Company Name: |
Daicel Chiral Technologies (China)CO.,LTD
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Tel: |
021-50460086-9 15921403865 |
Email: |
han_yajun@dctc.daicel.com |
Products Intro: |
Product Name:Edoxaban-D6 CAS:1304701-57-2 Purity:95% HPLC Package:10mg ;25mg;50mg;100mg Remarks:DCTI-A-219
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Company Name: |
Clearsynth Canada Inc.
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Tel: |
+1.415.685.4395 |
Email: |
enquiry@clearsynth.com |
Products Intro: |
Product Name:Edoxaban D6 CAS:1304701-57-2 Remarks:CS-O-11960
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Company Name: |
Shanghai Han-Xiang Chemical Co., Ltd.
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Tel: |
15971444841 |
Email: |
amber@biochempartner.com |
Products Intro: |
Product Name:Edoxaban-d6 CAS:1304701-57-2 Purity:98% HPLC LCMS Package:100G;1KG
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Company Name: |
Jinan blalong chemical co. LTD
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Tel: |
2710913286@.com |
Email: |
1513643261@qq.com |
Products Intro: |
Product Name:Edoxaban-d6 CAS:1304701-57-2 Purity:99% HPLC Package:50G;10G;1G;500MG;100MG
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| Edoxaban-d6 Basic information |
Product Name: | Edoxaban-d6 | Synonyms: | Edoxaban-d6;N-[(1S,2R,4S)-4-[bis(trideuteriomethyl)carbamoyl]-2-[(5-methyl-6,7-dihydro-4H-[1,3]thiazolo[5,4-c]pyridine-2-carbonyl)amino]cyclohexyl]-N'-(5-chloropyridin-2-yl)oxamide;[2H6]-Edoxaban;Edoxaban hydrochloride salt;2H6]-Edoxaban hydrochloride salt | CAS: | 1304701-57-2 | MF: | C24H30ClN7O4S | MW: | 548.06 | EINECS: | | Product Categories: | | Mol File: | 1304701-57-2.mol | ![Edoxaban-d6 Structure](CAS/20211123/GIF/1304701-57-2.gif) |
| Edoxaban-d6 Chemical Properties |
Melting point | >205°C (dec.) | storage temp. | Hygroscopic, Refrigerator, under inert atmosphere | solubility | Chloroform (Slightly), Dichloromethane (Slightly) | form | Solid | color | Pale Orange to Pale Red | Stability: | Hygroscopic |
| Edoxaban-d6 Usage And Synthesis |
Description | Edoxaban-d6 is intended for use as an internal standard for the quantification of edoxaban by GC- or LC-MS. Edoxaban is an orally bioavailable and potent inhibitor of factor Xa (Kis = 0.561 and 0.903 nM for free and complexed human factor Xa, respectively). It is >10,000-fold selective for factor Xa over thrombin, FVIIa/sTF, FXIa, tPA, aPC, trypsin, plasmin, and chymotrypsin. Edoxaban prolongs prothrombin, activated partial thromboplastin, and thrombin clotting times in a concentration-dependent manner ex vivo in human plasma. Oral administration of edoxaban (0.5-12.5 mg/kg) reduces thrombus formation and prolongs prothrombin time in a dose-dependent manner in rat and rabbit models of venous stasis thrombosis. It also reduces thrombus formation in a rat model of platinum wire-induced venous thrombosis. Formulations containing edoxaban have been used to prevent stroke in patients with atrial fibrillation. | Uses | Edoxaban-d6 is the isotope labelled analog of Edoxaban (E555520); an anticoagulant drug which acts as a direct factor Xa inhibitor. |
| Edoxaban-d6 Preparation Products And Raw materials |
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