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| Cas No.: | 1613373-33-3 |
| Chemical Name: | PCO371 |
| Synonyms: | PCO371;TE53TU0WSQ;1-(3,5-dimethyl-4-(2-((4-oxo-2-(4-(trifluoromethoxy)phenyl)-1,3,8-triazaspiro[4.5]dec-1-en-8-yl)sulfonyl)ethyl)phenyl)-5,5-dimethylimidazolidine-2,4-dione;1-[3,5-dimethyl-4-[2-[[4-oxo-2-[4-(trifluoromethoxy)phenyl]-1,3,8-triazaspiro[4.5]dec-1-en-8-yl]sulfonyl]ethyl]phenyl]-5,5-dimethylimidazolidine-2,4-dione;US9428505, Compound 7;BDBM64562;BCP31012;DB14946;SB19668;CS-0;2,4-Imidazolidinedione, 1-(3,5-dimethyl-4-(2-((4-oxo-2-(4-(trifluoromethoxy)phenyl)-1,3,8-triazaspir |
| SMILES: | S(CCC1C(C)=CC(=CC=1C)N1C(NC(C1(C)C)=O)=O)(N1CCC2(C(NC(C3C=CC(=CC=3)OC(F)(F)F)=N2)=O)CC1)(=O)=O |
| Formula: | C29H32F3N5O6S |
| M.Wt: | 635.654496192932 |
| Purity: | >98% |
| Sotrage: | 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO |
| Description: | PCO371 is a novel, orally active small molecule that acts as a full agonist of PTHR1. PCO371 does not affect the PTH type 2 receptor (PTHR2), and analysis using PTHR1-PTHR2 chimeric receptors indicated that Proline 415 of PTHR1 is critical for PCO371-mediated PTHR1 activation. Oral administration of PCO371 to osteopenic rats provokes a significant increase in bone turnover with limited increase in bone mass. In hypocalcemic rats, PCO371 restores serum calcium levels without increasing urinary calcium, and with stronger and longer-lasting effects than PTH injections. These results strongly suggest that PCO371 can provide a new treatment option for PTH-related disorders, including hypoparathyroidism. |
MSDS
COA
| LOT NO. | DOWNLOAD |
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| 2018-0101 |
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