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CAS

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125741-45-9

substance P (6-11), N(1,6)(beta-glucopyranosyl)Glu(5)-Pro(9)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 125741-45-9 Structure

  • Basic information

    1. Product Name: substance P (6-11), N(1,6)(beta-glucopyranosyl)Glu(5)-Pro(9)-
    2. Synonyms: substance P (6-11), N(1,6)(beta-glucopyranosyl)Glu(5)-Pro(9)-
    3. CAS NO:125741-45-9
    4. Molecular Formula: C45H65N7O13S
    5. Molecular Weight: 944.1017
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 125741-45-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 1268.6°Cat760mmHg
    3. Flash Point: 721°C
    4. Appearance: /
    5. Density: 1.38g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.634
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 12.52±0.70(Predicted)
    11. CAS DataBase Reference: substance P (6-11), N(1,6)(beta-glucopyranosyl)Glu(5)-Pro(9)-(CAS DataBase Reference)
    12. NIST Chemistry Reference: substance P (6-11), N(1,6)(beta-glucopyranosyl)Glu(5)-Pro(9)-(125741-45-9)
    13. EPA Substance Registry System: substance P (6-11), N(1,6)(beta-glucopyranosyl)Glu(5)-Pro(9)-(125741-45-9)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 125741-45-9(Hazardous Substances Data)

125741-45-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 125741-45-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,7,4 and 1 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 125741-45:
(8*1)+(7*2)+(6*5)+(5*7)+(4*4)+(3*1)+(2*4)+(1*5)=119
119 % 10 = 9
So 125741-45-9 is a valid CAS Registry Number.
InChI:InChI=1/C45H65N7O13S/c1-25(2)21-31(50-40(60)29-15-10-19-47-29)41(61)48-30(18-20-66-3)43(63)52(45-38(58)37(57)36(56)34(24-53)65-45)44(64)33(23-27-13-8-5-9-14-27)51-42(62)32(22-26-11-6-4-7-12-26)49-39(59)28(46)16-17-35(54)55/h4-9,11-14,25,28-34,36-38,45,47,53,56-58H,10,15-24,46H2,1-3H3,(H,48,61)(H,49,59)(H,50,60)(H,51,62)(H,54,55)/t28-,29-,30-,31-,32-,33-,34+,36+,37-,38+,45+/m0/s1

125741-45-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name L-glutamyl (γ-β-D-glucopyranosyl)-L-phenylalanyl-L-phenylalanyl-L-prolyl-L-leucyl-L-methionine amide

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:125741-45-9 SDS

125741-45-9Downstream Products

125741-45-9Relevant articles and documents

A synthetic glycopeptide of substance P analogue (SP6-11) with enhanced NK-1 receptor specificity

Haro,Busquets,Torres,Valencia,Garcia-Anton,Reig

, p. 74 - 76 (2007/10/02)

A new glycopeptide analogue of substance P (6-11) (SP6-11), namely, N1,6 (β-D-glucopyranosyl) [Glu6, Pro9]SP6-11, has been synthesized and found to be water soluble. The in vitro biological activity of this glycopeptide was determined for spasmogenic activity in the guinea pig ileum and for potentiation of electrically evoked contractions in the rat vas deferens. Thus, activities of NK-1, NK-2, and NK-3 receptor types have been differentiated by two assays and, in the case of NK-1 and NK-3, receptors in guinea pig ileum (GPI) were assayed using specific pharmacological procedures. The ED50 values for the analogue and reference peptides substance P (SP), neurokinin A(NKA), and neurokinin B (NKB) were determined and potencies relative to SP were calculated. The analogue is three times more potent than the potent NK-1 agonist SP on NK-1 receptors. Moreover, this glycopeptide proved to be as selective for the NK-1 receptor as the specific agonist SPOMe (the methyl ester of substance P).

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