Agtad[cfwkyc]V

Base Information

Chemical Name:Agtad[cfwkyc]V
CAS No.:9047-55-6
Molecular Formula:C62H84 N14 O17 S2
Molecular Weight:1361.54
Hs Code.:
ChEMBL ID:CHEMBL1163463
DSSTox Substance ID:DTXSID701027163
Mol file:9047-55-6.mol

Synonyms:AGTAD[CFWKYC]V;Urotensin II, teleost fish;CHEMBL1163463;Urotensin II (Gillichthys mirabilis);DTXSID701027163;HY-P3957;BDBM50320454;NCGC00167193-01;CS-0634424

Suppliers and Price of Agtad[cfwkyc]V

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

American Custom Chemicals Corporation
UROTENSIN II, FROG 95.00%
5MG
$ 498.36

Alfa Aesar
Urotensin II goby
10mg
$ 408.00

Alfa Aesar
Urotensin II goby
5mg
$ 268.00

Total 8 raw suppliers

Chemical Property of Agtad[cfwkyc]V

Chemical Property:

PSA：553.59000
LogP:2.74280
XLogP3:-5
Hydrogen Bond Donor Count:18
Hydrogen Bond Acceptor Count:21
Rotatable Bond Count:27
Exact Mass:1360.55802961
Heavy Atom Count:95
Complexity:2650

Purity/Quality:

99% ^*data from raw suppliers

UROTENSIN II, FROG 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)C(C(=O)O)NC(=O)C1CSSCC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N1)CC2=CC=C(C=C2)O)CCCCN)CC3=CNC4=CC=CC=C43)CC5=CC=CC=C5)NC(=O)C(CC(=O)O)NC(=O)C(C)NC(=O)C(C(C)O)NC(=O)CNC(=O)C(C)N
Isomeric SMILES:C[C@H]([C@@H](C(=O)N[C@@H](C)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@H]1CSSC[C@H](NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@@H](NC1=O)CC2=CC=CC=C2)CC3=CNC4=CC=CC=C43)CCCCN)CC5=CC=C(C=C5)O)C(=O)N[C@@H](C(C)C)C(=O)O)NC(=O)CNC(=O)[C@H](C)N)O

Technology Process of Agtad[cfwkyc]V

There total 3 articles about Agtad[cfwkyc]V 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: 52.0%

: 112332-51-1
Z-Ala-Gly-Thr-Ala-Asp(OBzl)-Cys<*>-Phe-Trp(Mts)-Lys(Z)-Cys<*>-Val-OBzl

: 9047-55-6
[125I]-Urotensin II (Gillichthys mirabilis)

Guidance literature:: With trimethylsilyl trifluoromethanesulfonate; diphenyl sulfide; 3-methyl-phenol; In trifluoroacetic acid; for 2h;
DOI:10.1248/cpb.35.2339

Reference yield: 16.0%

: 81657-27-4
Z-Ala-Gly-Thr-Ala-Asp(OBzl)-Cys(MBzl)-Phe-Trp-Lys(Z)-Tyr-Cys(MBzl)-Val-OBzl

: 9047-55-6
urotensin II, human

Guidance literature:: With ethylenediaminetetraacetic acid; trifluorormethanesulfonic acid; methyl-phenyl-thioether; In trifluoroacetic acid; for 1.5h;
DOI:10.1248/cpb.30.349

Reference yield:

: Cys(S-acetamidomethyl)-urotensin II

: 9047-55-6
[125I]-Urotensin II (Gillichthys mirabilis)

Guidance literature:: With hydrogenchloride; silver trifluoromethanesulfonate; methoxybenzene; Multistep reaction; 1.) TFA, 4 deg C, 1.5 h, 2.) DMSO, r.t., 7 h;
DOI:10.1016/S0040-4039(00)74049-4