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  3. Delamanid

Delamanid, a newer mycobacterial cell wall synthesis inhibitor, inhibits the synthesisi of mucolic acids.

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

CAS No. : 681492-22-8

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Solid + Solvent (Highly Recommended)
10 mM * 1 mL in DMSO
ready for reconstitution
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Customer Review

Based on 8 publication(s) in Google Scholar

Other Forms of Delamanid:

Top Publications Citing Use of Products

    Delamanid purchased from MedChemExpress. Usage Cited in: Drug Dev Ind Pharm. 2025 Jul 24:1-16.  [Abstract]

    Effect of pure Delamanid (0-10μg/mL) and selected delamanid-loaded microemulsion formulation on cell viability of a549 (a),ncI-h358 (B) cell line using mtt assay treated with various concentrations after 24 h.

    Delamanid purchased from MedChemExpress. Usage Cited in: Drug Dev Ind Pharm. 2025 Jul 24:1-16.  [Abstract]

    Delamanid (0.125, 0.25, 0.5, 1, 2 μg/mL;24 h) showed no effect in levels of inflammatory cytokines;Il-1β (a), Il-6 (B) produced after expo-sure to nr8383 cells.

    Delamanid purchased from MedChemExpress. Usage Cited in: Drug Dev Ind Pharm. 2025 Jul 24:1-16.  [Abstract]

    Delamanid (0.125, 0.25, 0.5, 1, 2 μg/mL;24 h) showed no effect in lnitric oxide (NO) concentration to nr8383 cells.

    Delamanid purchased from MedChemExpress. Usage Cited in: Drug Dev Ind Pharm. 2025 Jul 24:1-16.  [Abstract]

    The viability was compared among M. bovis samples treated with Delamanid (0.156, 0.313, 0.625, 1.25, 2.5, 5 μg/mL) at varying concentrations.

    Delamanid purchased from MedChemExpress. Usage Cited in: Dis Model Mech. 2021 Dec 1;14(12):dmm049145.  [Abstract]

    Delamanid (10 μM) resulted in a significant reduction of the bacterial signal in M. marinum-tdTomato yolk-infected zebrafish embryos.
    • Biological Activity

    • Purity & Documentation

    • References

    • Customer Review

    Description

    Delamanid, a newer mycobacterial cell wall synthesis inhibitor, inhibits the synthesisi of mucolic acids[1].

    Cellular Effect
    Cell Line Type Value Description References
    HepG2 CC50
    107.5 μg/mL
    Compound: Delamanid
    Cytotoxicity against human HepG2 cells after 24 hrs by MTT assay
    Cytotoxicity against human HepG2 cells after 24 hrs by MTT assay
    [PMID: 26487912]
    MRC5 IC50
    0.43 μM
    Compound: 5; OPC-67683
    Antitrypanosomal activity against Trypanosoma cruzi infected in human MRC5 cells assessed as parasite growth inhibition incubated for 7 days by chlorophenol red alpha-D-galactopyranoside-based assay
    Antitrypanosomal activity against Trypanosoma cruzi infected in human MRC5 cells assessed as parasite growth inhibition incubated for 7 days by chlorophenol red alpha-D-galactopyranoside-based assay
    [PMID: 26901446]
    MRC5 IC50
    > 64 μM
    Compound: 5; OPC-67683
    Cytotoxicity against human MRC5 cells assessed as cell viability incubated for 72 hrs by fluorimetric assay
    Cytotoxicity against human MRC5 cells assessed as cell viability incubated for 72 hrs by fluorimetric assay
    [PMID: 26901446]
    Vero CC50
    > 32 μg/mL
    Compound: Delamanid
    Cytotoxicity against African green monkey vero cells assessed as reduction in cell viability
    Cytotoxicity against African green monkey vero cells assessed as reduction in cell viability
    [PMID: 35777718]
    In Vitro

    Delamanid inhibits the synthesisi of mucolic acids, cruciala component of the cell wall of the Mycobacterium tuberculosis complex[1].
    Delamanid shows more potent antibacterial activity against drug-susceptible and drug-resistant strains of M. tuberculosis[2].
    Delamanid do not affect rifampin, pyrazinamide, and isoniazid exposure; the ethambutol AUCτ and Cmax values are about 25% higher with delamanid coadministration[3].

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

    In Vivo

    Delamanid (orally administration; 30 mg/kg; 5 days) results in sterile cures in a mouse model of VL[4].

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

    Clinical Trial
    Molecular Weight

    534.48

    Formula

    C25H25F3N4O6

    CAS No.
    Appearance

    Solid

    Color

    Off-white to yellow

    SMILES

    FC(F)(F)OC1=CC=C(OC2CCN(C3=CC=C(OC[C@@]4(C)CN5C(O4)=NC([N+]([O-])=O)=C5)C=C3)CC2)C=C1

    Shipping

    Room temperature in continental US; may vary elsewhere.

    Storage
    Powder -20°C 3 years
    4°C 2 years
    In solvent -80°C 2 years
    -20°C 1 year
    Solvent & Solubility
    In Vitro: 

    DMSO : 20 mg/mL (37.42 mM; ultrasonic and warming and heat to 60°C; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

    Ethanol : 2 mg/mL (3.74 mM; Need ultrasonic)

    Preparing
    Stock Solutions
    Concentration Solvent Mass 1 mg 5 mg 10 mg
    1 mM 1.8710 mL 9.3549 mL 18.7098 mL
    5 mM 0.3742 mL 1.8710 mL 3.7420 mL
    View the Complete Stock Solution Preparation Table

    * Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
    Storage method and period of stock solution: -80°C, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.

    • Molarity Calculator

    • Dilution Calculator

    Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

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    Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

    This equation is commonly abbreviated as: C1V1 = C2V2

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    In Vivo Dissolution Calculator
    Please enter the basic information of animal experiments:

    Dosage

    mg/kg

    Animal weight
    (per animal)

    g

    Dosing volume
    (per animal)

    μL

    Number of animals

    Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
    Calculation results:
    Working solution concentration: mg/mL
    Purity & Documentation

    Purity: 99.95%

    References

    Complete Stock Solution Preparation Table

    * Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
    Storage method and period of stock solution: -80°C, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.

    Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
    Ethanol / DMSO 1 mM 1.8710 mL 9.3549 mL 18.7098 mL 46.7744 mL
    DMSO 5 mM 0.3742 mL 1.8710 mL 3.7420 mL 9.3549 mL
    10 mM 0.1871 mL 0.9355 mL 1.8710 mL 4.6774 mL
    15 mM 0.1247 mL 0.6237 mL 1.2473 mL 3.1183 mL
    20 mM 0.0935 mL 0.4677 mL 0.9355 mL 2.3387 mL
    25 mM 0.0748 mL 0.3742 mL 0.7484 mL 1.8710 mL
    30 mM 0.0624 mL 0.3118 mL 0.6237 mL 1.5591 mL
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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:
    Delamanid
    Cat. No.:
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