| Weight | 581.58 g/mol |
|---|---|
| Formula | C21H39N7O12 |
| Hydrogen Acceptors | 15 |
| Hydrogen Donors | 12 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 9 |
Streptomycin sulfate (3810-74-0)
Streptomycin · Streptomycin Sulphate · Estreptomicina Normon
Score:
#485 in Microbiology
,
#3833 in Biology
,
#4825 in Chemistry
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- TCI - Streptomycin sulfate24.00 - 227.00 USD
- Use of acid, rose bengal, and streptomycin in the plate method for estimating soil fungi. (Soil Science, 1950)
- Streptomycin, a Substance Exhibiting Antibiotic Activity Against Gram-Positive and Gram-Negative Bacteria. (Experimental Biology and Medicine, 1944)
- Pretreatment of Mice with Streptomycin Provides a Salmonella enterica Serovar Typhimurium Colitis Model That Allows Analysis of Both Pathogen and Host (Infection and Immunity, 2003)
- Streptomycin treatment of pulmonary tuberculosis. (Medical times, 1949)
- Genome Sequence of the Streptomycin-Producing Microorganism Streptomyces griseus IFO 13350 (Journal of Bacteriology, 2008)
- Streptomycin-resistant plants from callus culture of haploid tobacco. (Nature, 1973)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Streptomycin
- Streptomycin Sulphate
- Estreptomicina Normon
- Strepto Hefa
- Estreptomicina CEPA
- Strepto-Hefa
- Streptomycin Sulfate (2:3) Salt
- Estreptomicina Clariana
- Streptomycine Panpharma
- Strepto Fatol
- Streptomycin Grnenthal
- Strepto-Fatol
-
SMILESCC1C(C(C(O1)OC2C(C(C(C(C2O)O)N=C(N)N)O)N=C(N)N)OC3C(C(C(C(O3)CO)O)O)NC)(C=O)O
-
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