Goralatide

Base Information

Chemical Name:Goralatide
CAS No.:120081-14-3
Molecular Formula:C₂₀H₃₃N₅O₉
Molecular Weight:487.51
Hs Code.:
Mol file:120081-14-3.mol

Synonyms:L-Proline,1-[N2-[N-(N-acetyl-L-seryl)-L-a-aspartyl]-L-lysyl]-; 1-[N2-[N-(N-Acetyl-L-seryl)-L-a-aspartyl]-L-lysyl]-L-proline;150: PN: US20090175821 PAGE: 404 claimed protein; 74: PN: WO2009151689 PAGE: 16claimed protein; Acetyl-N-Ser-Asp-Lys-Pro; Goralatide;N-Acetyl-seryl-aspartyl-lysyl-proline; Seraspenide

Suppliers and Price of Goralatide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Biosynth Carbosynth
Ac-S-D-K-P
25 mg
$ 768.00

Biosynth Carbosynth
Ac-S-D-K-P
10 mg
$ 384.00

Biosynth Carbosynth
Ac-S-D-K-P
5 mg
$ 226.00

Biosynth Carbosynth
Ac-S-D-K-P
2 mg
$ 113.00

Biosynth Carbosynth
Ac-S-D-K-P
1 mg
$ 65.00

AK Scientific
Goralatide
25mg
$ 1086.00

Total 4 raw suppliers

Chemical Property of Goralatide

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Boiling Point:992°Cat760mmHg
PKA:3.39±0.20(Predicted)
Flash Point:553.7°C
PSA：228.46000
Density:1.382g/cm³
LogP:-1.05680

Purity/Quality:

99%, ^*data from raw suppliers

Ac-S-D-K-P ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of Goralatide

There total 10 articles about Goralatide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 65.0%

: C₃₇H₆₅N₅O₁₁

: 120081-14-3
Ac-SDKP

Guidance literature:: With trifluoroacetic acid; In dichloromethane; for 2h;
DOI:10.1021/op0202179

Reference yield:

: C₂₈H₅₀N₄O₈

: 120081-14-3
Ac-SDKP

Guidance literature:: Multi-step reaction with 4 steps

1: dicyclohexyl-carbodiimide / dichloromethane / 1 h

2: 4-Aminomethylpiperidine / dichloromethane / 1 h

3: triethylamine / dichloromethane / 1 h

4: trifluoroacetic acid / dichloromethane / 2 h

With 4-Aminomethylpiperidine; triethylamine; dicyclohexyl-carbodiimide; trifluoroacetic acid; In dichloromethane;
DOI:10.1021/op0202179

Reference yield:

: C₅₀H₇₃N₅O₁₂

: 120081-14-3
Ac-SDKP

Guidance literature:: Multi-step reaction with 3 steps

1: 4-Aminomethylpiperidine / dichloromethane / 1 h

2: triethylamine / dichloromethane / 1 h

3: trifluoroacetic acid / dichloromethane / 2 h

With 4-Aminomethylpiperidine; triethylamine; trifluoroacetic acid; In dichloromethane;
DOI:10.1021/op0202179