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491851-53-7

491851-53-7 Structure

491851-53-7 Structure
IdentificationBack Directory
[Name]

HEMOKININ 1 (HUMAN)
[CAS]

491851-53-7
[Synonyms]

HHK-1
HK-1 (HUMAN)
HEK-1 (HUMAN)
HEMOKININ 1 (HUMAN)
HK-1 (huMan), HEK-1 (huMan)
Hemokinin 1 human >=98% (HPLC), solid
Hemokinin 1 (human) trifluoroacetate salt
THR-GLY-LYS-ALA-SER-GLN-PHE-PHE-GLY-LEU-MET-NH2
HeMokinin 1 (huMan) HK-1 (huMan), HEK-1 (huMan)
H-THR-GLY-LYS-ALA-SER-GLN-PHE-PHE-GLY-LEU-MET-NH2
L-Methioninamide, L-threonylglycyl-L-lysyl-L-alanyl-L-seryl-L-glutaminyl-L-phenylalanyl-L-phenylalanylglycyl-L-leucyl-
(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-6-amino-2-[[2-[[(2S,3R)-2-amino-3-hydroxybutanoyl]amino]acetyl]amino]hexanoyl]amino]propanoyl]amino]-3-hydroxypropanoyl]amino]-N-[(2S)-1-[[(2S)-1-[[2-[[(2S)-1-[[(2S)-1-amino-4-methylsulfanyl-1-oxobutan-2-yl]amino]-4-methyl-1-oxopentan-2-yl]amino]-2-oxoethyl]amino]-1-oxo-3-phenylpropan-2-yl]amino]-1-oxo-3-phenylpropan-2-yl]pentanediamide
[Molecular Formula]

C54H84N14O14S
[MDL Number]

MFCD06656083
[MOL File]

491851-53-7.mol
[Molecular Weight]

1185.4
Chemical PropertiesBack Directory
[storage temp. ]

−20°C
[solubility ]

Water: soluble
[form ]

solid
[color ]

white
[Water Solubility ]

Soluble to 0.70 mg/ml in water
[Sequence]

H-Thr-Gly-Lys-Ala-Ser-Gln-Phe-Phe-Gly-Leu-Met-NH2
[InChIKey]

NYBLUYYRUFKGTB-XJCFQSCISA-N
Safety DataBack Directory
[Safety Statements ]

22-24/25
[WGK Germany ]

3
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Uses]

Hemokinin 1, human is a selective tachykinin neurokinin 1 (NK1) receptor full agonist. Hemokinin 1, human is a full agonist at NK2 and NK3 receptor. Hemokinin 1, human can produces an opioid-independent analgesia[1][2].
[Biological Activity]

Hemokinin 1 (HK1) is an endogenous agonist for all tachykinin receptors. Howeverit is highly selective for the NK1 (neurokinin 1) receptor. HK1 and substance-P compete with each other for binding to NK1. HK1 is involved in the B-cell as well as T-cell development.''NK1 tachykinin receptor agonist.
[IC 50]

NK1; NK2; NK3
[References]

[1] Cai-Yun Fu, et al. Hemokinin-1(4-11)-induced analgesia selectively up-regulates δ-opioid receptor expression in mice. PLoS One DOI:10.1371/journal.pone.0090446
[2] Francesca Bellucci, et al. Pharmacological profile of the novel mammalian tachykinin, hemokinin 1. Br J Pharmacol. 2002 Jan;135(1):266-74. DOI:10.1038/sj.bjp.0704443
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