Rutamycin

Product Code:

TAR-T28626

Product Group:

Inhibitors and Activators

Supplier:

TargetMol

Regulatory Status:

RUO

Shipping:

cool pack

Storage:

-20℃

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Code	Size	Price

TAR-T28626-5mg

5mg

£2,000.00

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Quantity:

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Further Information

Bioactivity:

Rutamycin is a macrolide antibiotic of the oligomycin group obtained from Streptomyces rutgersensis. It inhibits various ATPases and uncouples oxidative phosphorylation from electron transport.

CAS:

1404-59-7

Formula:

C44H72O11

Molecular Weight:

777.049

Purity:

0.98

SMILES:

CC[C@@H]1CC[C@@H]2O[C@]3(CC[C@H](C)[C@H](C[C@@H](C)O)O3)C[C@H](OC(=O)C=C[C@H](C)[C@@H](O)[C@H](C)C(=O)[C@H](C)[C@@H](O)[C@H](C)C(=O)[C@](C)(O)[C@@H](O)[C@H](C)CC=CC=C1)[C@@H]2C

Documents

References

1. Lichtor T, Getz GS. Cytoplasmic inheritance of rutamycin resistance in mouse fibroblasts. Proc Natl Acad Sci U S A. 1978 Jan;75(1):324-8. PubMed PMID: 146879; PubMed Central PMCID: PMC411240. 2. Panek JS, Jain NF. Total synthesis of rutamycin B and oligomycin C. J Org Chem. 2001 Apr 20;66(8):2747-56. PubMed PMID: 11304197. 3. Foury F, Tzagoloff A. Localization on mitochondrial DNA of mutations leading to a loss of rutamycin-sensitive adenosine triphosphatase. Eur J Biochem. 1976 Sep;68(1):113-9. PubMed PMID: 134892. 4. White JD, Hanselmann R, Jackson RW, Porter WJ, Ohba Y, Tiller T, Wang S. Total synthesis of rutamycin B, a macrolide antibiotic from Streptomyces aureofaciens. J Org Chem. 2001 Jul 27;66(15):5217-31. PubMed PMID: 11463276.