1. Cell Cycle/DNA Damage Apoptosis MAPK/ERK Pathway GPCR/G Protein
  2. G-quadruplex Bcl-2 Family Ras Caspase
  3. MM41

MM41 is a quadruplex-interacting compound. MM41 binds tightly to quadruplexes encoded in the promoter sequences of the BCL-2 and k-RAS genes. MM41 reduces BCL-2 and k-RAS protein levels, increases caspase 3. MM41 has antitumor effects against pancreatic cancer.

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MM41

MM41 화학구조

CAS No. : 1429028-96-5

사이즈 가격 재고 수량
무료 샘플 (0.1 - 0.2 mg)   지금 신청하기  
5 mg 해외재고보유
10 mg 해외재고보유
25 mg 해외재고보유
50 mg 해외재고보유
100 mg 해외재고보유
200 mg   견적 받기  
500 mg   견적 받기  

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

고객리뷰

Based on 1 publication(s) in Google Scholar

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  • Biological Activity

  • 순도&문서

  • References

  • 고객리뷰

제품 설명

MM41 is a quadruplex-interacting compound. MM41 binds tightly to quadruplexes encoded in the promoter sequences of the BCL-2 and k-RAS genes. MM41 reduces BCL-2 and k-RAS protein levels, increases caspase 3. MM41 has antitumor effects against pancreatic cancer[1].

IC50 & Target[1]

Caspase 3

 

Bcl-2

 

K-RAS

 

Cellular Effect
Cell Line Type Value Description References
786-0 IC50
0.32 μM
Compound: 3d
Cytotoxicity against human 786-0 cells assessed as growth inhibition after 96 hrs by SRB assay
Cytotoxicity against human 786-0 cells assessed as growth inhibition after 96 hrs by SRB assay
[PMID: 23514618]
A549 IC50
19 nM
Compound: MM41
Growth inhibition of human A549 cells after 96 hrs by SRB assay
Growth inhibition of human A549 cells after 96 hrs by SRB assay
[PMID: 29356532]
A549 IC50
< 0.01 μM
Compound: 3d
Cytotoxicity against human A549 cells assessed as growth inhibition after 96 hrs by SRB assay
Cytotoxicity against human A549 cells assessed as growth inhibition after 96 hrs by SRB assay
[PMID: 23514618]
MCF7 IC50
0.07 μM
Compound: 3d
Cytotoxicity against human MCF7 cells assessed as growth inhibition after 96 hrs by SRB assay
Cytotoxicity against human MCF7 cells assessed as growth inhibition after 96 hrs by SRB assay
[PMID: 23514618]
MCF7 IC50
70 nM
Compound: MM41
Growth inhibition of human MCF7 cells after 96 hrs by SRB assay
Growth inhibition of human MCF7 cells after 96 hrs by SRB assay
[PMID: 29356532]
MIA PaCa-2 IC50
0.01 μM
Compound: 3d
Cytotoxicity against human MIAPaCa2 cells assessed as growth inhibition after 96 hrs by SRB assay
Cytotoxicity against human MIAPaCa2 cells assessed as growth inhibition after 96 hrs by SRB assay
[PMID: 23514618]
MIA PaCa-2 IC50
11 nM
Compound: MM41
Growth inhibition of human MIAPaCa2 cells after 96 hrs by SRB assay
Growth inhibition of human MIAPaCa2 cells after 96 hrs by SRB assay
[PMID: 29356532]
PANC-1 IC50
0.003 μM
Compound: 2a
Cytotoxicity against human PANC1 cells after 96 hrs by SRB assay
Cytotoxicity against human PANC1 cells after 96 hrs by SRB assay
[PMID: 23769166]
PANC-1 IC50
3 nM
Compound: MM41
Growth inhibition of human PANC1 cells after 96 hrs by SRB assay
Growth inhibition of human PANC1 cells after 96 hrs by SRB assay
[PMID: 29356532]
RCC4 IC50
0.56 μM
Compound: 3d
Cytotoxicity against human RCC4 cells assessed as growth inhibition after 96 hrs by SRB assay
Cytotoxicity against human RCC4 cells assessed as growth inhibition after 96 hrs by SRB assay
[PMID: 23514618]
WI-38 IC50
0.23 μM
Compound: 3d
Cytotoxicity against human WI38 cells assessed as growth inhibition after 96 hrs by SRB assay
Cytotoxicity against human WI38 cells assessed as growth inhibition after 96 hrs by SRB assay
[PMID: 23514618]
WI-38 IC50
230 nM
Compound: MM41
Growth inhibition of human WI38 cells after 96 hrs by SRB assay
Growth inhibition of human WI38 cells after 96 hrs by SRB assay
[PMID: 29356532]
In Vitro

MM41 (1 μM) stabilizes the BCL-2 promoter G-quadruplex with a ΔTₘ value of 26.4 °C, and also binds effectively to k-RAS1 and k-RAS2 promoter G-quadruplexes with ΔTₘ values of 22.5 °C and 19.8 °C respectively[1].

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

In Vivo

MM41 (10-15 mg/kg; i.v.; twice weekly; 12 doses) shows dose-dependent anti-tumour activity in MIA PaCa-2 pancreatic cancer xenografts[1].

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

Animal Model: Female CD-1 nude mice (2-3 months old, weighing 20-25 g) bearing MIA PaCa-2 pancreatic cancer subcutaneous xenografts[1]
Dosage: 10 mg/kg, 15 mg/kg
Administration: Intravenous administration, twice weekly, 12 doses
Result: Resulted in an average reduction of ca 80% in tumor growth by day 40 in mice, cessation of tumor regrowth from day 30 onwards, and complete tumor regression in two mice with no regrowth for 239 days (15 mg/kg).
Showed weaker anti-tumour effect (10 mg/kg).
Showed reduced BCL-2 and k-RAS protein levels in treated tumours.
Showed that treated tumours, but not untreated ones, show high levels of caspase 3 staining.
분자량

831.06

화학식

C44H66N10O6

CAS No.
Appearance

Solid

Color

Blue to purple

SMILES

O=C1C2=CC(NCCCN3CCN(CC3)C)=C4C(N(CCCN5CCOCC5)C(C6=CC(NCCCN7CCN(CC7)C)=C(C2=C64)C(N1CCCN8CCOCC8)=O)=O)=O

선적

Room temperature in continental US; may vary elsewhere.

보관
Powder -20°C 3 years
In solvent -80°C 6 months
-20°C 1 month
용액&용해도
In Vitro: 

1 M HCl : 100 mg/mL (120.33 mM; Need ultrasonic)

DMSO : 33.33 mg/mL (40.11 mM; ultrasonic and adjust pH to 8 with HCl; 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 1.2033 mL 6.0164 mL 12.0328 mL
5 mM 0.2407 mL 1.2033 mL 2.4066 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.

  • 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
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. 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 M HCl 1 mM 1.2033 mL 6.0164 mL 12.0328 mL 30.0821 mL
5 mM 0.2407 mL 1.2033 mL 2.4066 mL 6.0164 mL
10 mM 0.1203 mL 0.6016 mL 1.2033 mL 3.0082 mL
15 mM 0.0802 mL 0.4011 mL 0.8022 mL 2.0055 mL
20 mM 0.0602 mL 0.3008 mL 0.6016 mL 1.5041 mL
25 mM 0.0481 mL 0.2407 mL 0.4813 mL 1.2033 mL
30 mM 0.0401 mL 0.2005 mL 0.4011 mL 1.0027 mL
40 mM 0.0301 mL 0.1504 mL 0.3008 mL 0.7521 mL
1 M HCl 50 mM 0.0241 mL 0.1203 mL 0.2407 mL 0.6016 mL
60 mM 0.0201 mL 0.1003 mL 0.2005 mL 0.5014 mL
80 mM 0.0150 mL 0.0752 mL 0.1504 mL 0.3760 mL
100 mM 0.0120 mL 0.0602 mL 0.1203 mL 0.3008 mL
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상품명:
MM41
Cat. No.:
HY-16967
수량:
MCE Japan Authorized Agent: