ORIC-944 free base · Synonyms: Rinzimetostat
ORIC-944 is a selective, orally active, allosteric inhibitor targeting the EED subunit of polycomb repressive complex 2 (PRC2).
For research use only. Not for human or veterinary use.
ORIC-944 structure
CAS No.: 2369769-29-7
Pack sizes & pricing
| Size | Price | SKU | Stock | |
|---|---|---|---|---|
| 100 mg | USD 550.00 | BP-00084-100mg | In stock | Get quote |
| 250 mg | USD 850.00 | BP-00084-250mg | In stock | Get quote |
| 500 mg | USD 1,350.00 | BP-00084-500mg | In stock | Get quote |
| 1 g | USD 1,900.00 | BP-00084-1g | In stock | Get quote |
| 5 g | Inquire | BP-00084-5g | In stock | Inquire |
| 10 g | Inquire | BP-00084-10g | In stock | Inquire |
Description
ORIC-944 is a selective, orally active, allosteric inhibitor targeting the EED subunit of polycomb repressive complex 2 (PRC2). ORIC-944 is synergistic with androgen receptor pathway inhibitors (ARPIs) for the study of metastatic prostate cancer.
Biological activity
In Vivo Rinzimetostat (ORIC-944) (30, 100, 200 mg/kg; op; everyday for 50 days) induces significantly tumor regressions at all dose levels tested. Rinzimetostat (ORIC-944) (30 mg/kg; op; everyday for 30 days) demonstrates strong single agent activity to enzalutamide in prostate cancer xenograft model.
Specifications
- MW (average)
- 456.5147
- Formula
- C26H25FN6O
- CAS No.
- 2369769-29-7
- Physical state
- Solid
- Color
- white to off-white
- Shipping
- Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
- Storage
- Powder 4℃ 2 years; In solvent -20℃ 1 month;
Solubility
Soluble in DMSO
- In vitro
- DMSO : 100 mg/mL
Documents
References
Same target
Search Histone MethyltransferaseSame research area
Search Cancer- BP-00006 SLF Exclusive free base · >98%
- BP-00008 NSC-339004 free base · >98%
- BP-00019 SLF-amido-C2-COOH free base · >98%
- BP-00020 PT262 free base · >98%
- BP-00022 Inolitazone free base · >98%
- BP-00024 KX2-361 free base · >98%
- BP-00030 EML4-ALK kinase inhibitor 1 free base · >98%
- BP-00037 SB 328437 free base · >98%