1. Cell Cycle/DNA Damage Apoptosis
  2. Nucleoside Antimetabolite/Analog Apoptosis
  3. Dacarbazine

Dacarbazine  (Synonyms: Imidazole Carboxamide)

Cat. No.: HY-B0078 Purity: 99.96%
Handling Instructions Technical Support

Dacarbazine is a nonspecific antineoplastic (antineoplastic) alkylating agent. Dacarbazine inhibits T and B lymphocyte responses with IC50 of 50 and 10 μg/mL, respectively. Dacarbazine can be used in the study of metastatic malignant melanoma.

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CAS No. : 4342-03-4

사이즈 가격 재고 수량
Solid + Solvent (Highly Recommended)
10 mM * 1 mL in DMSO
ready for reconstitution
해외재고보유
Solution
10 mM * 1 mL in DMSO 해외재고보유
Solid
50 mg 해외재고보유
100 mg 해외재고보유
200 mg 해외재고보유
1 g 해외재고보유
5 g   견적 받기  
10 g   견적 받기  

* 장바구니에 담기 전 물품의 수량을 선택해 주십시오.

This product is a controlled substance and not for sale in your territory.

고객리뷰

Based on 15 publication(s) in Google Scholar

Other Forms of Dacarbazine:

Top Publications Citing Use of Products

    Dacarbazine purchased from MedChemExpress. Usage Cited in: Cell Death Dis. 2025 Apr 9;16(1):268.  [Abstract]

    Dacarbazine (20 mg/kg; i.p.; 20 d) reduced tumor growth rates and tumor sizes of melanoma xenograft mice.

    Dacarbazine purchased from MedChemExpress. Usage Cited in: Adv Sci (Weinh). 2024 Dec;11(48):e2408707.  [Abstract]

    Dacarbazine (DTIC) (500 µM; 72 h) reduced the diameter and metabolic activity of MCTs except monoculture tumoroids, especially the triples and quadruples, resulting in a decrease of approximately 32% and 28% in relative diameter, respectively, and caused a high number of apoptotic cells to detach from the main structure.

    Dacarbazine purchased from MedChemExpress. Usage Cited in: Nature. 2023 Jun;618(7964):374-382.  [Abstract]

    Dacarbazine (60 mg/kg; i.p.; every other day for 8 d) significantly reduced red blood cell (RBC), reticulocyte (RET), and hemoglobin (HGB) counts in PBS- or B16F10-CL-EVP-educated mice.

    Dacarbazine purchased from MedChemExpress. Usage Cited in: J Nanobiotechnology. 2023 Oct 19;21(1):383.  [Abstract]

    Dacarbazine (DAC) (5 mg/kg; i.v.; once every three days for 3 times) significantly inhibited the growth of subcutaneous B16F10 melanoma xenografts in C57BL/6 mice.

    Dacarbazine purchased from MedChemExpress. Usage Cited in: J Nanobiotechnology. 2023 Oct 19;21(1):383.  [Abstract]

    H&E staining of tumors in each group at the end of treatment. The results showed that Dacarbazine (DAC) (5 mg/kg; i.v.; once every three days for 3 times) caused significant cell necrosis and nucleopaenia in tumors of B16F10 tumor-bearing mice. Scale bar, 100 μm.
    • Biological Activity

    • 순도&문서

    • References

    • 고객리뷰

    제품 설명

    Dacarbazine is a nonspecific antineoplastic (antineoplastic) alkylating agent. Dacarbazine inhibits T and B lymphocyte responses with IC50 of 50 and 10 μg/mL, respectively. Dacarbazine can be used in the study of metastatic malignant melanoma[1][2][3][4][5].

    Cellular Effect
    Cell Line Type Value Description References
    A-375 IC50
    > 100 μM
    Compound: DTIC
    Antiproliferative activity against human A375 cells after 48 hrs by SRB assay
    Antiproliferative activity against human A375 cells after 48 hrs by SRB assay
    [PMID: 20056548]
    A-375 IC50
    > 100 μM
    Compound: DTIC, dacarbazine
    Antiproliferative activity against human A375 cells after 48 hrs by SRB assay
    Antiproliferative activity against human A375 cells after 48 hrs by SRB assay
    [PMID: 18477505]
    A-375 IC50
    > 500 μM
    Compound: dacarbazine
    Cytotoxicity against human A375 cells after 48 hrs by MTT assay
    Cytotoxicity against human A375 cells after 48 hrs by MTT assay
    [PMID: 22560315]
    A549 IC50
    35 μg/mL
    Compound: Dacarbazine
    Cytotoxicity against Homo sapiens (human) A549 cells assessed as cell viability by MTT assay
    Cytotoxicity against Homo sapiens (human) A549 cells assessed as cell viability by MTT assay
    10.1007/s00044-007-9031-x
    B16-F1 IC50
    > 100 μM
    Compound: DTIC
    Antiproliferative activity against mouse B16-F1 cells after 48 hrs by SRB assay
    Antiproliferative activity against mouse B16-F1 cells after 48 hrs by SRB assay
    [PMID: 20056548]
    B16-F1 IC50
    > 100 μM
    Compound: DTIC, dacarbazine
    Antiproliferative activity against mouse B16-F1 cells after 48 hrs by SRB assay
    Antiproliferative activity against mouse B16-F1 cells after 48 hrs by SRB assay
    [PMID: 18477505]
    Fibroblast IC50
    > 100 μM
    Compound: DTIC
    Cytotoxicity against human fibroblasts after 48 hrs by SRB assay
    Cytotoxicity against human fibroblasts after 48 hrs by SRB assay
    [PMID: 20056548]
    HeLa GI50
    > 50 μM
    Compound: DTIC
    Cytotoxicity against human HeLa cells assessed as reduction in cell viability after 24 to 48 hrs by MTT assay
    Cytotoxicity against human HeLa cells assessed as reduction in cell viability after 24 to 48 hrs by MTT assay
    [PMID: 24986661]
    MDA-MB-435 GI50
    84.33 μM
    Compound: Dacarbazine
    Growth inhibition of human MDA-MB-435 cells measured after 24 to 72 hrs by SRB method
    Growth inhibition of human MDA-MB-435 cells measured after 24 to 72 hrs by SRB method
    [PMID: 37163949]
    OVCAR-3 IC50
    17.67 μM
    Compound: Dacarbazine
    Cytotoxicity against human OVCAR3 cells after 6 days by MTT assay
    Cytotoxicity against human OVCAR3 cells after 6 days by MTT assay
    [PMID: 21131205]
    Raji IC50
    128 μM
    Compound: DTIC
    In vitro cytotoxicity against Raji cell line
    In vitro cytotoxicity against Raji cell line
    [PMID: 7739008]
    SK-MEL-2 IC50
    120 μM
    Compound: Dacarbazine
    Cytotoxicity against human SK-MEL-2 cells after 6 days by MTT assay
    Cytotoxicity against human SK-MEL-2 cells after 6 days by MTT assay
    [PMID: 21131205]
    SK-MEL-28 GI50
    > 100 μM
    Compound: Dacarbazine
    Growth inhibition of human SK-MEL-28 cells measured after 24 to 72 hrs by SRB method
    Growth inhibition of human SK-MEL-28 cells measured after 24 to 72 hrs by SRB method
    [PMID: 37163949]
    UACC-62 IC50
    11.83 μM
    Compound: Dacarbazine
    Cytotoxicity against human UACC62 cells after 6 days by MTT assay
    Cytotoxicity against human UACC62 cells after 6 days by MTT assay
    [PMID: 21131205]
    WM164 IC50
    > 100 μM
    Compound: DTIC
    Antiproliferative activity against human WM164 cells after 48 hrs by SRB assay
    Antiproliferative activity against human WM164 cells after 48 hrs by SRB assay
    [PMID: 17561392]
    WM164 IC50
    > 100 μM
    Compound: DTIC
    Antiproliferative activity against human WM164 cells after 48 hrs by SRB assay
    Antiproliferative activity against human WM164 cells after 48 hrs by SRB assay
    [PMID: 20056548]
    In Vitro

    Dacarbazine (6.25-500 μg/mL 48 h) combines with hyperthermia-induced cytotoxicity of A375 and MNT-1 melanoma cells[5].

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

    Cell Viability Assay[5]

    Cell Line: A375, MNT-1
    Concentration: 6.25, 12.5, 25, 50, 100, 200, 400, 500 μg/mL
    Incubation Time: 24, 48, 72 h
    Result: Inhibited cell viability in a concentration-dependent manner.

    Cell Cycle Analysis[5]

    Cell Line: A375, MNT-1
    Concentration: 5.5, 115 μg/mL
    Incubation Time: 48 h
    Result: Decreased (9.3%) the percentage of A375 cells at the S phase and increased the number of cells at G2/M.
    Decreased MNT-1 cells at G0/G1, increasing in cells at both S and G2/M phases.
    Clinical Trial
    분자량

    182.18

    화학식

    C6H10N6O

    CAS No.
    Appearance

    Solid

    Color

    White to yellow

    SMILES

    O=C(C1=C(/N=N/N(C)C)NC=N1)N

    선적

    Room temperature in continental US; may vary elsewhere.

    보관

    4°C, protect from light

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

    용액&용해도
    In Vitro: 

    0.1 M HCl : 20 mg/mL (109.78 mM; ultrasonic and warming and heat to 60°C)

    DMSO : 5 mg/mL (27.45 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)

    H2O : < 0.1 mg/mL (insoluble)

    Preparing
    Stock Solutions
    Concentration Solvent Mass 1 mg 5 mg 10 mg
    1 mM 5.4891 mL 27.4454 mL 54.8908 mL
    5 mM 1.0978 mL 5.4891 mL 10.9782 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, 6 months; -20°C, 1 month (protect from light). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

    • 몰농도 계산기

    • 농도 희석 계산기

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

    Mass
    =
    Concentration
    ×
    Volume
    ×
    Molecular Weight *

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

    This equation is commonly abbreviated as: C1V1 = C2V2

    Concentration (start)

    C1

    ×
    Volume (start)

    V1

    =
    Concentration (final)

    C2

    ×
    Volume (final)

    V2

    In Vivo:

    For the following dissolution methods, please prepare the working solution directly. It is recommended to prepare fresh solutions and use them promptly within a short period of time.
    The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.

    • Protocol 1

      Add each solvent one by one:  PBS

      Solubility: 2 mg/mL (10.98 mM); Clear solution; Need ultrasonic and warming and heat to 60°C

    • Protocol 2

      Add each solvent one by one:  50% PEG300    50% Saline

      Solubility: 5 mg/mL (27.45 mM); Suspended solution; Need ultrasonic

    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
    순도&문서

    Purity: 99.96%

    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, 6 months; -20°C, 1 month (protect from light). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

    Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
    DMSO / 0.1 M HCl 1 mM 5.4891 mL 27.4454 mL 54.8908 mL 137.2269 mL
    5 mM 1.0978 mL 5.4891 mL 10.9782 mL 27.4454 mL
    10 mM 0.5489 mL 2.7445 mL 5.4891 mL 13.7227 mL
    15 mM 0.3659 mL 1.8297 mL 3.6594 mL 9.1485 mL
    20 mM 0.2745 mL 1.3723 mL 2.7445 mL 6.8613 mL
    25 mM 0.2196 mL 1.0978 mL 2.1956 mL 5.4891 mL
    0.1 M HCl 30 mM 0.1830 mL 0.9148 mL 1.8297 mL 4.5742 mL
    40 mM 0.1372 mL 0.6861 mL 1.3723 mL 3.4307 mL
    50 mM 0.1098 mL 0.5489 mL 1.0978 mL 2.7445 mL
    60 mM 0.0915 mL 0.4574 mL 0.9148 mL 2.2871 mL
    80 mM 0.0686 mL 0.3431 mL 0.6861 mL 1.7153 mL
    100 mM 0.0549 mL 0.2745 mL 0.5489 mL 1.3723 mL
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    • 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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    상품명:
    Dacarbazine
    Cat. No.:
    HY-B0078
    수량:
    MCE Japan Authorized Agent: