1. Anti-infection
  2. Bacterial
  3. Mycobacterium tuberculosis-IN-9

Mycobacterium tuberculosis-IN-9 is an orally active Mycobacterium tuberculosis BioA inhibitor with a Ki value of 0.2 nM. Mycobacterium tuberculosis-IN-9 targets the biotin biosynthesis pathway. Mycobacterium tuberculosis-IN-9 inhibits the growth of Mycobacterium tuberculosis in mouse models and is effective against both drug-sensitive and drug-resistant strains. Mycobacterium tuberculosis-IN-9 can be used for the research of tuberculosis.

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

Mycobacterium tuberculosis-IN-9

Mycobacterium tuberculosis-IN-9 Chemical Structure

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Description

Mycobacterium tuberculosis-IN-9 is an orally active Mycobacterium tuberculosis BioA inhibitor with a Ki value of 0.2 nM. Mycobacterium tuberculosis-IN-9 targets the biotin biosynthesis pathway. Mycobacterium tuberculosis-IN-9 inhibits the growth of Mycobacterium tuberculosis in mouse models and is effective against both drug-sensitive and drug-resistant strains. Mycobacterium tuberculosis-IN-9 can be used for the research of tuberculosis[1].

In Vitro

Mycobacterium tuberculosis-IN-9 (compound c48) potently inhibits purified Mycobacterium tuberculosis BioA enzyme with a Ki of 0.2 nM[1].
Mycobacterium tuberculosis-IN-9 inhibits the growth of wild-type Mycobacterium tuberculosis H37Rv in biotin-free medium with an MIC50 of 0.093 μM, while it shows no inhibition in medium supplemented with 2 μM biotin and has an MIC50 greater than 100 μM[1].
Mycobacterium tuberculosis-IN-9 inhibits the growth of Mycobacterium tuberculosis BioA-underexpressed strain with an MIC50 of 0.014 μM[1].
Mycobacterium tuberculosis-IN-9 inhibits the growth of Mycobacterium tuberculosis BioA-overexpressed strain with an MIC50 of 0.37 μM[1].
Mycobacterium tuberculosis-IN-9 inhibits the growth of a panel of drug-sensitive and drug-resistant Mycobacterium tuberculosis isolates with MICs ranging from 0.012 to 0.093 μM[1].
Mycobacterium tuberculosis-IN-9 (0.3-30 μM; 5 min (each concentration applied twice)) weakly inhibits hERG channels in HEK-293 cells[1].
Mycobacterium tuberculosis-IN-9 (Up to 100 μM) is not cytotoxic to HepG2 human liver cancer cells, with an IC50 greater than 100 μM[1].

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

Parmacokinetics
Species Dose Route AUC0-∞ F Vd CL T1/2
Mice[1] 5 mg/kg i.v. 3.3 μg·h/mL / 0.26 L/kg 3.2 mL/min/kg 0.91 h
Mice[1] 25 mg/kg p.o. 146 μg·h/mL >100 % / / /
Molecular Weight

418.26

Formula

C19H17BrFN3O2

SMILES

O=C(N1CCN(C2=NC=C3C(CCC3=C2)=O)CC1)C4=CC(Br)=C(C=C4)F

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
References
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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Product Name:
Mycobacterium tuberculosis-IN-9
Cat. No.:
HY-183606
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