1. Home
  2. H-Gly-Gly-His-OH

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

H-Gly-Gly-His-OH

NCC(=O)NCC(=O)N[C@H](C(=O)O)Cc1cnc[nH]1 Request for Quotation
Chemical Name: H-Gly-Gly-His-OH
CAS Number: 93404-95-6
Product Number: AG00GV4A(AGN-PC-0WAIMD)
Synonyms:
MDL No:
Molecular Formula: C10H15N5O4
Molecular Weight: 269.2572

Identification/Properties

Computed Properties
Molecular Weight:
269.261g/mol
XLogP3:
-4.5
Hydrogen Bond Donor Count:
5
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
7
Exact Mass:
269.112g/mol
Monoisotopic Mass:
269.112g/mol
Topological Polar Surface Area:
150A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
349
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


H-Gly-Gly-His-OH, also known as Glycyl-Glycyl-Histidine, is a peptide compound commonly used in chemical synthesis applications. This specific peptide sequence is valuable in biochemistry and pharmaceutical research for its ability to mimic a portion of natural proteins, making it a versatile building block for creating novel peptide analogs with desired properties. In chemical synthesis, H-Gly-Gly-His-OH serves as a key component in the assembly of complex peptide structures, enabling researchers to explore the structure-activity relationships of peptides and design new molecules for various biological and medicinal applications. Its strategic placement can influence the overall conformation and function of the synthesized peptides, making it a valuable tool for studying protein-protein interactions, enzyme mechanisms, and drug discovery.