| Company Name: |
Suzhou Zhixin Biotechnology Co., Ltd.
|
| Tel: |
0512-65118909 18100677375 |
| Email: |
sales@szzxbio.com |
| Products Intro: |
Product Name:Sinbaglustat
CAS:441061-33-2
Purity:98%+ Package:1g;10g;100g
|
| Company Name: |
Shanghai Yifei Biotechnology Co. , Ltd.
|
| Tel: |
021-65675885 18964387627 |
| Email: |
customer_service@efebio.com |
| Products Intro: |
Product Name:OGT2378
CAS:441061-33-2
Purity:99.00% Package:1mg;5mg;10mg
|
| Company Name: |
TargetMol Chemicals Inc.
|
| Tel: |
15002134094 |
| Email: |
marketing@targetmol.cn |
| Products Intro: |
Product Name:Sinbaglustat
CAS:441061-33-2
Purity:99.93% Package:1mg/RMB 1190;5mg/RMB 2980;10mg/RMB 4390
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OGT2378 manufacturers
- Sinbaglustat
-
- $66.00 / 1mg
-
2025-11-09
- CAS:441061-33-2
- Min. Order:
- Purity: 99.93%
- Supply Ability: 10g
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| | OGT2378 Basic information |
| Product Name: | OGT2378 | | Synonyms: | OGT2378;ACT-519276;Sinbaglustat;3,4,5-Piperidinetriol, 2-(hydroxymethyl)-1-pentyl-, (2S,3R,4R,5S)-;Sinbaglustat, 10 mM in DMSO | | CAS: | 441061-33-2 | | MF: | C11H23NO4 | | MW: | 233.3 | | EINECS: | | | Product Categories: | | | Mol File: | 441061-33-2.mol |  |
| | OGT2378 Chemical Properties |
| Boiling point | 405.5±45.0 °C(Predicted) | | density | 1.201±0.06 g/cm3(Predicted) | | pka | 13.71±0.70(Predicted) | | form | Solid | | color | Light yellow to yellow |
| | OGT2378 Usage And Synthesis |
| Uses | Sinbaglustat (OGT2378) is a dual inhibitor of glucosylceramide synthase (GCS) and non-lysosomal glucosyl ceramidase (GBA2). Sinbaglustat is an orally available N-alkyl iminosugar that crosses the blood-brain barrier. Sinbaglustat can be used for the research of central neurodegenerative diseases associated with lysosomal dysfunctions[1][2]. | | in vivo | Sinbaglustat (OGT2378; administered p.o., in the powdered chow, at a dose of 2500 mg/kg/day, corresponding to 35-40 mg of Sinbaglustat per mouse per day) is highly effective in impeding melanoma tumor growth?in vivo. The effectiveness of p.o. Sinbaglustat in this murine model suggests that inhibition of glycosphingolipid synthesis is a promising approach to inhibit tumor progression[1]. | Animal Model: | Female syngeneic C57BL/6 mice, 6-8 weeks old bearing MEB4 melanoma tumor[1] | | Dosage: | 35-40 mg per mouse per day | | Administration: | Administered p.o., in the powdered chow, at a dose of 2500 mg/kg/day | | Result: | Inhibited MEB4 melanoma tumor growth in a syngeneic, orthotopic murine model.
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| | References | [1] Michael Weiss,?et al. Inhibition of melanoma tumor growth by a novel inhibitor of glucosylceramide synthase. Cancer Res.?2003 Jul 1;63(13):3654-8. PMID:12839955
[2] Martine Gehin,?et al. Assessment of Target Engagement in a First-in-Human Trial with Sinbaglustat, an Iminosugar to Treat Lysosomal Storage Disorders. Clin Transl Sci.?2021 Mar;14(2):558-567. DOI:10.1111/cts.12911 |
| | OGT2378 Preparation Products And Raw materials |
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