Splenopentin

Base Information

Chemical Name:Splenopentin
CAS No.:75957-60-7
Molecular Formula:C₃₁H₅₁N₉O₉
Molecular Weight:693.801
Hs Code.:
DSSTox Substance ID:DTXSID50997315
Nikkaji Number:J366.269A

Synonyms:Arg-Lys-Glu-Val-Tyr;splenin pentapeptide (32-36);splenopentin;thymopoietin III pentapeptide (32-36)

Suppliers and Price of Splenopentin

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

Usbiological
Splenopentin
1mg
$ 531.00

Sigma-Aldrich
ANTI-SP5(C-TERMINAL) antibody produced in rabbit purified immunoglobulin, buffered aqueous solution
400 μL
$ 389.00

Sigma-Aldrich
ANTI-SP5(C-TERMINAL) antibody produced in rabbit purified immunoglobulin, buffered aqueous solution
400ul
$ 361.00

American Custom Chemicals Corporation
ARG-LYS-GLU-VAL-TYR 95.00%
25MG
$ 818.61

American Custom Chemicals Corporation
ARG-LYS-GLU-VAL-TYR 95.00%
5MG
$ 642.87

Total 12 raw suppliers

Chemical Property of Splenopentin

Chemical Property:

PKA:3.07±0.10(Predicted)
PSA：90.18000
Density:1.42 g/cm³
LogP:1.93530
Storage Temp.:-15°C
XLogP3:-6
Hydrogen Bond Donor Count:11
Hydrogen Bond Acceptor Count:12
Rotatable Bond Count:23
Exact Mass:693.38097424
Heavy Atom Count:49
Complexity:1130

Purity/Quality:

99% ^*data from raw suppliers

Splenopentin ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)C(C(=O)NC(CC1=CC=C(C=C1)O)C(=O)O)NC(=O)C(CCC(=O)O)NC(=O)C(CCCCN)NC(=O)C(CCCN=C(N)N)N
Isomeric SMILES:CC(C)[C@@H](C(=O)N[C@@H](CC1=CC=C(C=C1)O)C(=O)O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)N

Technology Process of Splenopentin

There total 3 articles about Splenopentin 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:

: 75957-67-4
Z-Arg(NO₂)-Lys(Z)-Glu(OBzl)-Val-Tyr-OBzl

: 75957-60-7
Arg-Lys-Glu-Val-Tyr

Guidance literature:: With methyl-phenyl-thioether; hydrogen fluoride; methoxybenzene; ortho-cresol; for 0.5h; ice-bath;
DOI:10.1248/cpb.28.2507

Reference yield:

: 2304-98-5
N₅-[imino(nitroamino)methyl]-N₂-[(phenylmethoxy)carbonyl]-L-ornithine

: 75957-60-7
Arg-Lys-Glu-Val-Tyr

Guidance literature:: Multi-step reaction with 2 steps

1: Et₃N, N-hydroxybenzotriazole, watersoluble carbodiimide / 18 h / 0 °C

2: HF, anisole-thioanisole-o-cresol / 0.5 h / ice-bath

With methyl-phenyl-thioether; watersoluble carbodiimide; hydrogen fluoride; benzotriazol-1-ol; methoxybenzene; ortho-cresol; triethylamine;
DOI:10.1248/cpb.28.2507