Basic information
- CAS
31325-39-0- Standard SMILES
N[C@@H](CCC(=O)O)C(=O)O.N[C@@H](Cc1ccc(O)cc1)C(=O)O- InChIKey
LZKJGAQEZMGEBN-YYTBSQRUSA-N- Molecular formula
- C14H20N2O7
- Average molar mass
- 328.32 g/mol
- Monoisotopic mass
- 328.12705098
Overview
synthetic polypeptide which has suppressive effect on delayed-type hypersensitivity
Names & identifiers
- Preferred name
- L-Glutamic acid-L-tyrosine copolymer
- IUPAC
- (2S)-2-amino-3-(4-hydroxyphenyl)propanoic acid;(2S)-2-aminopentanedioic acid
- English name
- L-glutamic acid-L-tyrosine copolymer
- Molecular formula
- C14H20N2O7
- Molecular weight
- 328.32
Names & synonyms
RefChem:92441031325-39-0DTXCID60107746DTXSID50185255SCHEMBL362131L-glutamic acid-L-tyrosine copolymer
Database identifiers
- CAS
31325-39-0- PubChem CID
- 65384
- DTXSID
DTXSID50185255
Properties
Computed structural properties
- Topological polar surface area
- 184 Ų
- Hydrogen bond donors
- 6
- Hydrogen bond acceptors
- 9
- Rotatable bonds
- 7
- Heavy atoms
- 23
- Formal charge
- 0
- Complexity
- 320
Chemistry & industry
Pharmacology
MeSH Pharmacological Classification
Agents that suppress immune function by one of several mechanisms of action. Classical cytotoxic immunosuppressants act by inhibiting DNA synthesis. Others may act through activation of T-CELLS or by inhibiting the activation of HELPER CELLS. While immunosuppression has been brought about in the past primarily to prevent rejection of transplanted organs, new applications involving mediation of the effects of INTERLEUKINS and other CYTOKINES are emerging.
Related reactions
0 records
No reaction records under the current filter.
Compound notes
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