| Company Name: |
Absin Bioscience Inc.
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| Tel: |
13761418683 |
| Email: |
fengmj@univ-bio.com |
| Products Intro: |
Cas:1505453-59-7
ProductName:BET bromodomain inhibitor
Purity: 98% | Package: 2mg;5mg;10mg;25mg
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| Company Name: |
|
| Tel: |
|
| Email: |
info@bocsci.com |
| Products Intro: |
Cas:1505453-59-7
ProductName:BET bromodomain inhibitor
Purity: >=98% | CustNote: Reach out to us for more information about custom solutions.
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| Company Name: |
Shanghai jerryxing Biomedical Technology Co., Ltd
|
| Tel: |
17521512546 17721492509 |
| Email: |
460170712@qq.com |
| Products Intro: |
Cas:1380087-89-7
ProductName:CPI 0610; CPI0610; BET bromodomain inhibitor
Purity: 98% HPLC | Package: 500mg;1g;10g;100g;1kg
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Bet Bromodomain Inhibitor manufacturers
- MT1 BET inhibitor
-
- $5.00
-
2026-09-15
- CAS:2060573-82-0
- Min. Order: 1BOX
- Purity: 99.99%
- Supply Ability: 100000000
- MT1 BET inhibitor
-
- $5.00
-
2026-09-15
- CAS:2060573-82-0
- Min. Order: 1BOX
- Purity: 99.99%
- Supply Ability: 100000000
|
| | Bet Bromodomain Inhibitor Basic information |
| Product Name: | Bet Bromodomain Inhibitor | | Synonyms: | (4S)-6-(4-Chlorophenyl)-1-methyl-4H-isoxazolo[5,4-d][2]benzazepine-4-acetamide;CPI0160;2-[6-(4-Chloro-phenyl)-1-Methyl-4H-3-oxa-2,5-diaza-benzo[e]azulen-4-yl]-acetaMide;2-((4S)-6-(4-chlorophenyl)-1-methyl-4H-benzo[c]isoxazolo[4,5-e]azepin-4-yl)acetamide;4H-Isoxazolo[5,4-d][2]benzazepine-4-acetamide, 6-(4-chlorophenyl)-1-methyl-, (4S)-;0610;Pelabresib (CPI-0610);CP1-0610 | | CAS: | 1380087-89-7 | | MF: | C20H16ClN3O2 | | MW: | 365.81 | | EINECS: | | | Product Categories: | Inhibitors | | Mol File: | 1380087-89-7.mol |  |
| | Bet Bromodomain Inhibitor Chemical Properties |
| Boiling point | 622.8±55.0 °C(Predicted) | | density | 1.41±0.1 g/cm3(Predicted) | | storage temp. | Store at -20°C | | solubility | DMSO : 100 mg/mL (273.37 mM; Need ultrasonic) | | form | Powder | | pka | 16.07±0.40(Predicted) | | color | White to off-white | | InChI | InChI=1S/C20H16ClN3O2/c1-11-18-14-4-2-3-5-15(14)19(12-6-8-13(21)9-7-12)23-16(10-17(22)25)20(18)26-24-11/h2-9,16H,10H2,1H3,(H2,22,25)/t16-/m0/s1 | | InChIKey | GCWIQUVXWZWCLE-INIZCTEOSA-N | | SMILES | N1=C(C2=CC=C(Cl)C=C2)C2=CC=CC=C2C2C(C)=NOC=2[C@@H]1CC(N)=O |
| | Bet Bromodomain Inhibitor Usage And Synthesis |
| Uses | BET Bromodomain Inhibitor has be shown to inhibit myeloma cell proliferation in clinically relevant models. | | in vivo | Pelabresib (30-60 mg/kg; oral administration; for 28 days; MV-4-11 mouse xenograft model) treatment results in substantial suppression of tumor growth over the time period examined (41%, 80%, and 74% tumor growth inhibition, respectively), without any significant body weight loss in the animals[1]. | Animal Model: | MV-4-11 mouse xenograft model[1] | | Dosage: | 30 mg/kg once daily, 30 mg/kg twice daily, or 60 mg/kg once daily | | Administration: | Oral administration; for 28 days | | Result: | Suppressed of tumor growth, without any significant body weight loss in the animals.
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| | IC 50 | BRD4-BD1: 39 nM (IC50) |
| | Bet Bromodomain Inhibitor Preparation Products And Raw materials |
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