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

Indimitecan  (Synonyms: LMP776)

製品番号: HY-18350 純度: 98.30%
COA 取扱説明書 Technical Support

Indimitecan (LMP776) is a topoisomerase I (Top1) inhibitor with anticancer activities.

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Indimitecan

Indimitecan 構造式

CAS 番号 : 915360-05-3

容量 価格(税別) 在庫状況 数量
5 mg $260 在庫あり
10 mg $400 在庫あり
25 mg $650 在庫あり
50 mg $910 在庫あり
100 mg $1280 在庫あり
200 mg   お問い合わせ  
500 mg   お問い合わせ  

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カスタマーレビュー

Based on 0 publication(s) in Google Scholar

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製品説明

Indimitecan (LMP776) is a topoisomerase I (Top1) inhibitor with anticancer activities[1].

IC50 & Target

Top1

 

Cellular Effect
Cell Line Type Value Description References
DU-145 GI50
<0.01 μM
Compound: 7, indimitecan
Antiproliferative activity against human DU145 cells by SRB assay
Antiproliferative activity against human DU145 cells by SRB assay
[PMID: 21710981]
DU-145 GI50
<0.01 μM
Compound: 6
Cytotoxicity against human DU145 cells
Cytotoxicity against human DU145 cells
[PMID: 20630766]
HCT-116 GI50
<0.01 μM
Compound: 7, indimitecan
Antiproliferative activity against human HCT116 cells by SRB assay
Antiproliferative activity against human HCT116 cells by SRB assay
[PMID: 21710981]
HCT-116 GI50
<0.01 μM
Compound: 6
Cytotoxicity against human HCT116 cells
Cytotoxicity against human HCT116 cells
[PMID: 20630766]
HOP-62 GI50
<0.01 μM
Compound: 7, indimitecan
Antiproliferative activity against human HOP62 cells by SRB assay
Antiproliferative activity against human HOP62 cells by SRB assay
[PMID: 21710981]
HOP-62 GI50
<0.01 μM
Compound: 6
Cytotoxicity against human HOP62 cells
Cytotoxicity against human HOP62 cells
[PMID: 20630766]
L1210 EC50
0.06 μM
Compound: 19
Trypanocidal activity against Trypanosoma brucei brucei 427 bloodstream forms infected in mouse L1210 cells after 48 hrs
Trypanocidal activity against Trypanosoma brucei brucei 427 bloodstream forms infected in mouse L1210 cells after 48 hrs
[PMID: 18824603]
MCF7 GI50
0.01 μM
Compound: 7, indimitecan
Antiproliferative activity against human MCF7 cells by SRB assay
Antiproliferative activity against human MCF7 cells by SRB assay
[PMID: 21710981]
MCF7 GI50
0.01 μM
Compound: 6
Cytotoxicity against human MCF7 cells
Cytotoxicity against human MCF7 cells
[PMID: 20630766]
OVCAR-3 GI50
0.085 μM
Compound: 7, indimitecan
Antiproliferative activity against human OVCAR3 cells by SRB assay
Antiproliferative activity against human OVCAR3 cells by SRB assay
[PMID: 21710981]
OVCAR-3 GI50
0.085 μM
Compound: 6
Cytotoxicity against human OVCAR-3 cells
Cytotoxicity against human OVCAR-3 cells
[PMID: 20630766]
SF-539 GI50
0.037 μM
Compound: 7, indimitecan
Antiproliferative activity against human SF539 cells by SRB assay
Antiproliferative activity against human SF539 cells by SRB assay
[PMID: 21710981]
SF-539 GI50
0.037 μM
Compound: 6
Cytotoxicity against human SF539 cells
Cytotoxicity against human SF539 cells
[PMID: 20630766]
SN12C GI50
<0.01 μM
Compound: 7, indimitecan
Antiproliferative activity against human SN12C cells by SRB assay
Antiproliferative activity against human SN12C cells by SRB assay
[PMID: 21710981]
SN12C GI50
<0.01 μM
Compound: 6
Cytotoxicity against human SN12C cells
Cytotoxicity against human SN12C cells
[PMID: 20630766]
UACC-62 GI50
<0.01 μM
Compound: 7, indimitecan
Antiproliferative activity against human UACC62 cells by SRB assay
Antiproliferative activity against human UACC62 cells by SRB assay
[PMID: 21710981]
UACC-62 GI50
<0.01 μM
Compound: 6
Cytotoxicity against human UACC62 cells
Cytotoxicity against human UACC62 cells
[PMID: 20630766]
体外実験

Indimitecan (LMP776) (0-100 μM) shows antiproliferative potencies against various human cancer cell lines, with mean-graph midpoint (MGM) of 0.079 ± 0.023 μM[1].
Indimitecan shows potent DNA cleavage due to Top1 inhibition[1].
Indimitecan can be substrates for metabolic ketone reductases[1].

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

Cell Proliferation Assay[1]

Cell Line: HOP-62, HCT-116, SF-539, UACC-62, OVCAR-3, SN12C, DU-145, MCF-7
Concentration: 0-100 μM
Incubation Time:
Result: Showed growth inhibition with GI50s of <0.01, <0.01, 0.04, <0.01, 0.08, <0.01, <0.01 and 0.01 μM against HOP-62, HCT-116, SF-539, UACC-62, OVCAR-3, SN12C, DU-145 and MCF-7 cells, respectively. And the mean-graph midpoint (MGM) for growth inhibition of all human cancer cell lines successfully tested (the National Cancer Institute’s developmental therapeutics assay (the “NCI60”)) was 0.079 ± 0.023 μM.
臨床実験
分子量

459.45

分子式

C25H21N3O6

CAS 番号
Appearance

Solid

Color

Brown to black

SMILES

O=C1C2=CC(OC)=C(OC)C=C2C3=C(C(C=C(OCO4)C4=C5)=C5C3=O)N1CCCN6C=NC=C6

輸送条件

Room temperature in continental US; may vary elsewhere.

保管条件
Powder -20°C 3 years
  4°C 2 years
In solvent -80°C 6 months
  -20°C 1 month
溶剤 & 溶解度
体外: 

DMSO : 8.33 mg/mL (18.13 mM; ultrasonic and warming and adjust pH to 3 with HCl and heat to 60°C; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 2.1765 mL 10.8826 mL 21.7652 mL
5 mM 0.4353 mL 2.1765 mL 4.3530 mL
10 mM 0.2177 mL 1.0883 mL 2.1765 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. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

  • Molarity Calculator

  • Dilution Calculator

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

Mass
=
Concentration
×
Volume
×
Molecular Weight *

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

一般には略語で表示されます:C1V1 = C2V2

濃度 (開始)

C1

×
体積 (開始)

V1

=
濃度 (終了)

C2

×
体積 (終了)

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
純度とドキュメンテーション

純度: 98.30%

参考文献

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. 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 1 mM 2.1765 mL 10.8826 mL 21.7652 mL 54.4129 mL
5 mM 0.4353 mL 2.1765 mL 4.3530 mL 10.8826 mL
10 mM 0.2177 mL 1.0883 mL 2.1765 mL 5.4413 mL
15 mM 0.1451 mL 0.7255 mL 1.4510 mL 3.6275 mL
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  • Molarity Calculator

  • Dilution Calculator

The molarity calculator equation

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

質量   濃度   体積   分子量 *
= × ×

The dilution calculator equation

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

一般には略語で表示されます:C1V1 = C2V2

濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)
× = ×
C1   V1   C2   V2
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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Inquiry Information

製品名:
Indimitecan
製品番号:
HY-18350
数量:
MCE 日本正規代理店: