CAS 2578-57-6: L-Prolylglycine
Formula:C7H12N2O3
InChI:InChI=1S/C7H12N2O3/c10-6(11)4-9-7(12)5-2-1-3-8-5/h5,8H,1-4H2,(H,9,12)(H,10,11)/t5-/m0/s1
InChI key:InChIKey=RNKSNIBMTUYWSH-YFKPBYRVSA-N
SMILES:C(NCC(O)=O)(=O)[C@@H]1CCCN1
Synonyms:- 103: PN: EP2161028 PAGE: 10 claimed protein
- 1: PN: KR20100018632 PAGE: 3 claimed protein
- 2-[(2S)-Pyrrolidin-2-ylformamido]acetic acid
- 2-[[(2S)-Pyrrolidin-1-ium-2-carbonyl]amino]acetate
- 2: PN: WO2010117786 PAGE: 166 claimed protein
- 42: PN: US20130123467 SEQID: 47 claimed protein
- 45: PN: WO03052099 PAGE: 84 claimed protein
- 84: PN: WO2017078631 PAGE: 50 claimed protein
- <span class="text-smallcaps">L</span>-Prolylglycine
- Glycine, <span class="text-smallcaps">L</span>-prolyl-
- Glycine, N-<span class="text-smallcaps">L</span>-prolyl-
- See more synonyms
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Found 4 products.
H-Pro-Gly-OH
CAS:Substrate for prolinase (prolyl dipeptidase).Formula:C7H12N2O3Purity:> 99%Color and Shape:White PowderMolecular weight:172.18Pro-Gly-OH
CAS:Pro-Gly-OH is a cyclic peptide that has been shown to have antimicrobial activity. Pro-Gly-OH has been shown to be an intramolecular hydrogen acceptor, which leads to the formation of a carbonyl group. This compound also has site specific interactions with the cell membrane and is taken up by cells. It is active at acidic pHs and can be activated by growth factors. The conformational properties of Pro-Gly-OH are due to hydrogen bonding interactions and amide bond formation.Formula:C7H12N2O3Purity:Min. 95%Color and Shape:PowderMolecular weight:172.18 g/molPro-Gly-OH
CAS:Purity:95.0%Color and Shape:Liquid, No data available.Molecular weight:172.1840057373047
