C6427

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

₹ 14,851.90

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
50-249-1454
eMolecules​ Medchem Express / Clindamycin phosphate / 100mg / 415688860 / HY-B1064 / / 24729-96-2 / MFCD11982855 / 504.960 / C18H34ClN2O8PS
eMolecules​ ₹ 7,556.66
NC1443203
U.S. Pharmacopeia Clindamycin Phosphate System Suitability | 24729-96-2 | MFCD11982855 | 30 mg
U.S. Pharmacopeia ₹ 51,336.00
PHR1021
Clindamycin Phosphate
Supelco ₹ 11,506.98
C2269000
Clindamycin phosphate
Sigma Aldrich ₹ 16,107.60
Y0001680
Clindamycin phosphate for system suitability
Sigma Aldrich ₹ 16,107.60
CS-4620
Clindamycin phosphate
ChemScene ₹ 5,133.60
AB72190
24729-96-2 | Clindamycin Phosphate
A2B Chem ₹ 855.60 - ₹ 40,983.24

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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

GHS07

Signal Word

Warning

Hazard Statements

H302,H317,H319,H362

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

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Quality Level:
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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

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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

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