Substance P acetate salt hydrate

SIGMA/S6883 - ≥95% (HPLC), powder

CAS Number: 137348-11-9 (anhydrous)
Empirical Formula (Hill Notation): C₆₃H₉₈N₁₈O₁₃S · xC₂H₄O₂ · yH₂O
Molecular Weight: 1347.63 (anhydrous free base basis)
Linear Formula: C₆₃H₉₈N₁₈O₁₃S · xC₂H₄O₂ · yH₂O
Product Type: Chemical

Catalog Number	PKG Qty.	Price	Quantity


45-S6883-.5MG	0.5 mg	$56.00 1/EA		Add To Favorites
45-S6883-1MG	1 mg	$95.80 1/EA		Add To Favorites
45-S6883-5MG	5 mg	$420.00 1/EA		Add To Favorites
45-S6883-10MG	10 mg	$478.00 1/EA		Add To Favorites
45-S6883-25MG	25 mg	$1070.00 1/EA		Add To Favorites

Properties
Descriptions
Safety Info.
Basic Data

assay	≥95% (HPLC)
color	white
form	powder
InChI	1S/C63H98N18O13S.C2H4O2.H2O/c1-37(2)33-45(57(89)74-41(53(68)85)27-32-95-3)73-52(84)36-72-54(86)46(34-38-15-6-4-7-16-38)78-58(90)47(35-39-17-8-5-9-18-39)79-56(88)42(23-25-50(66)82)75-55(87)43(24-26-51(67)83)76-59(91)49-22-14-31-81(49)62(94)44(20-10-11-28-64)77-60(92)48-21-13-30-80(48)61(93)40(65)19-12-29-71-63(69)70;1-2(3)4;/h4-9,15-18,37,40-49H,10-14,19-36,64-65H2,1-3H3,(H2,66,82)(H2,67,83)(H2,68,85)(H,72,86)(H,73,84)(H,74,89)(H,75,87)(H,76,91)(H,77,92)(H,78,90)(H,79,88)(H4,69,70,71);1H3,(H,3,4);1H2/t40-,41-,42-,43-,44-,45-,46?,47-,48-,49-;;/m0../s1
InChI key	VHKFRLDSEZYWAC-CIYRQLMPSA-N
mol wt	1348 Da by calculation (Average Mass)
Quality Level	200
SMILES string	[H]O[H].CC(O)=O.CSCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)CNC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H]3CCCN3C(=O)[C@H](CCCCN)NC(=O)[C@@H]4CCCN4C(=O)[C@@H](N)CCCNC(N)=N)C(N)=O
solubility	0.1 M acetic acid: 1 mg/mL
storage condition	(Keep container tightly closed in a dry and well-ventilated place.)
storage temp.	−20°C
UniProt accession no.	P20366

Amino Acid Sequence:	Arg-Pro-Lys-Pro-Gln-Gln-Phe-Phe-Gly-Leu-Met-NH2
Application:	Substance P acetate salt hydrate has been: • used as a neurokinin 1 (NK1) receptor agonist for the activation of spinal nociceptive circuitry in mice • administered in central nucleus (ACE) in rat to study its positive reinforcing effects • used in competition binding assays • used as an inhibitor of myosin light chain kinase in isolated lymphatic vessels from rat
Biochem/physiol Actions:	NK-1 agonist; potent vasodilator and hypotensive agent.
Biochem/physiol Actions:	NK-1 agonist; potent vasodilator and hypotensive agent; induces salivation; increases capillary permeability; induces mast cell degranulation; putative neurotransmitter in sensory (pain) afferents.
Biochem/physiol Actions:	Substance P has proinflammatory effects on epithelial and immune cells. It has been associated with inflammatory diseases related to gastrointestinal and respiratory systems. Substance P modulates contractility of smooth muscles, transport of ions in the epithelium, vascular permeability and immune functions in the gut.
General description:	Research area: Cell Signaling Substance P is a member of the tachykinin family of peptides. It is encoded by the tachykinin precursor 1 (TAC1) gene mapped to human chromosome 7q21-q22. Substance P is a small peptide produced by macrophages, lymphocytes, eosinophils, dendritic cells and nerves. It is part of the neurokinin group.

RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point(F)	Not applicable
Flash Point(C)	Not applicable

Purity	≥95% (HPLC)
Storage Temp.	−20°C
UNSPSC	12352200

Choose a favorite list for this item:

Catalog Number	Description	Price

		$

Please choose a list :

Continue Shopping

Returns/Order support

Please fill out the form below if you want to request order support from Krackeler Scientific.