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H-ASP-TYR-D-TRP-VAL-D-TRP-D-TRP-LYS-NH2

H-ASP-TYR-D-TRP-VAL-D-TRP-D-TRP-LYS-NH2 Structure
H-ASP-TYR-D-TRP-VAL-D-TRP-D-TRP-LYS-NH2
  • CAS No.135306-85-3
  • Chemical Name:H-ASP-TYR-D-TRP-VAL-D-TRP-D-TRP-LYS-NH2
  • CBNumber:CB5297135
  • Molecular Formula:C57H68N12O10
  • Formula Weight:1081.22
  • MOL File:135306-85-3.mol
H-ASP-TYR-D-TRP-VAL-D-TRP-D-TRP-LYS-NH2 Property
  • Boiling point 1555.4±65.0 °C(Predicted)
  • Density 1.361±0.06 g/cm3(Predicted)
  • storage temp. -20°C
  • solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
  • form solid
  • pka 3.71±0.10(Predicted)
  • color white
  • UNSPSC Code 51111800
  • NACRES NA.32
Safety
  • WGK Germany  :3
Hazard and Precautionary Statements (GHS)
  • Symbol(GHS)
  • Signal word
  • Hazard statements
  • Precautionary statements
H-ASP-TYR-D-TRP-VAL-D-TRP-D-TRP-LYS-NH2 Price More Price(1)
  • Brand: Sigma-Aldrich(India)
  • Product number: M157
  • Product name : MEN-10,376
  • Purity: ≥95% (HPLC), solid
  • Packaging: 500μG
  • Price: ₹41968.53
  • Updated: 2022/06/14
  • Buy: Buy

H-ASP-TYR-D-TRP-VAL-D-TRP-D-TRP-LYS-NH2 Chemical Properties,Usage,Production

  • Uses MEN10376 is a neurokinin 2 (NK2) receptor antagonist.
  • Biochem/physiol Actions Potent and selective NK-2 tachykinin receptor antagonist.
  • in vivo

    Men 10376 (1 and 3 μmol/kg) antagonizes increase in bladder motility produced by the NK-2 receptor agonist in rats[2].

H-ASP-TYR-D-TRP-VAL-D-TRP-D-TRP-LYS-NH2 Preparation Products And Raw materials
Raw materials
Preparation Products
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H-ASP-TYR-D-TRP-VAL-D-TRP-D-TRP-LYS-NH2 Spectrum
135306-85-3, H-ASP-TYR-D-TRP-VAL-D-TRP-D-TRP-LYS-NH2Related Search:
  • Peptide
  • Tachykinin receptor
  • Tachykinins
  • Peptides for Cell Biology
  • Neuropeptides
  • AntagonistPeptides for Cell Biology
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  • Amino Acids and Peptides
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  • Antagonist
  • Tachykinins
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  • C57H68N12O10
  • 化合物 MEN 10376
  • MEN 10376肽
  • 135306-85-3
  • (Tyr?,D-Trp?·?·?,Lys-NH???)-Neurokinin A (4-10)
  • (Tyr5,D-Trp6.8.9,Lys-NH?1?)-Neurokinin A (4-10)
  • 3-amino-4-[[1-[[1-[[1-[[1-[[1-[(1,6-diamino-1-oxohexan-2-yl)amino]-3-(1H-indol-3-yl)-1-oxopropan-2-yl]amino]-3-(1H-indol-3-yl)-1-oxopropan-2-yl]amino]-3-methyl-1-oxobutan-2-yl]amino]-3-(1H-indol-3-yl)-1-oxopropan-2-yl]amino]-3-(4-hydroxyphenyl)-1-oxopropan-2-yl]amino]-4-oxobutanoic acid
  • L-Lysinamide, L-α-aspartyl-L-tyrosyl-D-tryptophyl-L-valyl-D-tryptophyl-D-tryptophyl-
  • (Tyr5,D-Trp6.8.9,Lys-NH21?)-Neurokinin A (4-10)
  • Neurokinin-2 receptor antagonist
  • MEN-10,376, ≥95% (HPLC)
  • MEN-10,376 , ≥95% (HPLC)
  • 3-amino-4-[[1-[[1-[[1-[[1-[[1-[(1,6-diamino-1-oxohexan-2-yl)amino]-3-(1H-indol-3-yl)-1-oxopropan-2-yl]amino]-3-(1H-indol-3-yl)-1-oxopropan-2-yl]amino]-3-methyl-1-oxobutan-2-yl]amino]-3-(1H-indol-3-yl)-1-oxopropan-2-yl]amino]-3-(4-hydroxyphenyl)-1-oxopropa
  • L-alpha-Aspartyl-L-tyrosyl-D-tryptophyl-L-valyl-D-tryptophyl-D-tryptophyl-L-lysinamide
  • MEN-10,376 ≥95%
  • (Tyr5,D-Trp6·8·9,Lys-NH210)-Neurokinin A (4-10) MEN 10376
  • L-Asp-L-Tyr-D-Trp-L-Val-D-Trp-D-Trp-L-Lys-NH2
  • M.W. 1081.24 C57H68N12O10
  • alpha-neurokinin, fragment 4-10, [Tyr5, Trp6,8,9, Lys10]
  • L-Lysinamide, L-a-aspartyl-L-tyrosyl-D-tryptophyl-L-valyl-D-tryptophyl-D-tryptophyl-
  • neurokinin A(4-10), Tyr(5)-Trp(6,8,9)-Lys(10)-
  • [TYR5 ,D -TRP6,8 9 ,LYS10 ]-ALPHA-NEUROKININ A FRAGMENT 4-10 97%
  • MEN-10,376 SYNTHETIC >95% NK2 TACHYKININ RECEPT
  • (tyr5,D-trp6,8,9,lys10)-A-neurokinin*fragment 4-1
  • tyr(5)-trp(6,8,9)-lys(10)-neurokinina(4-10
  • (TYR5,D-TRP6,8,9,LYS-NH(2/10))-NEUROKININ A (4-10)
  • [TYR5, D-TRP6,8,9, LYS10]NEUROKININ A (4-10)
  • [TYR5,D-TRP6,8 9,LYS10]-ALPHA-NEUROKININ A FRAGMENT 4-10
  • ASP-TYR-D-TRP-VAL-D-TRP-D-TRP-LYS-NH2
  • H-ASP-TYR-D-TRP-VAL-D-TRP-D-TRP-LYS-NH2
  • MEN 10376