Journal of Biological Chemistry, 1989, 8 1: 20664-20675. DOI:10.1016/s0021-9258(19)47115-9
[3] A K DUDANI. Effects of antimitotic and antimitochondrial agents on the cellular distribution of microtubules and mitochondria.[J]. Cytobios, 1990, 63 253: 95-108.

NONACTIN Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 138)Suppliers
Supplier Tel Email Country ProdList Advantage
career henan chemical co
+86-0371-86658258 +8613203830695 factory@coreychem.com China 29792 58
Shaanxi Dideu Medichem Co. Ltd
+86-029-89586680 +86-18192503167 1026@dideu.com China 9996 58
BOC Sciences
16314854226; +16314854226 inquiry@bocsci.com United States 19853 58
GIHI CHEMICALS CO.,LIMITED
+86-571-86217390; +8618058761490 info@gihichemicals.com China 49969 58
Shanghai Acmec Biochemical Technology Co., Ltd.
+86-18621343501; +undefined18621343501 product@acmec-e.com China 33324 58
Aladdin Scientific
tp@aladdinsci.com United States 57505 58
SHANGHAI KEAN TECHNOLOGY CO., LTD.
+8613817748580 cooperation@kean-chem.com China 40066 58
J & K SCIENTIFIC LTD. 18210857532; 18210857532 jkinfo@jkchemical.com China 96815 76
3B Pharmachem (Wuhan) International Co.,Ltd. 821-50328103-801 18930552037 3bsc@sina.com China 15838 69
Beijing HwrkChemical Technology Co., Ltd 89508211 18501085097 sales.bj@hwrkchemical.com China 9416 55

View Lastest Price from NONACTIN manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
NONACTIN pictures 2019-12-26 NONACTIN
6833-84-7
$1.00 1g ≥98% Career Henan Chemical Co
  • NONACTIN pictures
  • NONACTIN
    6833-84-7
  • $1.00
  • ≥98%
  • Career Henan Chemical Co
ta-25-m-i NONACTIN NONACTIN, STREPTOMYCES GRISEUS POLYNACTIN NONACTIN FROM STREPTOMYCES GRISEUS NONACTINE, FROM STREPTOMYCES SP. NONACTIN FROM STREPTOMYCES TSUSIMAENSIS nonactinfromstreptomycessp. NONACTINE, STREPTOMYCES GRISEUS Nonactin, Amonium Ionophore, Werramycin A, Polynactin Ammonium ionophore, Nonactin (1R,2R,5R,7R,10S,11S,14S,16S,19R,20R,23R,25R,28S,29S,32S,34S)-2,5,11,14,20,23,29,32-Octamethyl-4,13,22,31,37,38,39,40-octaoxapentacyclo[32.2.1.17,10.116,19.125,28]tetracontane-3,12,21,30-tetrone WerraMycin, FH 3582A, NSC 52141, AKD 1A, KD 1A Nonactin / 5342 Pfw 19 / A 4426 / Ammonium ionophore I Nonactin from Streptomyces griseus var griseus AMMONIUM IONOPHORE AMMONIUM IONOPHORE I WERRAMYCIN A -(1r*,2r*,5r*,7r*,10s*,11s*,14s*,16s*,19r*,20r*,23r*,25r*,28s*,29s*,32s*,34s*) 28))tetracontane-3,12,21,30-tetrone,2,5,11,14,20,23,29,32-octamethyl-2(1r 3584-a 4,13,22,31,37,38,39,40-octaoxapentacyclo(32.2.1.1(sup7,10).1(sup16,19).1(sup a-5584 e-79-c fh-3582-a n-329-a 4,13,22,31,37,38,39,40-Octaoxapentacyclo[32.2.1.17,10.116,19.125,28]tetracontane-3,12,21,30-tetrone, 2,5,11,14,20,23,29,32-octamethyl-, (1R,2R,5R,7R,10S,11S,14S,16S,19R,20R,23R,25R,28S,29S,32S,34S)- NONACTIN USP/EP/BP Nonactin (Mixture contains Monactin and Dinactin) (Technical Grade) Nonactin, Monactin, and Dinactin Mixture 6833-84-7 C40H64O12 Antibiotics A to Z Antibiotics N-S Antibiotics Ionophores Potentiometric for ISE Ion Sensor Materials BioChemical Analytical Chromatography Product Catalog inhibitor
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