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Cat.No.S4156
| Related Targets | Integrase Bacterial Antibiotics Anti-infection Fungal Antiviral COVID-19 Parasite Reverse Transcriptase HIV |
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| Other Antineoplastic and Immunosuppressive Antibiotics Inhibitors | Staurosporine (STS) Cyclosporin A Puromycin Dihydrochloride Oligomycin A (MCH 32) Geldanamycin Honokiol Streptozotocin (STZ) Cephalomannine Sodium Monensin (NSC 343257) 10-Deacetylbaccatin-III |
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In vitro |
DMSO
: 10 mg/mL
(19.4 mM)
Water : 2 mg/mL Ethanol : Insoluble |
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In vivo |
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Step 1: Enter information below (Recommended: An additional animal making an allowance for loss during the experiment)
Step 2: Enter the in vivo formulation (This is only the calculator, not formulation. Please contact us first if there is no in vivo formulation at the solubility Section.)
Calculation results:
Working concentration: mg/ml;
Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )
Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.
Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.
Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such
as vortex, ultrasound or hot water bath can be used to aid dissolving.
| Molecular Weight | 515.34 | Formula | C22H23ClN2O8.HCl |
Storage (From the date of receipt) | |
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| CAS No. | 64-72-2 | Download SDF | Storage of Stock Solutions |
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| Synonyms | 7-Chlorotetracycline HCl, Aureomycin monohydrochloride | Smiles | CC1(C2CC3C(C(=O)C(=C(C3(C(=O)C2=C(C4=C(C=CC(=C41)Cl)O)O)O)O)C(=O)N)N(C)C)O.Cl | ||
| In vitro |
Chlortetracycline HCl (NSC 13252), obtained from Streptomyces aureofaciens, is a broad-spectrum antibacterial agent with activity against a wide range of Gram-positive and Gram-negative bacteria, including obligate anaerobes. It binds strongly to a single site on the 30S subunit and inhibits bacterial growth primarily by inhibiting protein synthesis at the level of the ribosome. This compound is active against Streptococcus pyogelles, Diplococcus pneuliloniap, Bacillus subtilis, Streptococcus faecalis, Bacillus subtilis, Mycobacterium ranae with MIC of 0.292, 0.098, 0.195, 0.3, 0.15, 0.3 mg/L.
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References |
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