Dianemycin
Names
Biological Activity
[Description]:
Dianemycin (Nanchangmycin free base), produced by Streptomyces nanchangensis NS3226, inhibits gram-positive bacteria[1]. Dianemycin is a broad spectrum antiviral active against Zika virus[2].
[Related Catalog]:
[Target]
Bacteria[1] Zika virus[2]
[In Vitro]
Dianemycin (Nanchangmycin) can be used as a growth promotant in poultry and to cure coccidiosis in chickens. Dianemycin is active against drug resistant strains of malaria[1]. Dianemycin (Nanchangmycin) as a potent inhibitor of Zika virus (ZIKV) entry across all cell types tested including physiologically relevant primary cells. Dianemycin potently reduces infection of all three strains of ZIKV across all three cell types. The IC50s for infection are between 0.1 and 0.4 μM while Dianemycin has low toxicity in these ranges. In addition, DENV is inhibited by Dianemycin across cell types[2].
[References]
Chemical & Physical Properties
[ Density]:
1.21g/cm3
[ Boiling Point ]:
910.3ºC at 760mmHg
[ Molecular Formula ]:
C47H78O14
[ Molecular Weight ]:
867.11
[ Flash Point ]:
256.4ºC
[ Exact Mass ]:
866.53900
[ PSA ]:
188.90000
[ LogP ]:
6.14960
[ Index of Refraction ]:
1.549
Toxicological Information
CHEMICAL IDENTIFICATION
- RTECS NUMBER :
- HL5521000
- CHEMICAL NAME :
- Dianemycin
- CAS REGISTRY NUMBER :
- 35865-33-9
- LAST UPDATED :
- 199612
- DATA ITEMS CITED :
- 3
- MOLECULAR FORMULA :
- C47-H78-O14
- MOLECULAR WEIGHT :
- 867.25
- WISWESSER LINE NOTATION :
- T6OXTJ DQ E1 FY1&1UY1&VY1&1Y1&VQ B-& BT5OXTJ E1 E- ET6OXTJ C1 DO- FT6OTJ B1 CO1& B-& BT5OXTJ
HEALTH HAZARD DATA
ACUTE TOXICITY DATA
- TYPE OF TEST :
- LD50 - Lethal dose, 50 percent kill
- ROUTE OF EXPOSURE :
- Oral
- SPECIES OBSERVED :
- Rodent - mouse
- DOSE/DURATION :
- 150 mg/kg
- TOXIC EFFECTS :
- Details of toxic effects not reported other than lethal dose value
- REFERENCE :
- 37ASAA "Kirk-Othmer Encyclopedia of Chemical Technology," 3rd ed., Grayson, M., and D. Eckroth, eds., New York, John Wiley & Sons, Inc., 1978 Volume(issue)/page/year: 3,47,1978
- TYPE OF TEST :
- LD50 - Lethal dose, 50 percent kill
- ROUTE OF EXPOSURE :
- Intraperitoneal
- SPECIES OBSERVED :
- Rodent - mouse
- DOSE/DURATION :
- 9 mg/kg
- TOXIC EFFECTS :
- Details of toxic effects not reported other than lethal dose value
- REFERENCE :
- 37ASAA "Kirk-Othmer Encyclopedia of Chemical Technology," 3rd ed., Grayson, M., and D. Eckroth, eds., New York, John Wiley & Sons, Inc., 1978 Volume(issue)/page/year: 3,47,1978
- TYPE OF TEST :
- LD50 - Lethal dose, 50 percent kill
- ROUTE OF EXPOSURE :
- Subcutaneous
- SPECIES OBSERVED :
- Rodent - mouse
- DOSE/DURATION :
- 40 mg/kg
- TOXIC EFFECTS :
- Details of toxic effects not reported other than lethal dose value
- REFERENCE :
- JANTAJ Journal of Antibiotics. (Japan Antibiotics Research Assoc., 2-20-8 Kamiosaki, Shinagawa-ku, Tokyo, 141, Japan) V.2-5, 1948-52; V.21- 1968- Volume(issue)/page/year: 22,161,1969
Related Compounds
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