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Growth hormone-release inhibiting factor; treatment of severe, acute hemorrhage of gastroduodenal ulcers; experimental antidiabetic.
Ala-Gly-Cys-Lys-Asn-Phe-Phe-Trp-Lys-Thr-Phe-Thr-Ser-Cys
somatostatin
| Conditions | Yield |
|---|---|
|
With
iodine; acetic acid;
In
methanol; water;
at 20 ℃;
for 2h;
|
68% |
|
With
hydrogenchloride; potassium platinum(IV) tetracyanochloride;
In
water;
for 1h;
Ambient temperature;
|
|
|
With
TentaGel resin supported platinum(IV) complex;
at 25 ℃;
|
|
|
With
hydrogenchloride; trans-[Pt(1,10-phenanthroline)(ethylenediamine)Cl2]Cl2;
In
water;
at 20 ℃;
Reagent/catalyst;
Catalytic behavior;
|
|
|
With
Pt(1,2-diaminoethane)2Br4;
In
water; trifluoroacetic acid;
at 20 ℃;
for 0.0166667h;
Solvent;
|
C178H268N18O29S2
somatostatin
| Conditions | Yield |
|---|---|
|
With
chlorotriisopropylsilane; trifluoroacetic acid;
In
water;
|
95% |
The CAS number of 15-28-Somatostatin-28 is 38916-34-6.
More information of 15-28-Somatostatin-28 38916-34-6 are:
|
CAS Number |
38916-34-6 |
|
Density |
1.43 g/cm3 |
|
Boiling Point |
1970.9 °C at 760 mmHg |
|
Flash Point |
1145.7 °C |
|
Vapor Pressure |
0mmHg at 25°C |
|
Refractive Index |
1.669 |
|
PSA |
663.83000 |
|
LogP |
2.28620 |
|
Pka |
2.94±0.70(Predicted) |
Synonyms for 15-28-Somatostatin-28 38916-34-6:Somatostatin, cyclic;Somatostatina;
The chemical formula of 15-28-Somatostatin-28 is C76H104N18O19S2 which containing 76 Carbon atoms,104 Hydrogen atoms,18 Nitrogen atoms,19 Oxygen atoms and 2 Sulfur atoms,and the molecular weight of 15-28-Somatostatin-28 is 1637.9.
15-28-Somatostatin-28, also known as Somatostatin, is a peptide hormone derived from the larger precursor molecule, somatostatin-14. It is a cyclic peptide consisting of 14 amino acid residues, including a disulfide bridge between two cysteine residues at positions 3 and 14. This peptide hormone is known for its various physiological functions, such as inhibiting the release of growth hormone and regulating the secretion of insulin and glucagon. It is typically found as a white powder and has been studied for its potential therapeutic applications.
InChI:InChI=1/C76H104N18O19S2/c1-41(79)64(100)82-37-61(99)83-58-39-114-115-40-59(76(112)113)92-72(108)57(38-95)91-75(111)63(43(3)97)94-71(107)54(33-46-23-11-6-12-24-46)90-74(110)62(42(2)96)93-66(102)51(28-16-18-30-78)84-69(105)55(34-47-36-81-49-26-14-13-25-48(47)49)88-68(104)53(32-45-21-9-5-10-22-45)86-67(103)52(31-44-19-7-4-8-20-44)87-70(106)56(35-60(80)98)89-65(101)50(85-73(58)109)27-15-17-29-77/h4-14,19-26,36,41-43,50-59,62-63,81,95-97H,15-18,27-35,37-40,77-79H2,1-3H3,(H2,80,98)(H,82,100)(H,83,99)(H,84,105)(H,85,109)(H,86,103)(H,87,106)(H,88,104)(H,89,101)(H,90,110)(H,91,111)(H,92,108)(H,93,102)(H,94,107)(H,112,113)
Relevant articles related to 15-28-Somatostatin-28:
|
Article |
Source |
|
Formation of peptide disulfide bonds through a trans-dibromido-Pt(IV) complex oxidation reaction: Kinetic and mechanistic analyses |
Ma, Dongying,Song, Changying,Sun, Jingjing,Shen, Shigang,Huo, Shuying , (2021/01/18) |
|
A study to develop platinum(iv) complex chemistry for peptide disulfide bond formation |
Huo, Shuying,Shen, Shigang,Song, Changying,Sun, Jingjing,Zhao, Xiaowei supporting information, p. 1736 - 1741 (2020/02/20) |
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