Urotensin II(Gillichthys mirabilis reduced) (9CI)

Base Information

Chemical Name:Urotensin II(Gillichthys mirabilis reduced) (9CI)
CAS No.:81643-78-9
Molecular Formula:C₆₂H₈₆N₁₄O₁₇S₂
Molecular Weight:1363.58
Hs Code.:

Synonyms:1: PN:US20040121343 PAGE: 31 unclaimed sequence; 31: PN: WO0031265 FIGURE: 6unclaimed sequence; 35: PN: WO2004045592 SEQID: 35 unclaimed sequence; 3: PN:US6159700 SEQID: 3 claimed sequence; 6: PN: WO0114888 SEQID: 4 unclaimedsequence; 77: PN: US20090175821 SEQID: 99 claimed protein; 7: PN: US20050255484SEQID: 7 unclaimed sequence; 7: PN: WO2004037863 SEQID: 6 claimed sequence; 96:PN: WO0069900 SEQID: 99 unclaimed sequence; L-Valine,N-[N-[N-[N2-[N-[N-[N-[N-[N-[N-(N-L-alanylglycyl)-L-threonyl]-L-alanyl]-L-a-aspartyl]-L-cysteinyl]-L-phenylalanyl]-L-tryptophyl]-L-lysyl]-L-tyrosyl]-L-cysteinyl]-

Suppliers and Price of Urotensin II(Gillichthys mirabilis reduced) (9CI)

Supply Marketing:

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

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Chemical Property of Urotensin II(Gillichthys mirabilis reduced) (9CI)

Chemical Property:

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Safty Information:

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MSDS Files:: SDS file from LookChem

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Technology Process of Urotensin II(Gillichthys mirabilis reduced) (9CI)

There total 1 articles about Urotensin II(Gillichthys mirabilis reduced) (9CI) 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:

: 111193-51-2
Z-Ala-Gly-Thr-Ala-Asp(OBzl)-Cys(MBzl)-Phe-Trp(Mts)-Lys(Z)-Tyr-Cys(MBzl)-Val-OBzl

: 81643-78-9
urotensin II

Guidance literature:: With trimethylsilyl trifluoromethanesulfonate; diphenyl sulfide; 3-methyl-phenol; methoxybenzene; thallium(III) trifluoroacetate; Yield given. Multistep reaction; 1.) TFA, 60 min, 2.) TFA, 120 min, 0 deg C;
DOI:10.1248/cpb.35.2339