CAS 808-26-4
:Sancycline
Description:
Sancycline, with the CAS number 808-26-4, is a synthetic antibiotic belonging to the tetracycline class of compounds. It exhibits broad-spectrum antibacterial activity, making it effective against a variety of Gram-positive and Gram-negative bacteria. Sancycline works by inhibiting bacterial protein synthesis, thereby preventing the growth and reproduction of bacteria. This compound is characterized by its unique chemical structure, which includes a naphthacene ring system, contributing to its pharmacological properties. It is typically administered in a pharmaceutical form, and its solubility and stability can vary depending on the formulation. Sancycline is often used in clinical settings to treat infections, but like other antibiotics, it may be associated with side effects, including gastrointestinal disturbances and potential allergic reactions. Additionally, the emergence of antibiotic resistance is a concern with its use, necessitating careful consideration in prescribing practices. Overall, Sancycline represents an important tool in the fight against bacterial infections, although its use must be managed judiciously to maintain its efficacy.
Formula:C21H22N2O7
InChI:InChI=1S/C21H22N2O7/c1-23(2)15-10-7-9-6-8-4-3-5-11(24)12(8)16(25)13(9)18(27)21(10,30)19(28)14(17(15)26)20(22)29/h3-5,9-10,15,24,26-27,30H,6-7H2,1-2H3,(H2,22,29)/t9-,10-,15-,21-/m0/s1
InChI key:InChIKey=XDVCLKFLRAWGIT-ADOAZJKMSA-N
SMILES:O[C@]12[C@]([C@H](N(C)C)C(O)=C(C(N)=O)C1=O)(C[C@]3(C(=C2O)C(=O)C=4C(C3)=CC=CC4O)[H])[H]
Synonyms:- (2E,4S,4aS,5aR,12aS)-2-[amino(hydroxy)methylidene]-4-(dimethylamino)-10,11,12a-trihydroxy-4a,5a,6,12a-tetrahydrotetracene-1,3,12(2H,4H,5H)-trione
- (2Z,4S,4aS,5aR,12aS)-2-[amino(hydroxy)methylidene]-4-(dimethylamino)-10,11,12a-trihydroxy-4a,5a,6,12a-tetrahydrotetracene-1,3,12(2H,4H,5H)-trione
- (4S,4aS,5aR,12aS)-4-(Dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,10,12,12a-tetrahydroxy-1,11-dioxo-2-naphthacenecarboxamide
- 2-Naphthacenecarboxamide, 4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,10,12,12a-tetrahydroxy-1,11-dioxo-, (4S,4aS,5aR,12aS)-
- 2-Naphthacenecarboxamide, 4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,10,12,12a-tetrahydroxy-1,11-dioxo-, [4S-(4α,4aα,5aα,12aα)]-
- 4-(Dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,10,12,12a-tetrahydroxy-1,11-dioxo-2-naphthacenecarboxamide
- 6-Demethyl-6-deoxytetracycline
- Bonomycin
- Gs 2147
- Norcycline
- Sancyclin
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Found 9 products.
Minocycline EP Impurity B (Sancycline)
CAS:Formula:C21H22N2O7Color and Shape:Off-White SolidMolecular weight:414.41Sancycline
CAS:Sancycline is a semisynthetic tetracycline that inhibits protein translation.Cost-effective and quality-assured.Formula:C21H22N2O7Purity:98.41% - 99.83%Color and Shape:SolidMolecular weight:414.41Sancycline
CAS:<p>Sancycline is an amide tetracycline antibiotic. This drug binds to the 30S ribosomal subunit and inhibits protein synthesis, which leads to bacterial cell death. Sancycline is effective against a wide range of bacteria that cause infectious diseases, such as streptococci, pneumococci, staphylococci, and gonococci. The structure of this drug was determined by X-ray crystallography. The photochemical properties of sancycline were also studied in tissue culture cells. It has been shown that sancycline binds to the nuclear DNA of cells and prevents DNA synthesis by inhibiting the binding of aminoacyl-tRNA to diazonium salt-treated nuclei. Sancycline also reacts with hydrogen molecules in the reaction solution to form reactive intermediates that can react with alkylsulfonyl groups on proteins or DNA.</p>Formula:C21H22N2O7Purity:Min. 95%Molecular weight:414.41 g/mol
