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208041-90-1

208041-90-1 Structure

208041-90-1 Structure
IdentificationBack Directory
[Name]

H-ARG-SER-ARG-THR-ARG-GLN-PHE-TYR-GLY-LEU-MET-NH2
[CAS]

208041-90-1
[Synonyms]

HK-1, MOUSE
HEMOKININ-1
HEK-1, MOUSE
HK-1 (MOUSE, RAT)
HEK-1 (MOUSE, RAT)
HEMOKININ 1 (MOUSE)
H2N-RSRTRQFYGLM-AMIDE
HEMOKININ 1 MOUSE?, >98%
HEMOKININ 1 (MOUSE, RAT)
Hemokinin 1 mouse,RSRTRQFYGLM, >98%
HK-1 (Mouse, rat), HEK-1 (Mouse, rat)
ARG-SER-ARG-THR-ARG-GLN-PHE-TYR-GLY-LEU-MET-NH2
H-ARG-SER-ARG-THR-ARG-GLN-PHE-TYR-GLY-LEU-MET-NH2
HeMokinin 1 (Mouse, rat) HK-1 (Mouse, rat), HEK-1 (Mouse, rat)
TACHYKININ 4 PRECURSOR (56-66) AMIDE [RATTUS NORVEGICUS]/[MUS MUSCULUS]
L-Methioninamide, L-arginyl-L-seryl-L-arginyl-L-threonyl-L-arginyl-L-glutaminyl-L-phenylalanyl-L-tyrosylglycyl-L-leucyl-
[Molecular Formula]

C61H100N22O15S
[MDL Number]

MFCD06659096
[MOL File]

208041-90-1.mol
[Molecular Weight]

1413.65
Chemical PropertiesBack Directory
[density ]

1.48±0.1 g/cm3(Predicted)
[storage temp. ]

−20°C
[solubility ]

H2O: soluble
[form ]

powder
[pka]

9.82±0.15(Predicted)
[color ]

white
[Water Solubility ]

Soluble to 2 mg/ml in water
Safety DataBack Directory
[Safety Statements ]

22-24/25
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

Hemokinin 1 (mouse) is a selective agonist of neurokinin-1 receptor, with Ki of 0.175 nM and 560 nM for human NK1 receptor and human NK2 receptor, respectively.
[in vivo]

Hemokinin 1 (mouse) (0.01-100 nmol/kg i.v., n=10) induces a dose-related hypotension that is maximal at the dose of 10 nmol/kg. For systolic blood pressure (SBP), the ED50 value is 0.2 nmol/kg (0.1-0.4 nmol/kg) for Hemokinin 1 (mouse). For diastolic blood pressure (DBP), the ED50 value is 0.1 nmol/kg (0.07-0.2 nmol/kg) for Hemokinin 1 (mouse). Hemokinin 1 (mouse) (0.1-100 nmol/kg, i.v.) induces a dose-related salivary secretion in atropine-pretreated rats[1].

[IC 50]

NK1
[storage]

Store at -20°C
[References]

[1] Francesca Bellucci, et al. Pharmacological profile of the novel mammalian tachykinin, hemokinin 1. Br J Pharmacol. 2002 Jan; 135(1): 266-274
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