- ACY-1215
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- $0.00 / 25kg
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2024-04-12
- CAS:1316214-52-4
- Min. Order: 1kg
- Purity: 99%
- Supply Ability: 2000ton
- ACY-1215
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- $0.00 / 1KG
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2022-10-14
- CAS:1316214-52-4
- Min. Order: 1KG
- Purity: 98%
- Supply Ability: 1Ton
- ACY-1215
-
- $0.00 / 1g
-
2022-04-19
- CAS:1316214-52-4
- Min. Order: 1g
- Purity: 98%
- Supply Ability: 10 grams
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| | ACY-1215 Basic information |
| Product Name: | ACY-1215 | | Synonyms: | Rocilinostat (ACY-1215);2-(Diphenylamino)-N-[7-(hydroxyamino)-7-oxoheptyl]-5-pyrimidinecarboxamide;ACY 63;2-(DiphenylaMino)-N-(7-(hydroxyaMino)-7-oxoheptyl)pyriMidine-5-carboxaMide;Rocilinostat, >=99%;5-Pyrimidinecarboxamide, 2-(diphenylamino)-N-[7-(hydroxyamino)-7-oxoheptyl]-;2-(Diphenylamino)-N-[7-(hydroxyamino)-7-oxoheptyl]-5-pyrimidinecarboxamide ACY 1215;Ricolinostat | | CAS: | 1316214-52-4 | | MF: | C24H27N5O3 | | MW: | 433.5 | | EINECS: | | | Product Categories: | Inhibitors;Inhibitor | | Mol File: | 1316214-52-4.mol |  |
| | ACY-1215 Chemical Properties |
| Melting point | 189 - 191°C | | density | 1.239±0.06 g/cm3(Predicted) | | storage temp. | -20°C Freezer | | solubility | DMSO (Slightly), Methanol (Slightly) | | pka | 9.47±0.20(Predicted) | | form | Solid | | color | White to Off-White |
| | ACY-1215 Usage And Synthesis |
| Description | ACY-1215 is an inhibitor of histone deacetylase 6 (HDAC6; IC50 = 5 nM). It is at least 10-fold less active against other HDACs in enzymatic assays. ACY-1215 shows synergistic activity with the proteasome inhibitor bortezomib against multiple myeloma (MM) cells, inducing protracted endoplasmic reticulum stress and apoptosis. ACY-1215 combined with proteasome inhibitors suppresses tumor growth and increases survival in mice with MM and mantle cell lymphoma xenografts. A multicenter phase I trial examining ACY-1215 combined with the E3 ligase inhibitor lenalidomide and dexamethasone in multiple myeloma found inhibition of HDAC6 in vivo. ACY-1215 also diminishes liver cyst development and fibrosis in a rat model of polycystic liver disease. | | Uses | This compound acts as a selective HDAC-6 (histone deacetylase) inihibitor. HDAC is linked to the transcription of DNA in cancers, including multiple myeloma (MM). | | Definition | ChEBI: N-[7-(hydroxyamino)-7-oxoheptyl]-2-(N-phenylanilino)-5-pyrimidinecarboxamide is a pyrimidinecarboxylic acid. | | target | HDAC6 |
| | ACY-1215 Preparation Products And Raw materials |
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