Quinazoline, 4-[1-[(2-bromophenyl)methyl]-2-phenyl-1H-indol-3-yl]-7-methoxy-6-[3-(4-morpholinyl)propoxy]-
![Quinazoline, 4-[1-[(2-bromophenyl)methyl]-2-phenyl-1H-indol-3-yl]-7-methoxy-6-[3-(4-morpholinyl)propoxy]- Structure](CAS/20210305/GIF/2470908-79-1.gif)
- CAS No.
- 2470908-79-1
- Chemical Name:
- Quinazoline, 4-[1-[(2-bromophenyl)methyl]-2-phenyl-1H-indol-3-yl]-7-methoxy-6-[3-(4-morpholinyl)propoxy]-
- Synonyms
- YS-370;YS370,YS 370;4-(3-((4-(1-(2-Bromobenzyl)-2-phenyl-1H-indol-3-yl)-7-methoxyquinazolin-6-yl)oxy)propyl)morpholine;Quinazoline, 4-[1-[(2-bromophenyl)methyl]-2-phenyl-1H-indol-3-yl]-7-methoxy-6-[3-(4-morpholinyl)propoxy]-
- CBNumber:
- CB511140017
- Molecular Formula:
- C37H35BrN4O3
- Molecular Weight:
- 663.6
- MDL Number:
- MOL File:
- 2470908-79-1.mol
Quinazoline, 4-[1-[(2-bromophenyl)methyl]-2-phenyl-1H-indol-3-yl]-7-methoxy-6-[3-(4-morpholinyl)propoxy]- Properties
| Boiling point | 784.8±60.0 °C(Predicted) |
|---|---|
| Density | 1.35±0.1 g/cm3(Predicted) |
| storage temp. | Store at -20°C |
| solubility | DMSO : 8.33 mg/mL (12.55 mM; ultrasonic and warming and heat to 80°C) |
| form | Solid |
| pka | 7.00±0.10(Predicted) |
| color | White to off-white |
Quinazoline, 4-[1-[(2-bromophenyl)methyl]-2-phenyl-1H-indol-3-yl]-7-methoxy-6-[3-(4-morpholinyl)propoxy]- Chemical Properties,Uses,Production
Uses
YS-370 (compound 44) is a potent, high selective, and orally active inhibitor of P-glycoprotein (P-gp). YS-370 stimulates the P-gp ATPase activity and has moderate inhibition against CYP3A4. YS-370 effectively reverses multidrug resistance (MDR) to paclitaxel and colchicine in SW620/AD300 and HEK293T-ABCB1 cells. YS-370 in combination with paclitaxel achieves much stronger antitumor activity[1].
Biological Activity
YS-370 (compound 44) is a potent, high selective, and orally active inhibitor of P-glycoprotein (P-gp). YS-370 stimulates the P-gp ATPase activity and has moderate inhibition against CYP3A4. YS-370 effectively reverses multidrug resistance (MDR) to paclitaxel and colchicine in SW620/AD300 and HEK293T-ABCB1 cells. YS-370 in combination with paclitaxel achieves much stronger antitumor activity[1].
References
[1]. Yuan S, et al. Discovery of New 4-Indolyl Quinazoline Derivatives as Highly Potent and Orally Bioavailable P-Glycoprotein Inhibitors. J Med Chem. 2021;64(19):14895-14911.
Quinazoline, 4-[1-[(2-bromophenyl)methyl]-2-phenyl-1H-indol-3-yl]-7-methoxy-6-[3-(4-morpholinyl)propoxy]- Preparation Products And Raw materials
Raw materials
Preparation Products
Quinazoline, 4-[1-[(2-bromophenyl)methyl]-2-phenyl-1H-indol-3-yl]-7-methoxy-6-[3-(4-morpholinyl)propoxy]- Suppliers
| Supplier | Tel | Country | ProdList | Advantage | |
|---|---|---|---|---|---|
| TargetMol Chemicals Inc. | +1-781-999-5354; +17819995354 | marketing@targetmol.com | United States | 32432 | 58 |
| Shanghai Chaolan Chemical Technology Center | 021-QQ：65489617 15618227136 | Sales@ATKchemical.com | China | 9848 | 58 |
| Absin Bioscience Inc. | 021-38015121 18438616290 | lanwu@univ-bio.com | China | 24731 | 58 |
| Bide Pharmatech Ltd. | 400-1647117 13681763483 | product02@bidepharm.com | China | 62320 | 58 |
| TargetMol Chemicals Inc. | 4008200310 | marketing@tsbiochem.com | China | 24989 | 58 |
| Suzhou Zhixin Biotechnology Co., Ltd. | 0512-65118909 18100677375 | sales@szzxbio.com | China | 3000 | 58 |
| Shanghai Yifei Biotechnology Co. , Ltd. | 021-65675885 18964387627 | customer_service@efebio.com | China | 11973 | 58 |
| RD International Technology Co., Limited | 18024082417 | market@ubiochem.com | China | 9835 | 58 |
| Sangon Biotech (Shanghai) Co.,Ltd. | 400-821-026 | Sales@sangon.com | China | 6710 | 58 |
