202739-37-5
Chemical Structure
Ac-Ala-Ala-Ser(PO3H2)-Pro-Arg-NH-Np
- CAS No.: 202739-37-5
- Formula:C28H43N10O12P
- Molecular Weight:742.67
IUPAC Name: (S)-2-((S)-2-((S)-2-acetamidopropanamido)propanamido)-3-((S)-2-(((S)-5-guanidino-1-((4-nitrophenyl)amino)-1-oxopentan-2-yl)carbamoyl)pyrrolidin-1-yl)-3-oxopropyl dihydrogen phosphate
InChIKey: NBXGKBASYKEBOZ-OPXVNJCFSA-N
SMILES: O=P(O)(OC[C@H](NC([C@@H](NC([C@@H](NC(C)=O)C)=O)C)=O)C(N1[C@H](C(N[C@@H](CCCNC(N)=N)C(NC2=CC=C([N+]([O-])=O)C=C2)=O)=O)CCC1)=O)O
Biological Activity: Ac-Ala-Ala-Ser (PO3H2)-Pro-Arg-NH-Np is a PIN1 substrate that undergoes cis-trans isomerization of the peptidyl-prolyl bond under the catalysis of human PIN1 and yeast Ess1. Ac-Ala-Ala-Ser (PO3H2)-Pro-Arg-NH-Np can be used in breast cancer-related research[1][2].
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Ac-Ala-Ala-Ser(PO3H2)-Pro-Arg-NH-Np | Ac-Ala-Ala-Ser (PO3H2)-Pro-Arg-NH-Np is a PIN1 substrate that undergoes cis-trans isomerization of the peptidyl-prolyl bond under the catalysis of human PIN1 and yeast Ess1. Ac-Ala-Ala-Ser (PO3H2)-Pro-Arg-NH-Np can be used in breast cancer-related research. | |||||||||||||||||||||
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Keywords
