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Home > Products > API Active Pharmaceutical Ingredient > Somalutide Intermediate GLP-1 Analogue CAS 910463-68-2 with Molecular Formula C187H291N45O59 and Molecular Weight 4113.580 for Long term Storage -20 ± 5℃

Somalutide Intermediate GLP-1 Analogue CAS 910463-68-2 with Molecular Formula C187H291N45O59 and Molecular Weight 4113.580 for Long term Storage -20 ± 5℃

Product Details

Place of Origin: China

Brand Name: Sunshine

Certification: COA,ISO

Model Number: 910463-68-2

Payment & Shipping Terms

Minimum Order Quantity: Negotiation

Price: Negotiation

Packaging Details: Aluminum Foil Bag, Drum

Delivery Time: 7-15 working days

Payment Terms: T/T,L/C,D/A,Western Union

Supply Ability: 1Ton/Month

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CAS 910463-68-2 API ingredient

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Active Pharmaceutical Ingredient CAS 910463-68-2

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Pharmaceutical API with CAS 910463-68-2

CAS NO::
910463-68-2
Appearance::
White Powder
Molecular Formula::
C187H291N45O59
Molecular Weight::
4113.580
EINECS NO::
691-729-9
MDL NO::
NA
CAS NO::
910463-68-2
Appearance::
White Powder
Molecular Formula::
C187H291N45O59
Molecular Weight::
4113.580
EINECS NO::
691-729-9
MDL NO::
NA
Somalutide Intermediate GLP-1 Analogue CAS 910463-68-2 with Molecular Formula C187H291N45O59 and Molecular Weight 4113.580 for Long term Storage -20 ± 5℃
CAS 910463-68-2
Product Description
Product Name: CAS NO: 910463-68-2
Chemical & Physical Properties
Appearance: White powder
Assay: ≥99.0%
Long term Storage: -20 ± 5℃

We can provide GMP/DMF file support for this product, as well as other different standards to meet your specific requirements.

Available Somalutide Intermediates
CAS NO. Chemical name
910463-68-2 GLP-1 analogue
1662688-20-1 Fmoc-L-Lys[Oct-(otBu)-Glu-(otBu)-AEEA-AEEA]-OH
1446013-07-5 Fmoc-His-Aib-OH
1169630-40-3 Ste-Glu-AEEA-AEEA-OSU
1118767-16-0 tBuO-Ste-Glu(AEEA-AEEA-OH)-OtBu
1169630-82-3 Semaglutide intermediate P29
203787-91-1 Salcaprozate Sodium
Available Fillers for Semaglutide Production
  • SP FOCUROSE FF
  • DEAE FOCUROSE FF
  • Silica C8

This product is a long-acting dosage form developed based on the basic structure of liraglutide, demonstrating enhanced efficacy in the treatment of type 2 diabetes. As a new generation GLP-1 (glucagon-like peptide-1) analogue developed by Novo Nordisk, Denmark, it represents an advancement in diabetes treatment options.

Novo Nordisk has completed six Phase IIIa studies and submitted a new drug registration application to the U.S. Food and Drug Administration (FDA) on December 5, 2016 for weekly administration of somalutide. A marketing authorisation application (MAA) has also been submitted to the European Medicines Agency (EMA). Somalutide is currently in Phase III clinical trials for a once-daily oral formulation.

Products under patent are offered for R&D purposes only. The final responsibility for use lies exclusively with the buyer.
For product inquiries or additional information, please contact our team.