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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

1-5-Adrenorphin (human)

CSCC[C@@H](C(=O)O)NC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)CNC(=O)[C@H](Cc1ccc(cc1)O)N Request for Quotation
Chemical Name: 1-5-Adrenorphin (human)
CAS Number: 58569-55-4
Product Number: AG00E8Q0(AGN-PC-0SQ3WS)
Synonyms:
MDL No:
Molecular Formula: C27H35N5O7S
Molecular Weight: 573.6611

Identification/Properties

Computed Properties
Molecular Weight:
573.665g/mol
XLogP3:
-2.1
Hydrogen Bond Donor Count:
7
Hydrogen Bond Acceptor Count:
9
Rotatable Bond Count:
16
Exact Mass:
573.226g/mol
Monoisotopic Mass:
573.226g/mol
Topological Polar Surface Area:
225A^2
Heavy Atom Count:
40
Formal Charge:
0
Complexity:
847
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
3
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


H-Tyr-Gly-Gly-Phe-Met-OH is a peptide compound commonly used in chemical synthesis for its unique properties and versatile applications. This peptide, composed of the amino acids tyrosine, glycine, phenylalanine, and methionine, offers numerous benefits in various synthetic processes. Its precise structure and specific amino acid sequence make it an ideal choice for peptide synthesis and drug development. In chemical reactions, H-Tyr-Gly-Gly-Phe-Met-OH can serve as a building block to create more complex peptides or molecules with enhanced biological activity. Additionally, this peptide can be utilized as a research tool to study protein-protein interactions, enzyme kinetics, and drug-receptor interactions. Its stable structure and reactivity make it a valuable component in the field of medicinal chemistry and pharmaceutical research.