Prezatide monoacetateProduct ingredient for Prezatide
- Name
- Prezatide monoacetate
- Drug Entry
- Prezatide
Prezatide is a tripeptide consisting of glycine, histidine, and lysine which readily forms a complex with copper ions 6. Prezatide is used in cosmetic products for the skin and hair. It is known to aid wound healing and its potential applications in chronic obstructive pulmonary disease and metastatic colon cancer are currently being investigated.
- Accession Number
- DBSALT002421
- Structure
Structure for Prezatide monoacetate (DBSALT002421)
- Synonyms
- GHK acetate / PC-1020 monoacetate
- UNII
- 8AA809EUS9
- CAS Number
- 72957-37-0
- Weight
- Average: 400.436
Monoisotopic: 400.207032646 - Chemical Formula
- C16H28N6O6
- InChI Key
- MGNUTAFMLGJBGV-ACMTZBLWSA-N
- InChI
- InChI=1S/C14H24N6O4.C2H4O2/c15-4-2-1-3-10(14(23)24)20-13(22)11(19-12(21)6-16)5-9-7-17-8-18-9;1-2(3)4/h7-8,10-11H,1-6,15-16H2,(H,17,18)(H,19,21)(H,20,22)(H,23,24);1H3,(H,3,4)/t10-,11-;/m0./s1
- IUPAC Name
- (2S)-6-amino-2-[(2S)-2-(2-aminoacetamido)-3-(1H-imidazol-4-yl)propanamido]hexanoic acid; acetic acid
- SMILES
- CC(O)=O.NCCCC[C@H](NC(=O)[C@H](CC1=CNC=N1)NC(=O)CN)C(O)=O
- External Links
- ChemSpider
- 20041111
- Predicted Properties
Property Value Source Water Solubility 3.14 mg/mL ALOGPS logP -3 ALOGPS logP -5.1 Chemaxon logS -2 ALOGPS pKa (Strongest Acidic) 3.46 Chemaxon pKa (Strongest Basic) 10.2 Chemaxon Physiological Charge 1 Chemaxon Hydrogen Acceptor Count 7 Chemaxon Hydrogen Donor Count 6 Chemaxon Polar Surface Area 176.22 Å2 Chemaxon Rotatable Bond Count 11 Chemaxon Refractivity 84.91 m3·mol-1 Chemaxon Polarizability 34.57 Å3 Chemaxon Number of Rings 1 Chemaxon Bioavailability 0 Chemaxon Rule of Five No Chemaxon Ghose Filter No Chemaxon Veber's Rule No Chemaxon MDDR-like Rule No Chemaxon