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96382-72-8

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96382-72-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96382-72-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,3,8 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 96382-72:
(7*9)+(6*6)+(5*3)+(4*8)+(3*2)+(2*7)+(1*2)=168
168 % 10 = 8
So 96382-72-8 is a valid CAS Registry Number.
InChI:InChI=1/C27H34N6O6/c28-19(13-17-8-10-18(34)11-9-17)25(37)31-20-7-4-12-30-23(35)15-21(24(29)36)32-27(39)22(33-26(20)38)14-16-5-2-1-3-6-16/h1-3,5-6,8-11,19-22,34H,4,7,12-15,28H2,(H2,29,36)(H,30,35)(H,31,37)(H,32,39)(H,33,38)/t19-,20+,21-,22-/m0/s1

96382-72-8SDS

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 H-Tyr-D-Orn[*]-Phe-Asp[*]-NH2

1.2 Other means of identification

Product number -
Other names (2S,5S,12R)-12-[(S)-2-Amino-3-(4-hydroxy-phenyl)-propionylamino]-2-benzyl-3,7,13-trioxo-1,4,8-triaza-cyclotridecane-5-carboxylic acid amide

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:96382-72-8 SDS

96382-72-8Downstream Products

96382-72-8Relevant articles and documents

Conformationally Restricted Deltorphin Analogues

Schiller, Peter W.,Weltrowska, Grazyna,Nguyen, Thi M.-D.,Wilkes, Brian C.,Chung, Nga N.,Lemieux, Carole

, p. 3956 - 3961 (2007/10/02)

Conformationally restricted deltorphin analogues were synthesized either through incorporation of cyclic phenylalanine analogues in position 2 or 3 of the peptide sequence or through various side chain-to-side chain cyclizations.Compounds were tested in μ-, δ-, and κ-receptor selective binding assays and in the guinea pig ileum (GPI) and mouse vas deferens (MVD) bioassays.Replacement of Phe3 in 2>deltorphin I with 2-aminoindan-2-carboxylic acid (Aic) or L- or D-2-aminotetralin-2-carboxylic acid (Atc) resulted in agonist compounds which retained the high δ receptor selectivity of the parent peptide.Substitution of a tetrahydroisoquinoline-3-carboxylic acid (Tic) residue in the 2-position of 2>deltorphin I and 4,Nle6>deltorphin produced a partial δ agonist, H-Tyr-Tic-Phe-Asp-Val-Val-Gly-NH2, and a pure δ antagonist, H-Tyr-Tic-Phe-Phe-Leu-Nle-Asp-NH2, respectively.The later antagonist displayed high δ selectivity (Kiμ/Kiδ=502) and was a potent antagonist against selective δ agonists in the MVD assay (Ke ca. 10 nM).Various 2>-deltorphin I analogues cyclized between the side chains of Orn (or Lys) and Asp (or Glu) residues substituted in positions 2 and 4, 4 and 7, and 2 and 7 were essentially nonselective.Comparison with corresponding N-terminal tetrapeptide analogues revealed that the C-terminal tripeptide segment in the deltorphin heptapeptides made a crucial contribution to δ affinity and δ selectivity in the case of the agonist peptides but not in the case of the antagonist.

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