| Weight | 480.901 g/mol |
|---|---|
| Formula | C22H25ClN2O8 |
| Hydrogen Acceptors | 9 |
| Hydrogen Donors | 6 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
TETRACYCLINE HYDROCHLORIDE (64-75-5)
Tetracycline · Achromycin · Achromycin V
Score:
#309 in Biochemistry
,
#1138 in Biology
,
#1289 in Chemistry
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- Tight control of gene expression in mammalian cells by tetracycline-responsive promoters. (Proceedings of the National Academy of Sciences of the United States of America, 1992)
- Tetracycline Antibiotics: Mode of Action, Applications, Molecular Biology, and Epidemiology of Bacterial Resistance (Microbiology and Molecular Biology Reviews, 2001)
- Release of tetracycline hydrochloride from electrospun poly(ethylene-co-vinylacetate), poly(lactic acid), and a blend. (Journal of Controlled Release, 2002)
- A TETRACYCLINE DERIVATIVE, MINOCYCLINE, REDUCES INFLAMMATION AND PROTECTS AGAINST FOCAL CEREBRAL ISCHEMIA WITH A WIDE THERAPEUTIC WINDOW (Proceedings of the National Academy of Sciences of the United States of America, 1999)
- Tetracycline-based histological analysis of bone remodeling (Calcified Tissue International, 1969)
- Exploring the sequence space for tetracycline-dependent transcriptional activators: Novel mutations yield expanded range and sensitivity (Proceedings of the National Academy of Sciences of the United States of America, 2000)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Tetracycline
- Achromycin
- Achromycin V
- Topicycline
- Tetracycline Monohydrochloride
- Sustamycin
- Hostacyclin
- 4 Epitetracycline
- Tetrabid
- 4-Epitetracycline
-
SMILESCC1(C2CC3C(C(=O)C(=C(C3(C(=O)C2=C(C4=C1C=CC=C4O)O)O)O)C(=O)N)N(C)C)O.Cl
-
InChIKeyYCIHPQHVWDULOY-UHFFFAOYSA-N
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