1. Cell Cycle/DNA Damage
  2. Topoisomerase
  3. Bisantrene

Bisantrene is a highly effective antitumor agent, it exerts its cytotoxicity by affecting DNA intercalation. Bisantrene targets eukaryotic type II topoisomerases. Bisantrene is a substrate of MDR1.

연구목적의 판매만을 진행합니다. 환자를 대상으로 한 판매는 하지 않습니다.

Bisantrene

Bisantrene 화학구조

CAS No. : 78186-34-2

사이즈 가격 재고 수량
5 mg 해외재고보유
10 mg 해외재고보유
25 mg 해외재고보유
50 mg 해외재고보유
100 mg   견적 받기  
200 mg   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 6 publication(s) in Google Scholar

Other Forms of Bisantrene:

Top Publications Citing Use of Products

View All Topoisomerase Isoform Specific Products:

  • Biological Activity

  • Protocol

  • 순도&문서

  • References

  • 고객리뷰

제품 설명

Bisantrene is a highly effective antitumor agent, it exerts its cytotoxicity by affecting DNA intercalation. Bisantrene targets eukaryotic type II topoisomerases. Bisantrene is a substrate of MDR1[1][2][3][4].

IC50 & Target[1]

Topoisomerase II

 

Cellular Effect
Cell Line Type Value Description References
A2780 IC50
0.34 3
Compound: Bisantrene
Cell cytotoxicity was determined against human ovarian cancer (A2780) cell line
Cell cytotoxicity was determined against human ovarian cancer (A2780) cell line
[PMID: 9871638]
A2780 IC50
0.34 3
Compound: Bisantrene
Cell cytotoxicity was determined against human ovarian cancer (A2780) cell line
Cell cytotoxicity was determined against human ovarian cancer (A2780) cell line
[PMID: 9871638]
A549 IC50
0.017 3
Compound: 1
Compound was tested for potency against human lung A549 cells using sulforhodamine B assay.
Compound was tested for potency against human lung A549 cells using sulforhodamine B assay.
[PMID: 9371238]
RPMI-8226 IC50
0.018 3
Compound: 1
Compound was tested for potency against human myeloma 8226 cells using MTT assay method.
Compound was tested for potency against human myeloma 8226 cells using MTT assay method.
[PMID: 9371238]
A549 IC50
0.017 3
Compound: 1
Compound was tested for potency against human lung A549 cells using sulforhodamine B assay.
Compound was tested for potency against human lung A549 cells using sulforhodamine B assay.
[PMID: 9371238]
A549 IC50
0.017 3
Compound: 1
Compound was tested for potency against human lung A549 cells using sulforhodamine B assay.
Compound was tested for potency against human lung A549 cells using sulforhodamine B assay.
[PMID: 9371238]
HL-60 IC50
0.3 3
Compound: Bisantrene
Cell cytotoxicity was determined against human promyelocytic leukemia (HL60) cell line
Cell cytotoxicity was determined against human promyelocytic leukemia (HL60) cell line
[PMID: 9871638]
HL-60 IC50
0.3 3
Compound: Bisantrene
Cell cytotoxicity was determined against human promyelocytic leukemia (HL60) cell line
Cell cytotoxicity was determined against human promyelocytic leukemia (HL60) cell line
[PMID: 9871638]
L1210 IC50
3.2 3
Compound: 1
Compound was tested for potency against multi drug resistant murine leukemia L1210 cells.
Compound was tested for potency against multi drug resistant murine leukemia L1210 cells.
[PMID: 9371238]
L1210 IC50
0.049 3
Compound: 1
Compound was tested for potency against multidrug-resistant murine leukemia L1210 cells
Compound was tested for potency against multidrug-resistant murine leukemia L1210 cells
[PMID: 9371238]
L1210 IC50
0.049 3
Compound: 1
Compound was tested for potency against multidrug-resistant murine leukemia L1210 cells
Compound was tested for potency against multidrug-resistant murine leukemia L1210 cells
[PMID: 9371238]
L1210 IC50
3.2 3
Compound: 1
Compound was tested for potency against multi drug resistant murine leukemia L1210 cells.
Compound was tested for potency against multi drug resistant murine leukemia L1210 cells.
[PMID: 9371238]
RPMI-8226 IC50
9.1 3
Compound: 1
Compound was tested for potency against human myeloma 8226 cells (40 fold resistant to doxorubicin).
Compound was tested for potency against human myeloma 8226 cells (40 fold resistant to doxorubicin).
[PMID: 9371238]
RPMI-8226 IC50
0.018 3
Compound: 1
Compound was tested for potency against human myeloma 8226 cells using MTT assay method.
Compound was tested for potency against human myeloma 8226 cells using MTT assay method.
[PMID: 9371238]
SW480 IC50
0.09 3
Compound: 1
Compound was tested for potency against human colon carcinoma SW 480 cells in a sulforhodamine B assay.
Compound was tested for potency against human colon carcinoma SW 480 cells in a sulforhodamine B assay.
[PMID: 9371238]
WiDr IC50
0.79 3
Compound: 1
Compound was tested for potency against human colon carcinoma WiDr cells in a sulforhodamine B assay.
Compound was tested for potency against human colon carcinoma WiDr cells in a sulforhodamine B assay.
[PMID: 9371238]
OCI-AML2 IC50
100 1
Compound: 39; CS1
Antiproliferative activity against human OCI-AML2 cells assessed as reduction in cell viability
Antiproliferative activity against human OCI-AML2 cells assessed as reduction in cell viability
[PMID: 38805939]
RPMI-8226 IC50
0.018 3
Compound: 1
Compound was tested for potency against human myeloma 8226 cells using MTT assay method.
Compound was tested for potency against human myeloma 8226 cells using MTT assay method.
[PMID: 9371238]
RPMI-8226 IC50
9.1 3
Compound: 1
Compound was tested for potency against human myeloma 8226 cells (40 fold resistant to doxorubicin).
Compound was tested for potency against human myeloma 8226 cells (40 fold resistant to doxorubicin).
[PMID: 9371238]
SW480 IC50
0.09 3
Compound: 1
Compound was tested for potency against human colon carcinoma SW 480 cells in a sulforhodamine B assay.
Compound was tested for potency against human colon carcinoma SW 480 cells in a sulforhodamine B assay.
[PMID: 9371238]
WiDr IC50
0.79 3
Compound: 1
Compound was tested for potency against human colon carcinoma WiDr cells in a sulforhodamine B assay.
Compound was tested for potency against human colon carcinoma WiDr cells in a sulforhodamine B assay.
[PMID: 9371238]
In Vitro

Bisantrene promots DNase I cleavage at oligopurine-oligopyrimidine tracts and slightly reduces the cleavage activity at alternating purine-pyrimidine sequences[1].
? Bisantrene is an inhibitor of [3H]uridine incorporation into RNA and [3H]thymidine incorporation into DNA[2].

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

In Vivo

Bisantrene is an antitumor agent active against a number of experimental tumors, including P388 leukemia, L1210 leukemia, Lieberman plasma cell tumor, B16 melanoma, colon tumor 26, and Ridgway osteogenic sarcoma[3].
? Bisantrene is effective over a dose range of 1.56 to 150 mg/kg depending upon the frequency, route, and schedule of the treatment and the tumor model used[3].
? Bisantrene (25, 50 and 100 mg/kg; i.p.; once) pretreats with macrophages shows antitumor effect to mice with P815 tumor cells injection[3].
? Bisantrene (10-150 mg/kg; i.v.; once) dose-dependently induces leukopenia in Neo mice. B cells and macrophages are targets for bisantrene toxicity[4].

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

Clinical Trial
분자량

398.46

화학식

C22H22N8

CAS No.
Appearance

Solid

Color

Orange to red

SMILES

C12=CC=CC=C1C(/C=N/NC3=NCCN3)=C4C(C=CC=C4)=C2/C=N/NC5=NCCN5

선적

Room temperature in continental US; may vary elsewhere.

보관
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 2 years
-20°C 1 year
용액&용해도
In Vitro: 

DMSO : 1 mg/mL (2.51 mM; ultrasonic and warming and heat to 80°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 2.5097 mL 12.5483 mL 25.0966 mL
5 mM --- --- ---
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.

  • 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 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: 98.06%

References
Kinase Assay
[1]

Measurements are carried out at 25°C in ETN buffer (1 mM EDTA, 10 mM Tris, pH 7.0, with NaCl to obtain the desired ionic strength). Binding is monitored spectrophotometrically or fluorometrically, in the ligand absorption or emission region, respectively, after addition of scalar amounts of DNA to a freshly prepared drug solution. To avoid large systematic inaccuracies resulting from experimental errors in extinction coefficients or fluorescence quantum yield, the range of bound drug fractions is 0.15-0.85. Data are evaluated. Spectroscopic measurements are made with a Perkin-Elmer Lambda 5 apparatus and a MPF66 fluorometer, both equipped with a Haake F3-C thermostat[1].

MCE 는 독립적으로 이러한 방법들의 정확성을 확인하지 않았습니다. 참고용으로만 봐주십시오.

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
DMSO 1 mM 2.5097 mL 12.5483 mL 25.0966 mL 62.7416 mL
  • No file chosen (Maximum size is: 1024 Kb)
  • If you have published this work, please enter the PubMed ID.
  • Your name will appear on the site.
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.

최근 본 상품:

온라인 문의

Your information is safe with us. * Required Fields.

상품명

 

Requested Quantity *

고객명 *

 

호칭

메일주소 *

 

전화번호 *

Department

 

회사명 *

City

Country or Region *

     

비고

대량구매 문의

Inquiry Information

상품명:
Bisantrene
Cat. No.:
HY-100875
수량:
MCE Japan Authorized Agent: