| Identification | Back Directory | [Name]
SUBSTANCE P | [CAS]
33507-63-0 | [Synonyms]
Sub
Aids114081
RPKPQFFGLM
SUBSTANCE P
Aids-114081
P substance
Neurokinin P
RPKPQQFFGLM-NH2
substance P (SP)
SUBSTANCE P AMIDE
SUBSTANCE P (TYR8)
SUBSTANCE P BOVINE
Substance P Acetate
Substance P TFA salt
SUBSTANCE P (HUMAN, BOVINE, RAT, MOUSE)
SUBSTANCE P, F & D VERSION OF S6883*ACET ATE
SUBSTANCE P, [D-ARG1, D-PRO2, D-TRP7,9, LEU11]
ARG-PRO-LYS-PRO-GLN-GLN-PHE-PHE-GLY-LEU-MET-NH2
H2N-ARG-PRO-LYS-PRO-GLN-GLN-PHE-PHE-GLY-LEU-MET
H-ARG-PRO-LYS-PRO-GLN-GLN-PHE-PHE-GLY-LEU-MET-NH2
H-Arg-Pro-Lys-Pro-Gln-Gln-Phe-Phe-Gly-Leu-Met-NH2 acetate salt
L-Arg-L-Pro-L-Lys-L-Pro-L-Gln-L-Gln-L-Phe-L-Phe-Gly-L-Leu-Met-NH2
L-Arg-L-Pro-L-Lys-L-Pro-L-Gln-L-Gln-L-Phe-L-Phe-Gly-L-Leu-L-Met-NH2
L-Arg-L-Pro-L-Lys-L-Pro-L-Glu(NH2)-L-Glu(NH2)-L-Phe-L-Phe-Gly-L-Leu-L-Met-NH2
(S)-N1-((5S,8S,14S,17S,20S)-23-aMino-14,17-dibenzyl-5-carbaMoyl-8-isobutyl-7,10,13,16,19,23-hexaoxo-2-thia-6,9,12,15,18-pentaazatricosan-20-yl)-2-((S)-1-((S)-6-aMino-2-((S)-1-((S)-2-aMino-5-guanidinopentanoyl)pyrrolidine-2-carboxaMido)hexanoyl)pyrrolidine
(2S)-2-[[(2S)-1-[(2S)-6-amino-2-[[(2S)-1-[(2S)-2-amino-5-(diaminomethylideneamino)pentanoyl]pyrrolidine-2-carbonyl]amino]hexanoyl]pyrrolidine-2-carbonyl]amino]-N-[(2S)-5-amino-1-[[(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]amino]-1,5-dioxopentan-2-yl]pentanediamide | [EINECS(EC#)]
251-545-8 | [Molecular Formula]
C63H98N18O13S | [MDL Number]
MFCD00076780 | [MOL File]
33507-63-0.mol | [Molecular Weight]
1347.63 |
| Chemical Properties | Back Directory | [Melting point ]
148 °C | [density ]
1.42±0.1 g/cm3(Predicted) | [storage temp. ]
−20°C
| [solubility ]
H2O: 1 mg/mL
| [form ]
powder
| [pka]
13.26±0.46(Predicted) | [color ]
white
| [Water Solubility ]
Soluble in water, DMSO, and Acetic Acid. | [Sequence]
H-Arg-Pro-Lys-Pro-Gln-Gln-Phe-Phe-Gly-Leu-Met-NH2 | [Cosmetics Ingredients Functions]
SKIN CONDITIONING - EMOLLIENT
SKIN PROTECTING | [InChIKey]
ADNPLDHMAVUMIW-UHFFFAOYSA-N |
| Hazard Information | Back Directory | [Chemical Properties]
White freeze-dried powder, easily soluble in water. High-purity aqueous solution is easily inactivated. Adding Tween 80, gelatin, human plasma albumin or bovine immunoglobulin G can increase its stability. It is unstable when the pH is greater than 8 and is inactivated by pepsin and chymotrypsin. It should be stored at a low pH value and filled with nitrogen or added with antioxidants to avoid its inactivation. | [Uses]
Substance P is a neurokinin undecapeptide neurotransmitter and neuromodulator. | [Definition]
ChEBI: Substance P is a neuropeptide consisting of 11-amino acids. It preferentially activates neurokinin-1 receptors, exterting excitatory effects on central and peripheral neurons and involved in pain transmission. It has a role as a neurotransmitter, a vasodilator agent and a neurokinin-1 receptor agonist. It is a conjugate base of a substance P(3+). | [General Description]
Substance P is a polypeptide consisting of 11 amino acidresidues. It has been implicated in the transmission of“painful” sensory information through the spinal cord tohigher centers in the central nervous system. Substance Pis localized in the primary afferent sensory fibers. Other pharmacologicaleffects are vasodilatation, stimulation of smoothmuscles, stimulation of salivary secretion, and diuresis. In addition,this neuropeptide contributes to some inflammatory responses.Approximately 50% of the known neuropeptides aresynthesized as biologically inactive glycine extended precursorsthat require a carboxy-terminal posttranslational amidationfor biological activity. Amidation enzymes are responsiblefor the conversion of the carboxyl group of the neuropeptide tothe corresponding amide group and include the two amidatingenzymes peptidylglycine α-monooxygenase (PAM) and peptidylamidoglycolatelyase (PGL), which work sequentially toproduce the inflammatory neuropeptide Substance P from aninactive precursor peptide. Much research is being performedto exploit this mechanism of inflammation. | [Biological Activity]
Cell permeable: no''Primary Target
Substance P receptors''Product does not compete with ATP.''Reversible: no | [storage]
-20°C |
|
| Company Name: |
Combio (Suzhou) Ltd. Gold
|
| Telephone: |
17751201929; 17751201929 |
| Website: |
http://www.combiosz.com/ |
| Company Name: |
J & K SCIENTIFIC LTD.
|
| Telephone: |
18210857532 18210857532 |
| Website: |
https://www.jkchemical.com |
| Company Name: |
Sigma-Aldrich
|
| Telephone: |
021-61415566 800-8193336 |
| Website: |
https://www.sigmaaldrich.cn |
|