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Rutamycin, also known as Oligomycin D, is a macrolide antibiotic derived from various species of Streptomyces. It is a macrocyclic lactone belonging to the oligomycin class and was first identified in 1961. Rutamycin inhibits mitochondrial F1F0-ATPase, making it a significant bioprobe for studying the organization of ATPase on the mitochondrial membrane. It exhibits a broad biological profile, including antifungal, antitumor, and nematocidal activities.

1404-59-7

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1404-59-7 Usage

Uses

Used in Pharmaceutical Industry:
Rutamycin is used as an inhibitor of mitochondrial F1F0-ATPase for its cytotoxic effects on certain cancer cells, such as SW620 colon cancer cells, with an IC50 value of 36 μM. It also inhibits K-Ras plasma membrane localization in MDCK cells with an IC50 value of 3.49 nM.
Used in Research Applications:
Rutamycin is used as a bioprobe to study the organization of ATPase on the mitochondrial membrane, which is crucial for understanding the mechanisms of oxidative phosphorylation and electron transport.
Used in Antifungal Applications:
Rutamycin exhibits antifungal properties, making it useful in the treatment and prevention of fungal infections.
Used in Anthelmintic Applications:
Due to its nematocidal activities, Rutamycin can be employed in the treatment of nematode infections.

Check Digit Verification of cas no

The CAS Registry Mumber 1404-59-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,0 and 4 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1404-59:
(6*1)+(5*4)+(4*0)+(3*4)+(2*5)+(1*9)=57
57 % 10 = 7
So 1404-59-7 is a valid CAS Registry Number.
InChI:InChI=1/C44H72O11/c1-11-33-16-14-12-13-15-27(4)41(50)43(10,52)42(51)32(9)40(49)31(8)39(48)30(7)38(47)26(3)17-20-37(46)53-36-24-44(54-34(19-18-33)29(36)6)22-21-25(2)35(55-44)23-28(5)45/h12-14,16-17,20,25-36,38,40-41,45,47,49-50,52H,11,15,18-19,21-24H2,1-10H3/b13-12-,16-14+,20-17+/t25-,26-,27+,28+,29+,30-,31-,32-,33-,34-,35-,36-,38+,40+,41-,43+,44-/m1/s1

1404-59-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (1R,4S,5E,5'R,6'R,7E,10S,11R,12S,14R,15S,16S,18R,19S,20R,21E,25R,27S,29S)-4-ethyl-11,12,15,19-tetrahydroxy-6'-[(2S)-2-hydroxypropyl]-5',10,12,14,16,18,20,29-octamethylspiro[24,28-dioxabicyclo[23.3.1]nonacosa-5,7,21-triene-27,2'-oxane]-13,17,23-trione

1.2 Other means of identification

Product number -
Other names Rutamycine [INN-French]

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1404-59-7 SDS

1404-59-7Upstream product

1404-59-7Downstream Products

1404-59-7Related news

Synthesis of the C(3)C(15) segment of Rutamycin (cas 1404-59-7) B via a C(8)C(9) fragment assembly aldol reaction: Metal dependence of the aldehyde and enolate diastereofacial selectivities09/08/2019

The diastereofacial selectivities of aldehyde 2b and ketone 3 are metal dependent, and their fragment assembly aldol coupling is a matched double asymmetric reaction when a chlorotitanium enolate is used.detailed

Cytoplasmic inheritance of oligomycin and Rutamycin (cas 1404-59-7) resistance in yeast☆09/05/2019

Oligomycin resistant yeast mutants induced by ultraviolet irradiation were also resistant to rutamycin and/or venturicidin. One of the two mutants analyzed in detail showed cytoplasmic inheritance of oligomycin and rutamycin resistance while in the other strain, inheritance of oligomycin and ven...detailed

Application of chiral (E)-crotylsilanes in synthesis: The asymmetric synthesis of the C19C34 spiroketal fragment of Rutamycin (cas 1404-59-7) B09/04/2019

The asymmetric synthesis of the spiroketal fragment of rutamycin B is reported employing allylsilane bond construction methodology for the introduction of five of the eight stereogenic centers. In this paper, the construction of the C19C28 and C29C34 fragments as well as their coupling throu...detailed

Application of chiral (E)-crotylsilanes in synthesis: The asymmetric synthesis of the C1C17 polypropionate fragment of Rutamycin (cas 1404-59-7) B09/03/2019

The asymmetric synthesis of the polypropionate fragment of rutamycin B is reported employing chiral allylsilane bond construction methodology for the introduction of six of the nine stereogenic centers. In this paper, the construction of the C3C12 subunit and its coupling to the aldehyde 12 th...detailed

Studies directed toward the synthesis of the Rutamycin (cas 1404-59-7)s. Assemblage of the polypropionate region of Rutamycin (cas 1404-59-7) B09/01/2019

the asymmetric synthesis of the polypropionate segment of rutamycin B is reported. In this convergent synthesis the construction of the C1-C8 and C9-C17 subunits and their union through a double stereodifferentiating aldol fragment coupling are described. The stereoselectivity of this coupling r...detailed

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