[CAS NO. 18323-44-9]  Clindamycin

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PRODUCTS SPECIFICATIONS [18323-44-9]

Catalog
HY-B1455
Brand
MCE
CAS
18323-44-9

DESCRIPTION [18323-44-9]

Overview

MDL-
Molecular Weight424.98
Molecular FormulaC18H33ClN2O5S
SMILESCN(C[C@H](CCC)C1)[C@@H]1C(N[C@@]([C@@H](Cl)C)([H])[C@@]2([H])O[C@H](SC)[C@H](O)[C@@H](O)[C@H]2O)=O

For research use only. We do not sell to patients.


Summary

Clindamycin is an orally active and broad-spectrum bacteriostatic lincosamide antibiotic . Clindamycin can inhibit bacterial protein synthesis , possessing the ability to suppress the expression of virulence factors in Staphylococcus aureus at sub-inhibitory concentrations (sub-MICs). Clindamycin resistance results from enzymatic methylation of the antibiotic binding site in the 50S ribosomal subunit (23S rRNA). Clindamycin decreases the production of Panton-Valentine leucocidin (PVL), toxic-shock-staphylococcal toxin (TSST-1) or alpha-haemolysin (Hla). Clindamycin also can be used for researching malaria [1] [2] .


IC50 & Target

Plasmodium


In Vitro

Clindamycin (25 μg/mL, 1-18 h) inhibits ceftazidime ( HY-B0593 )-induced endotoxin release pretreatment in E. coli O55:B5 [3] .
Clindamycin (50-100 μg/mL, 0-12 min) enhances antibody- and complement-dependent phagocytosis in Staphylococcus aureus [4] .
Clindamycin (0-500 μg/mL, 24-72 h) inhibits the cell proliferation in osteoblast cell culture model, stimulates the cell metabolism of osteoblast at the contratibution of 10 μg/mL [5] .

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Viability Assay [3]

Cell Line: THP-1 cells with stimulated E. coli O55:B5
Concentration: 3.13-50 μg/mL
Incubation Time: 1-18 h
Result: Reduced TNF-α concentrations after pretreatment for 4 or 18 h at 25 and 50 μg/mL.

Cell Viability Assay [5]

Cell Line: Osteoblast cell culture model
Concentration: 0-500 μg/mL
Incubation Time: 24-72 h
Result: Increased alkaline phosphatase (ALP)-activity at 10 μg/mL at 24 and 48 h.
Increased LDH values at 500 μg/mL at 24 and 48 h, indicating cytotoxicity.
Increased calcification at 10 and 25 μg/mL,decreased or no calcification was found at 50 μg/ml.

In Vivo

Clindamycin (50-300 mg/kg; i.v., p.o.) dosage doesn’t affect pharmacokinetic parameters in rats [6] .
Clindamycin (160-600 mg/kg; i.v.) improves survival in a dose-dependent manner in endotoxic shock mouse model [7] .
Clindamycin (17-50 mg/kg, i.v.) has good penetration into rat muscle tissue that can be applied to inhibit the main bacteria causing odontogenic infections [8] .

1.19
Pharmacokinetic Analysis in Rat Model [8]
Route Dose (mg/kg) t 1/2 (h) C max (mg/mL) T max (h)a AUC 0-inf (h.mg/L) ∱T
i.v. 51(Plasma) 2.51 (2.37–2.83) 35.21 (25.04–42.65) 0.08 ± 0.00 44.78 (28.82–65.65) /
i.v. 51(Tissue) 2.82 (2.57–3.05) 14.20 (10.63–14.89) 0.25 ± 0.00 16.54 (13.83–18.35) 1.10
i.v. 17(Tissue) 3.25 (3.13–3.44) 4.82 (3.35–6.66 0.25 ± 0.00 / /

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Endotoxic shock mouse model [7]
Dosage: 160-600 mg/kg
Administration: Intravenous injection (i.v.)
Result: Decreased survival rates to 92 and 36% treated with 520- and 600-mg/kg doses.
Lowered the peak concentrations of tumor necrosis factor alpha (TNF-α) and interleukin-1β (IL-1β) in serum.
Increased the the peak concentrations of IL-6 in the sera.

Clinical Trial

NCT Number Sponsor Condition Start Date Phase
NCT03412071 University of Toronto|UVRI-IAVI HIV Vaccine Program|Entebbe General Hospital
Foreskin HIV Susceptibility
December 7, 2017 Not Applicable
NCT00689117 Stiefel, a GSK Company|GlaxoSmithKline
Acne Vulgaris|Acne
April 2008 Phase 3
NCT02515305 Padagis LLC
Acne
July 2015 Phase 3

Appearance

Solid


Shipping

Room temperature in continental US; may vary elsewhere.


Storage

-20°C, protect from light

* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)


Solvent & Solubility

In Vitro:

DMSO : 125 mg/mL ( 294.13 mM ; Need ultrasonic)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 2.3531 mL 11.7653 mL 23.5305 mL
5 mM 0.4706 mL 2.3531 mL 4.7061 mL
10 mM 0.2353 mL 1.1765 mL 2.3531 mL
* Please refer to the solubility information to select the appropriate solvent.