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SUBSTANCE P

SUBSTANCE P Structure
CAS No.
33507-63-0
Chemical Name:
SUBSTANCE P
Synonyms
Sub;TYR8;RPKPQFFGLM;Aids114081;SUBSTANCE P;P substance;Aids-114081;Neurokinin P;RPKPQQFFGLM-NH2;substance P (SP)
CBNumber:
CB4114260
Molecular Formula:
C63H98N18O13S
Molecular Weight:
1347.63
MOL File:
33507-63-0.mol
Modify Date:
2024/4/19 20:05:26

SUBSTANCE P Properties

Melting point 148 °C
Density 1.42±0.1 g/cm3(Predicted)
storage temp. −20°C
solubility H2O: 1 mg/mL
pka 13.26±0.46(Predicted)
form powder
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
InChIKey ADNPLDHMAVUMIW-UHFFFAOYSA-N

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H312-H332-H302
Precautionary statements  P280-P302+P352-P312-P322-P363-P501-P261-P271-P304+P340-P312-P264-P270-P301+P312-P330-P501
WGK Germany  3
3-10-21

SUBSTANCE P price More Price(3)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 05-23-0600 Substance P - CAS 33507-63-0 - Calbiochem Neuropeptide found in high concentrations in the gut. 33507-63-0 1MG ₹5810 2022-06-14 Buy
Sigma-Aldrich(India) 05-23-0600 Substance P - CAS 33507-63-0 - Calbiochem Neuropeptide found in high concentrations in the gut. 33507-63-0 5MG ₹18830 2022-06-14 Buy
Sigma-Aldrich(India) 05-23-0600 Substance P - CAS 33507-63-0 - Calbiochem Neuropeptide found in high concentrations in the gut. 33507-63-0 25MG ₹41350 2022-06-14 Buy
Product number Packaging Price Buy
05-23-0600 1MG ₹5810 Buy
05-23-0600 5MG ₹18830 Buy
05-23-0600 25MG ₹41350 Buy

SUBSTANCE P Chemical Properties,Uses,Production

Uses

Substance P is a neurokinin undecapeptide neurotransmitter and neuromodulator.

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.

SUBSTANCE P Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 179)Suppliers
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BOC Sciences 16314854226; +16314854226 United States 19743 58 Inquiry
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Zhejiang J&C Biological Technology Co.,Limited +1-2135480471 +1-2135480471 China 10522 58 Inquiry

SUBSTANCE P Spectrum

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 SUBSTANCE P, F & D VERSION OF S6883*ACET ATE (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 SUBSTANCE P (HUMAN, BOVINE, RAT, MOUSE) SUBSTANCE P BOVINE SUBSTANCE P, [D-ARG1, D-PRO2, D-TRP7,9, LEU11] SUBSTANCE P (TYR8) SUBSTANCE P SUBSTANCE P AMIDE RPKPQFFGLM RPKPQQFFGLM-NH2 substance P (SP) 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-Gln-L-Gln-L-Phe-L-Phe-Gly-L-Leu-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 Neurokinin P P substance Sub Aids114081 Aids-114081 (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 H-Arg-Pro-Lys-Pro-Gln-Gln-Phe-Phe-Gly-Leu-Met-NH2 acetate salt Substance P TFA salt Substance P Acetate Substance P,Neurokinin P,Arg-Pro-Lys-Pro-Gln-Gln-Phe-Phe-Gly-Leu-Met-NH2,RPKPQQFFGLM-NH2?, >98% TYR8 SUBSTANCE P USP/EP/BP Substance P,Neurokinin P,Arg-Pro-Lys-Pro-Gln-Gln-Phe-Phe-Gly-Leu-Met-NH2,RPKPQQFFGLM-NH2 Substance P (9CI, ACI) NK receptor,Neurokinin Receptor,Endogenous Metabolite,Substance P,inhibit,Tachykinin receptor,Inhibitor 33507-63-0free/12769-48-1 P substance amide, Neurokinin P Amide sh-Oligopeptide-73 33507-63-0 C63H98N18O13S C63H98N18O13S1 Tachykinins Peptides Biochemicals and Reagents BioChemical Agonist Amino Acids and Peptides Peptide Tachykinin receptor TPI Peptide Receptors