Clindamycin 2-phosphate
aminoglycoside antibiotic
Manufacturer: Sigma Aldrich
CAS Number: 24729-96-2
Synonym(S): Clindamycin 2-dihydrogen phosphate
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 50 MG | C6427-50-MG | In Stock | ₹ 14,851.90 |
| 100 MG | C6427-100-MG | In Stock | ₹ 25,601.13 |
C6427 - 50 MG
In Stock
Quantity
1
Base Price: ₹ 14,851.90
GST (18%): ₹ 2,673.342
Total Price: ₹ 17,525.242
Quality Level
100
form
solid
solubility
DMSO: 224 mg/mL at 25 °C
antibiotic activity spectrum
Gram-positive bacteria
Mode of action
protein synthesis | interferes
storage temp.
2-8°C
SMILES string
CCC[C@@H]1C[C@H](N(C)C1)C(=O)NC([C@H](C)Cl)C2O[C@H](SC)[C@H](OP(O)(O)=O)[C@@H](O)[C@H]2O
InChI
1S/C18H34ClN2O8PS/c1-5-6-10-7-11(21(3)8-10)17(24)20-12(9(2)19)15-13(22)14(23)16(18(28-15)31-4)29-30(25,26)27/h9-16,18,22-23H,5-8H2,1-4H3,(H,20,24)(H2,25,26,27)/t9-,10+,11-,12?,13+,14-,15?,16+,18+/m0/s1
InChI key
UFUVLHLTWXBHGZ-MWBQRTRKSA-N
Other Options
| Image | Product Name | Manufacturer | Price Range | |
|---|---|---|---|---|
 | Clindamycin Phosphate | Supelco | ₹ 11,506.98 | |
| | Clindamycin phosphate | Sigma Aldrich | ₹ 16,107.60 | |
| | Clindamycin phosphate for system suitability | Sigma Aldrich | ₹ 16,107.60 |
Related Products
Description
- General description: Chemical structure: macrolide
- Application: Clindamycin 2-phosphate is an aminoglycoside antibiotic that has been used to study the cytoxicity of antibiotics on human cell lines [1], Bacterial protein synthesis and peptide translation, and the inhibition of human Tyrosyl-DNA Phosphodiesterase [2].
- Biochem/physiol Actions: Clindamycin 2-phosphate is a pharmacological tyrosyl-DNA phosphodiesterase (Tdp1) inhibitor. Clindamycin 2-phosphate can repair DNA topoisomerase I-DNA covalent complexes by hydrolyzing the tyrosyl-DNA bond. It inhibits protein synthesis in bacteria by binding the 50s ribosomal subunit. [2]. Spectrum of Activity: Gram positive cocci and taxoplasma. Especially active against anaerobic bacteria.
- Other Notes: Antibacterial and antiprotozoal antibiotic of the licosamide class.
SAFETY INFORMATION
Pictograms
Signal Word
Warning
Hazard Statements
Precautionary Statements
P260 - P263 - P280 - P301 + P312 - P302 + P352 - P308 + P313
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Lact. - Skin Sens. 1
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Compare Similar Items
Show Difference
Quality Level: 100
form: solid
solubility: DMSO: 224 mg/mL at 25 °C
antibiotic activity spectrum: Gram-positive bacteria
Mode of action: protein synthesis | interferes
storage temp.: 2-8°C
SMILES string: CCC[C@@H]1C[C@H](N(C)C1)C(=O)NC([C@H](C)Cl)C2O[C@H](SC)[C@H](OP(O)(O)=O)[C@@H](O)[C@H]2O
InChI: 1S/C18H34ClN2O8PS/c1-5-6-10-7-11(21(3)8-10)17(24)20-12(9(2)19)15-13(22)14(23)16(18(28-15)31-4)29-30(25,26)27/h9-16,18,22-23H,5-8H2,1-4H3,(H,20,24)(H2,25,26,27)/t9-,10+,11-,12?,13+,14-,15?,16+,18+/m0/s1
InChI key: UFUVLHLTWXBHGZ-MWBQRTRKSA-N
Quality Level: __
form: __
solubility: __
antibiotic activity spectrum: __
Mode of action: __
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SMILES string: __
InChI: __
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Quality Level: 100
form: solid
solubility: __
antibiotic activity spectrum: __
Mode of action: __
storage temp.: room temp
SMILES string: NC(Cc1ccc(Cl)cc1)C(O)=O
InChI: 1S/C9H10ClNO2/c10-7-3-1-6(2-4-7)5-8(11)9(12)13/h1-4,8H,5,11H2,(H,12,13)
InChI key: __