Pfizer Handbook of Microbial Metabolites 



36 



A. Angeletti, G. Tappi and G. Biglino, Ann. chim. (Rome) 

 42 502 (1952). 



50 d-2-Octadecanol, CigHgsO, colorless needles, m.p. 56°, [ctjo +5.7° 



(in chloroform). 



CHslCHalisCHCHa 



I 

 OH 



Mycobacterium tuberculosis var. hominis, M. avium, 

 M. phlei 



Mary C. Panghorn and R. J. Anderson, /. Am. Chem. Soc. 

 58 10 (1936). 



R. E. Reeves and R. J. Anderson, ibid. 59 858 (1937). 



R. J. Anderson, J. A. Crowder, M. S. Newman and F. H. 

 Stodola, J. Biol. Chem. 113 637 (1936). 



51 d-3-Octadecanol, CisHggO, colorless crystals, m.p. 56°. 



CH3(CH2),4CHCH2CH3 



OH 



Corynebacterium diphtheriae 



A. A. Kanchukh, Ukrain. Biokhim. Zhur. 26 186 (1954). 



52 Kanamycin, C18H36O11N4, Sulfate: white prisms which decom- 



pose over a wide range above 250°, [ajn"* +146° (c 1 in 

 0.1 N sulfuric acid). 



CH2NH 



6-Glucosamine< 



Kanosamine 



>2-Deoxystrep- 

 tamine 



Streytomyces kanainyceticus 



Tomio Takeuchi, Tokuro Hikiji, Kazuo Nitta, Seiro Yama- 

 zaki, Sadao Abe, Hisaro Takayama and Hamao Umezawa, /. 

 Antibiotics (Japan) lOA 107 (1957). 



Hamao Umezawa, Mashiro Ueda, Kenji Maeda, Koki 



