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Ac-[Tyr1,D-Phe2]-GRF (1-29) amide (human)
CAS No. 93965-89-0
Ac-[Tyr1,D-Phe2]-GRF (1-29) amide (human)( ——— )
Catalog No. M41195 CAS No. 93965-89-0
[Ac-Tyr1,D-Phe2]GRF 1-29, amide (human), a growth hormone releasing factor (GRF) analogue, is a vasoactive intestinal peptide (VIP) antagonist.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
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Biological Information
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Product NameAc-[Tyr1,D-Phe2]-GRF (1-29) amide (human)
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NoteResearch use only, not for human use.
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Brief Description[Ac-Tyr1,D-Phe2]GRF 1-29, amide (human), a growth hormone releasing factor (GRF) analogue, is a vasoactive intestinal peptide (VIP) antagonist.
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Description[Ac-Tyr1,D-Phe2]GRF 1-29, amide (human), a growth hormone releasing factor (GRF) analogue, is a vasoactive intestinal peptide (VIP) antagonist.
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In VitroCell Proliferation Assay Cell Line:C6 rat glioblastoma cells Concentration:0.1 pM-10 nM Incubation Time:3 days Result:Induced a dose-dependent cell proliferation increase.
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In Vivo———
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Synonyms———
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PathwayOthers
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TargetOther Targets
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RecptorVIP
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Research Area———
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Indication———
Chemical Information
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CAS Number93965-89-0
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Formula Weight3476.09
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Molecular FormulaC157H252N44O43S
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Purity>98% (HPLC)
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Solubility———
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SMILES———
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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Heneicosanoic acid
Heneicosanoic acid (HEA) is a fatty acid found in human milk fat. HEA is also a part of the phospholipids of the articular cartilage boundary lubricant. HEA is a constituent of red blood cell fatty acids.
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Picropodophyllotoxin
Picropodophyllin is a cyclolignan alkaloid found in the mayapple plant family (Podophyllum peltatum), and a small molecule inhibitor of the insulin-like growth factor 1 receptor (IGF1R) with potential antineoplastic activity.
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ELA-21 (human)
High affinity apelin receptor agonist. Binds apelin receptors in left ventricle from normal and pulmonary arterial hypertensive (PAH) hearts (pKi values are 9.31 and 9.46, respectively). Bioactive fragment of ELA-32. Inhibits forskolin-induced cAMP production and stimulates β-arrestin recruitment in vitro.
