BLK-IN-2
Based on 1 Customer Validation
BLK-IN-2 (compound 25) is a potent and selective irreversible inhibitor of B-Lymphoid tyrosine kinase (BLK), with an IC50 of 5.9 nM. BLK-IN-2 also inhibits BTK (IC50=202.0 nM). BLK-IN-2 shows potent antiproliferative activities against several lymphoma cells.
연구목적의 판매만을 진행합니다. 환자를 대상으로 한 판매는 하지 않습니다.
- Purity: 98.61%
- CAS No.: 2694871-86-6
- 화학식: C39H41N9O3
- 분자량:683.80
-
보관:Powder -20°C, 3 years , 4°C, 2 years ; In solvent -80°C, 6 months , -20°C, 1 month
Biological Activity
|
Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| A-375 | GI50 |
>30 μM
Compound: 25
|
Antiproliferative activity against human A-375 cells assessed as cell growth inhibition incubated for 72 hrs by celltiter-glo luminescent cell viability assay
Antiproliferative activity against human A-375 cells assessed as cell growth inhibition incubated for 72 hrs by celltiter-glo luminescent cell viability assay
|
[PMID: 34952433] |
| A-431 | GI50 |
>30 μM
Compound: 25
|
Antiproliferative activity against human A-431 cells assessed as cell growth inhibition incubated for 72 hrs by celltiter-glo luminescent cell viability assay
Antiproliferative activity against human A-431 cells assessed as cell growth inhibition incubated for 72 hrs by celltiter-glo luminescent cell viability assay
|
[PMID: 34952433] |
| A549 | GI50 |
>30 μM
Compound: 25
|
Antiproliferative activity against human A549 cells assessed as cell growth inhibition incubated for 72 hrs by celltiter-glo luminescent cell viability assay
Antiproliferative activity against human A549 cells assessed as cell growth inhibition incubated for 72 hrs by celltiter-glo luminescent cell viability assay
|
[PMID: 34952433] |
| DOHH-2 | GI50 |
0.016 μM
Compound: 25
|
Antiproliferative activity against human DOHH-2 cells assessed as cell growth inhibition incubated for 72 hrs by celltiter-glo luminescent cell viability assay
Antiproliferative activity against human DOHH-2 cells assessed as cell growth inhibition incubated for 72 hrs by celltiter-glo luminescent cell viability assay
|
[PMID: 34952433] |
| HBL1 | GI50 |
1.34 μM
Compound: 25
|
Antiproliferative activity against human HBL1 cells assessed as cell growth inhibition incubated for 72 hrs by celltiter-glo luminescent cell viability assay
Antiproliferative activity against human HBL1 cells assessed as cell growth inhibition incubated for 72 hrs by celltiter-glo luminescent cell viability assay
|
[PMID: 34952433] |
| HCT-116 | GI50 |
8.1 μM
Compound: 25
|
Antiproliferative activity against human HCT-116 cells assessed as cell growth inhibition incubated for 72 hrs by celltiter-glo luminescent cell viability assay
Antiproliferative activity against human HCT-116 cells assessed as cell growth inhibition incubated for 72 hrs by celltiter-glo luminescent cell viability assay
|
[PMID: 34952433] |
| HEK293 | GI50 |
>30 μM
Compound: 25
|
Antiproliferative activity against HEK293 cells assessed as cell growth inhibition incubated for 72 hrs by celltiter-glo luminescent cell viability assay
Antiproliferative activity against HEK293 cells assessed as cell growth inhibition incubated for 72 hrs by celltiter-glo luminescent cell viability assay
|
[PMID: 34952433] |
| Jurkat | GI50 |
10.9 μM
Compound: 25
|
Antiproliferative activity against human Jurkat cells assessed as cell growth inhibition incubated for 72 hrs by celltiter-glo luminescent cell viability assay
Antiproliferative activity against human Jurkat cells assessed as cell growth inhibition incubated for 72 hrs by celltiter-glo luminescent cell viability assay
|
[PMID: 34952433] |
| MDA-MB-453 | GI50 |
>30 μM
Compound: 25
|
Antiproliferative activity against human MDA-MB-453 cells assessed as cell growth inhibition incubated for 72 hrs by celltiter-glo luminescent cell viability assay
Antiproliferative activity against human MDA-MB-453 cells assessed as cell growth inhibition incubated for 72 hrs by celltiter-glo luminescent cell viability assay
|
[PMID: 34952433] |
| MOLT-4 | GI50 |
18.8 μM
Compound: 25
|
Antiproliferative activity against human MOLT-4 cells assessed as cell growth inhibition incubated for 72 hrs by celltiter-glo luminescent cell viability assay
Antiproliferative activity against human MOLT-4 cells assessed as cell growth inhibition incubated for 72 hrs by celltiter-glo luminescent cell viability assay
|
[PMID: 34952433] |
| OCI-Ly7 | GI50 |
0.02 μM
Compound: 25
|
Antiproliferative activity against human OCILY7 cells assessed as cell growth inhibition incubated for 72 hrs by celltiter-glo luminescent cell viability assay
Antiproliferative activity against human OCILY7 cells assessed as cell growth inhibition incubated for 72 hrs by celltiter-glo luminescent cell viability assay
|
[PMID: 34952433] |
| PBMC | GI50 |
>30 μM
Compound: 25
|
Antiproliferative activity against human PBMC cells assessed as cell growth inhibition incubated for 72 hrs by celltiter-glo luminescent cell viability assay
Antiproliferative activity against human PBMC cells assessed as cell growth inhibition incubated for 72 hrs by celltiter-glo luminescent cell viability assay
|
[PMID: 34952433] |
| Pfeiffer | GI50 |
2.18 μM
Compound: 25
|
Antiproliferative activity against human Pfeiffer cells assessed as cell growth inhibition incubated for 72 hrs by celltiter-glo luminescent cell viability assay
Antiproliferative activity against human Pfeiffer cells assessed as cell growth inhibition incubated for 72 hrs by celltiter-glo luminescent cell viability assay
|
[PMID: 34952433] |
| SU-DHL10 | GI50 |
0.56 μM
Compound: 25
|
Antiproliferative activity against human SU-DHL-10 cells assessed as cell growth inhibition incubated for 72 hrs by celltiter-glo luminescent cell viability assay
Antiproliferative activity against human SU-DHL-10 cells assessed as cell growth inhibition incubated for 72 hrs by celltiter-glo luminescent cell viability assay
|
[PMID: 34952433] |
| SU-DHL-6 | GI50 |
0.13 μM
Compound: 25
|
Antiproliferative activity against human SU-DHL-6 cells assessed as cell growth inhibition incubated for 72 hrs by celltiter-glo luminescent cell viability assay
Antiproliferative activity against human SU-DHL-6 cells assessed as cell growth inhibition incubated for 72 hrs by celltiter-glo luminescent cell viability assay
|
[PMID: 34952433] |
| TMD8 | GI50 |
0.064 μM
Compound: 25
|
Antiproliferative activity against human TMD8 cells assessed as cell growth inhibition incubated for 72 hrs by celltiter-glo luminescent cell viability assay
Antiproliferative activity against human TMD8 cells assessed as cell growth inhibition incubated for 72 hrs by celltiter-glo luminescent cell viability assay
|
[PMID: 34952433] |
Chemical Information
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CAS No. 2694871-86-6
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Appearance Solid
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분자량 683.80
-
화학식 C39H41N9O3
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Color Light yellow to yellow
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SMILES
O=C(C1=CC2=C(C=NC=C2)C=C1)NC3=CC=C(C)C(C(NC4=CN=C(NC5=CC=CC(NC6CCN(C(/C=C/CN(C)C)=O)CC6)=C5)N=C4)=O)=C3
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선적
Room temperature in continental US; may vary elsewhere.
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보관
Powder -20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month
용액&용해도
DMSO : 100 mg/mL (146.24 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
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.
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.
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Select the appropriate dissolution method based on your experimental animal and administration route.
- For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
- To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for In Vivo experiments, it is recommended to prepare freshly and use it on the same day.
- 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.
Add each solvent one by one: 10% DMSO 40% PEG300 5% Tween-80 45% Saline
Solubility: ≥ 2.08 mg/mL (3.04 mM); Clear solution
This protocol yields a clear solution of ≥ 2.08 mg/mL (saturation unknown).
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (20.8 mg/mL) to 400 μL PEG300, and mix evenly; then add 50 μL Tween-80 and mix evenly; then add 450 μL Saline to adjust the volume to 1 mL.
Preparation of Saline: Dissolve 0.9 g sodium chloride in ddH₂O and dilute to 100 mL to obtain a clear Saline solution.
Please enter the basic information of animal experiments:
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-
-
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Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Please enter your animal formula composition:
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%DMSO +
Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak.
-
%+
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+%Tween-80 + +
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%Saline +
The co-solvents required include: DMSO, . All of co-solvents are available by MedChemExpress (MCE). , Tween 80. All of co-solvents are available by MedChemExpress (MCE).
Working solution concentration: 0.22 mg/mL
Method for preparing stock solution: mg drug dissolved in μL DMSO. Stock solution concentration: mg/mL.
1. Take μL DMSO stock solution;
2. Add μL .
μL , mix evenly;
3. Then add μL Tween 80, mix evenly;
4. Then add μL
Please ensure that the stock solution in the first step is dissolved to a clear state, and add co-solvents in sequence. You can use ultrasonic heating (ultrasonic cleaner, recommended frequency 20-40 kHz), vortexing, etc. to assist dissolution.
순도&문서
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Data Sheet (267 KB)
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SDS (251 KB)
- English - EN (251 KB)
- Français - FR (251 KB)
- Deutsch - DE (251 KB)
- Norwegian - NO (251 KB)
- Español - ES (251 KB)
- Swedish - SV (251 KB)
- Italian - IT (251 KB)
- Korean - KR (251 KB)
- Portuguese - PT (251 KB)
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Handling Instructions (2659 KB)
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 mM | 1.4624 mL | 7.3121 mL | 14.6242 mL | 36.5604 mL |
| 5 mM | 0.2925 mL | 1.4624 mL | 2.9248 mL | 7.3121 mL | |
| 10 mM | 0.1462 mL | 0.7312 mL | 1.4624 mL | 3.6560 mL | |
| 15 mM | 0.0975 mL | 0.4875 mL | 0.9749 mL | 2.4374 mL | |
| 20 mM | 0.0731 mL | 0.3656 mL | 0.7312 mL | 1.8280 mL | |
| 25 mM | 0.0585 mL | 0.2925 mL | 0.5850 mL | 1.4624 mL | |
| 30 mM | 0.0487 mL | 0.2437 mL | 0.4875 mL | 1.2187 mL | |
| 40 mM | 0.0366 mL | 0.1828 mL | 0.3656 mL | 0.9140 mL | |
| 50 mM | 0.0292 mL | 0.1462 mL | 0.2925 mL | 0.7312 mL | |
| 60 mM | 0.0244 mL | 0.1219 mL | 0.2437 mL | 0.6093 mL | |
| 80 mM | 0.0183 mL | 0.0914 mL | 0.1828 mL | 0.4570 mL | |
| 100 mM | 0.0146 mL | 0.0731 mL | 0.1462 mL | 0.3656 mL |