Glycyl-L-Histidyl-L-Lysine CAS#: 49557-75-7; ChemWhat Code: 91015
Identification
Patent Information | ||
Patent ID | Title | Publication Date |
US2007/4633 | Use of peptidic conjugates for preparing compositions for alopecia preventive and curative treatment | 2007 |
US4810693 | Method for inducing biological coverings in wounds | 1989 |
Physical Data
Appearance | White powder |
Solubility | No data available |
Boiling Point | 831.0±65.0 °C(Predicted) |
Refractive index | No data available |
Sensitivity | No data available |
Description (Association (MCS)) | Solvent (Association (MCS)) | Temperature (Association (MCS)), °C | Partner (Association (MCS)) |
Stability constant of the complex with … | various solvent(s) | 25 | [5,10,15,20-tetrakis(4-carboxy-3,5-bis(carboxymethoxy)phenyl)porphyrinato]zinc(II) potassium salt |
Stability constant of the complex with … | various solvent(s) | 25 | [5,10,15,20-tetrakis(4-carboxy-3,5-bis(10-carboxydecyloxy)phenyl)porphyrinato]zinc(II) potassium salt |
Stability constant of the complex with … | various solvent(s) | 25 | 5,10,15,20-tetrakis(4-carboxyphenyl)porphirinatozinc acetate |
Stability constant of the complex with … | various solvent(s) | 25 | [5,10,15,20-tetrakis(4-carboxy-3,5-bis(carboxybutoxy)phenyl)porphyrinato]zinc(II) potassium salt |
Spectra
Description (NMR Spectroscopy) | Nucleus (NMR Spectroscopy) | Solvents (NMR Spectroscopy) | Temperature (NMR Spectroscopy), °C | Frequency (NMR Spectroscopy), MHz |
Chemical shifts, Spectrum | 13C | water-d2 | 24.84 | 125.8 |
Chemical shifts, Spectrum | 1H | water-d2 | 24.84 | 500 |
Chemical shifts | 1H | 300 |
Description (Mass Spectrometry) | Comment (Mass Spectrometry) |
MALDI (Matrix assisted laser desorption ionization), time-of-flight mass spectra (TOFMS), spectrum | |
Molecular peak |
Description (UV/VIS Spectroscopy) | Solvent (UV/VIS Spectroscopy) |
Spectrum | water |
Description (ESR Spectroscopy) | Solvents (ESR Spectroscopy) | Temperature (ESR Spectroscopy), °C |
Spectrum | water | 25 |
Route of Synthesis (ROS)
Conditions | Yield |
With sodium methylate In methanol; water at 20℃; for 2h; Experimental Procedure 1 Example 1 Preparation of the peptide metalocomplex Cu-GHK 1.5 g of GHK was suspended at ambient temperature in 50 ml of 100percent methanol, while stirred continuously 0.25 g of cupric acetate (CuOAc) was added in the form of 5 ml of aqueous solution and 5 ml of MeONa (1M). The mixture was stirred at ambient temperature at the speed of 130 rpm for 120 minutes. The peptide metalocomplex was then extracted and dried. |
Safety and Hazards
GHS Hazard Statements | Not Classified |
Precautionary Statement Codes |
Other Data
Transportation | Not dangerous goods |
Under the room temperature and away from light | |
HS Code | No data available |
Storage | Under the room temperature and away from light |
Shelf Life | 1 year |
Market Price | USD |
Druglikeness | |
Lipinski rules component | |
Molecular Weight | 340.382 |
logP | -4.37 |
HBA | 10 |
HBD | 6 |
Matching Lipinski Rules | 3 |
Veber rules component | |
Polar Surface Area (PSA) | 176.22 |
Rotatable Bond (RotB) | 13 |
Matching Veber Rules | 0 |
Use Pattern |
Glycyl-L-Histidyl-L-Lysine CAS#: 49557-75-7 used in cosmetics. |
Glycyl-L-Histidyl-L-Lysine CAS#: 49557-75-7 can protect collagen from damage by activated carbon groups. |
Glycyl-L-Histidyl-L-Lysine CAS#: 49557-75-7 can promote the growth of type III collagen. |
Glycyl-L-Histidyl-L-Lysine CAS#: 49557-75-7 can anti-glycation |
Glycyl-L-Histidyl-L-Lysine CAS#: 49557-75-7 is can anti-oxidation. |
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Apnoke Scientific Ltd | http://www.apnoke.com/ |
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