Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C28H37N5O7 |
| Molecular Weight | 555.6227 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@@H](N)CC2=CC=C(O)C=C2)C(O)=O
InChI
InChIKey=URLZCHNOLZSCCA-VABKMULXSA-N
InChI=1S/C28H37N5O7/c1-17(2)12-23(28(39)40)33-27(38)22(14-18-6-4-3-5-7-18)32-25(36)16-30-24(35)15-31-26(37)21(29)13-19-8-10-20(34)11-9-19/h3-11,17,21-23,34H,12-16,29H2,1-2H3,(H,30,35)(H,31,37)(H,32,36)(H,33,38)(H,39,40)/t21-,22-,23-/m0/s1
| Molecular Formula | C28H37N5O7 |
| Molecular Weight | 555.6227 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| A selective fluorescence reaction for peptides and chromatographic analysis. | 2008-03 |
|
| Translating DNA into synthetic molecules. | 2004-07 |
|
| DNA display III. Solid-phase organic synthesis on unprotected DNA. | 2004-07 |
|
| 2',6'-dimethylphenylalanine (Dmp) can mimic the N-terminal Tyr in opioid peptides. | 2004-02 |
|
| Characterization of human nasal primary culture systems to investigate peptide metabolism. | 2002-05-15 |
|
| Identification of dipeptidyl peptidase III in human neutrophils. | 2000-07-05 |
|
| Standard binding and functional assays related to medications development division testing for potential cocaine and opiate narcotic treatment medications. | 1998-03 |
|
| Pharmacological characterization of the cloned kappa-, delta-, and mu-opioid receptors. | 1994-02 |
|
| Cloning and pharmacological characterization of a rat kappa opioid receptor. | 1993-11-01 |
|
| Inhibition of vagal transmission by cardiac sympathetic nerve stimulation in the dog: possible involvement of opioid receptor. | 1989-09 |
|
| Seizures induced by carbachol, morphine, and leucine-enkephalin: a comparison. | 1983-04 |
|
| Anticonvulsants specific for petit mal antagonize epileptogenic effect of leucine enkephalin. | 1980-11-28 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:11:50 GMT 2025
by
admin
on
Mon Mar 31 18:11:50 GMT 2025
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| Record UNII |
RI01R707R6
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| Record Status |
Validated (UNII)
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| Record Version |
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| Code System | Code | Type | Description | ||
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461776
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58822-25-6
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350588
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LEU-ENKEPHALIN
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261-457-1
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89656
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RI01R707R6
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DTXSID00905127
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admin on Mon Mar 31 18:11:50 GMT 2025 , Edited by admin on Mon Mar 31 18:11:50 GMT 2025
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PRIMARY |