Actaplanins
Structural Formula Vector Image
Title: Actaplanins
Manufacturers' Codes: A-4696
Trademarks: Kamoran (Lilly)
Literature References: Complex of glycopeptide antibiotics produced by Actinoplanes missouriensis. Six actaplanins (A, B1, B2, B3, C1, G) have been isolated and characterized as having a central peptide core with the amino sugar ristosamine and up to four neutral sugars attached. Isoln: R. L. Hamill et al., DE 2209018 (1972 to Lilly), C.A. 77, 138338n (1972); A. P. Raun, US 3816618; R. L. Hamill et al., US 4115552 (1974, 1978 to Lilly). Chemical characterization: M. Debono et al., J. Antibiot. 37, 85 (1984). 1H NMR studies and structures: A. H. Hunt et al., J. Org. Chem. 49, 635 (1984); eidem, ibid. 641. Growth promotant activity: C. Tsaltos et al., Bull. Hellenic Vet. Med. Soc. 33, 139 (1982). Use to increase milk production in ruminants: C. C. Scheifinger, EP 63491; idem, US 4430328 (1982, 1984 to Eli Lilly). Determn in milk: K. H. Hahne et al., Milchwissenschaft 39, 473 (1984).
 
Derivative Type: Hydrochloride
Properties: White cryst solid, mp >220°. Approx mol wt 1158. [a]D25 -42.3° (c = 1 in water). uv max (acidic and neutral solns): 276 nm (E1%1 cm 65). Sol in water. Insol in most organic solvents. Stable over pH 1.0 to 10.0 up to 27°.
Melting point: mp >220°
Optical Rotation: [a]D25 -42.3° (c = 1 in water)
Absorption maximum: uv max (acidic and neutral solns): 276 nm (E1%1 cm 65)
 
Therap-Cat-Vet: Growth stimulant.

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