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Acetomycin

Chemicals & Biochemicals

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Article No

BVT-0150-M001

Size

1 mg

Shipping Information

Article No

BVT-0150-M001

Size

1 mg

Specifications

CAS No	510-18-9
MW	214.2
Article No	BVT-0150-M001
Country Availability	SE, FI, DK, NO, IS, EE, LV, LT
Description	Acetomycin
Supplier	Adipogen Life Sciences
Format	Powder
Notes	Antibiotic. Antibacterial, antifungal and antiprotozoal. Cytotoxic against several tumor cell lines in vitro.\|Chemical. CAS: 510-18-9. Formula: C10H14O5. MW: 214.2. Isolated from Streptomyces ramulosus. Antibiotic. Antibacterial, antifungal and antiprotozoal. Cytotoxic against several tumor cell lines in vitro.
Molecular Formula	C10H14O5
Alias Names	NSC350598; 3-Acetyl-5-(acetyloxy)dihydro-3,4-dimethyl-2(3H)furanone; (2R,3S,4S)-4-Acetyl-3,4-dimethyl-5-oxotetrahydro-furan-2-yl acetate
Product Type	Chemicals & Biochemicals
Purity	>98%
Research area	Immunology
Shipping Information	RT
Size	1 mg
Solubility	Soluble in DMSO or methanol.
Stability	Stable for at least 1 year after receipt when stored at -20°C. After reconstitution protect from light at -20°C.
Storage	-20°C, 4°C
Technical Specifications	Chemical. CAS: 510-18-9. Formula: C10H14O5. MW: 214.2. Isolated from Streptomyces ramulosus. Antibiotic. Antibacterial, antifungal and antiprotozoal. Cytotoxic against several tumor cell lines in vitro.
Product Page Updated	2024-02-01T08:25:01.492Z

Documentation

Datasheet

MSDS

References

The structure of acetomycin. Spectroscopic characterization and X-ray analysis of a bromo derivative: H. Uhr, et al.; J. Antibiot. 38, 1684 (1985) | Biological effects of acetomycin. I. Activity against tumor cells in vitro and in vivo: S.W. Mamber, et al.; J. Antibiot. 40, 73 (1987) | Biological effects of acetomycin. II. Inactivation by esterases in vitro: S.W. Mamber, et al.; J. Antibiot. 40, 77 (1987) | The structure and absolute configuration of acetomycin: F.H. Cano, et al.; Acta Cryst. C. 44, 919 (1988). | Synthesis and in vitro cytotoxicity of acetomycin and related analogs: D. Chen, et al.; Bioorg. Med. Chem. Lett. 5, 759 (1995) | Total synthesis of (±)-acetomycin and design of esterase-resistant analogs: J. Uenishi, et al.; Chem. Pharm. Bull. 47, 517 (1999) | Formation of chiral quaternary carbon stereocenters using silylene transfer reactions: Enantioselective synthesis of (+)-5-epi-acetomycin: S.A. Calad, et al.; Org. Lett. 9, 1037 (2007)

Shipping info

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