ChemWhat Code: 1480783 Identification Physical Data Spectra Route of Synthesis (ROS) Safety and Hazards Other Data Identification Product Name Fragment-[9-31]-Semaglutide Molecular Structure CAS Registry Number N/A EINECS Number MDL Number Beilstein Registry Number Synonyms (2S,5S,8S,11S,14S,17S,20S,26S,29S,32S,35S,62R)-35-(((6S,12S,15S,18S,21S,24S,27S,30S,33S)-21-((1H-indol-3-yl)methyl)-1-amino-30-benzyl-27-((S)-sec-butyl)-35-carboxy-6-((carboxymethyl)carbamoyl)-12-(3-guanidinopropyl)-1-imino-18-isobutyl-15-isopropyl-24-methyl-8,11,14,17,20,23,26,29,32-nonaoxo-2,7,10,13,16,19,22,25,28,31-decaazapentatriacontan-33-yl)carbamoyl)-2-amino-26-(3-amino-3-oxopropyl)-20-(2-carboxyethyl)-14-(4-hydroxybenzyl)-8,11-bis(hydroxymethyl)-17-isobutyl-5-isopropyl-29,32-dimethyl-3,6,9,12,15,18,21,24,27,30,33,41,50,59,64-pentadecaoxo-43,46,52,55-tetraoxa-4,7,10,13,16,19,22,25,28,31,34,40,49,58,63-pentadecaazaoctacontane-1,62,80-tricarboxylic acid Molecular Formula C150H239N35O46 Molecular Weight 3268.8 InChI InChI Key Canonical SMILES N[C@@H](CC(O)=O)C(N[C@@H](C(C)C)C(N[C@@H](CO)C(N[C@@H](CO)C(N[C@@H](CC1=CC=C(O)C=C1)C(N[C@@H](CC(C)C)C(N[C@@H](CCC(O)=O)C(NCC(N[C@@H](CCC(N)=O)C(N[C@@H](C)C(N[C@@H](C)C(N[C@@H](CCCCNC(COCCOCCNC(COCCOCCNC(CC[C@H](C(O)=O)NC(CCCCCCCCCCCCCCCCC(O)=O)=O)=O)=O)=O)C(N[C@@H](CCC(O)=O)C(N[C@@H](CC2=CC=CC=C2)C(N[C@@H]([C@@H](C)CC)C(N[C@@H](C)C(N[C@@H](CC3=CNC4=C3C=CC=C4)C(N[C@@H](CC(C)C)C(N[C@@H](C(C)C)C(N[C@@H](CCCNC(N)=N)C(NCC(N[C@@H](CCCNC(N)=N)C(NCC(O)=O)=O)=O)=O)=O)=O)=O)=O)=O)=O)=O)=O)=O)=O)=O)=O)=O)=O)=O)=O)=O)=O)=O Physical Data Appearance No data available Solubility No data available Flash Point No data available Refractive index No data available Sensitivity No data available Melting Point No data available Spectra No data available Route of Synthesis (ROS) No data available Safety and Hazards No data available Other Data HS Code 382290 Storage At room temperature and away from light Related Chemicals Use Pattern Fragment-[9-31]-Semaglutide is chemically (2S,5S,8S,11S,14S,17S,20S,26S,29S,32S,35S,62R)-35-(((6S,12S,15S,18S,21S,24S,27S,30S,33S)-21-((1H-indol-3-yl)methyl)-1-amino-30-benzyl-27-((S)-sec-butyl)-35-carboxy-6-((carboxymethyl)carbamoyl)-12-(3-guanidinopropyl)-1-imino-18-isobutyl-15-isopropyl-24-methyl-8,11,14,17,20,23,26,29,32-nonaoxo-2,7,10,13,16,19,22,25,28,31-decaazapentatriacontan-33-yl)carbamoyl)-2-amino-26-(3-amino-3-oxopropyl)-20-(2-carboxyethyl)-14-(4-hydroxybenzyl)-8,11-bis(hydroxymethyl)-17-isobutyl-5-isopropyl-29,32-dimethyl-3,6,9,12,15,18,21,24,27,30,33,41,50,59,64-pentadecaoxo-43,46,52,55-tetraoxa-4,7,10,13,16,19,22,25,28,31,34,40,49,58,63-pentadecaazaoctacontane-1,62,80-tricarboxylic acid

Pratt, Ronald G
The notable result of significant inhibition of viral expression by 89.78% and enhanced defensive mechanism against crop viruses were observed [190]
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The pituitary gland is responsible for releasing this hormone