Ac-Pro-OH

CAS# 68-95-1

Ac-Pro-OH

Catalog No. BCC3017----Order now to get a substantial discount!

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Chemical structure

Ac-Pro-OH

3D structure

Chemical Properties of Ac-Pro-OH

Cas No. 68-95-1 SDF Download SDF
PubChem ID 322640 Appearance Powder
Formula C7H11NO3 M.Wt 157.2
Type of Compound N/A Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 1-acetylpyrrolidine-2-carboxylic acid
SMILES CC(=O)N1CCCC1C(=O)O
Standard InChIKey GNMSLDIYJOSUSW-UHFFFAOYSA-N
Standard InChI InChI=1S/C7H11NO3/c1-5(9)8-4-2-3-6(8)7(10)11/h6H,2-4H2,1H3,(H,10,11)
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months.
Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it.
About Packaging 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial.
2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial.
3. Try to avoid loss or contamination during the experiment.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request.

Ac-Pro-OH Dilution Calculator

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Ac-Pro-OH Molarity Calculator

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Preparing Stock Solutions of Ac-Pro-OH

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 6.3613 mL 31.8066 mL 63.6132 mL 127.2265 mL 159.0331 mL
5 mM 1.2723 mL 6.3613 mL 12.7226 mL 25.4453 mL 31.8066 mL
10 mM 0.6361 mL 3.1807 mL 6.3613 mL 12.7226 mL 15.9033 mL
50 mM 0.1272 mL 0.6361 mL 1.2723 mL 2.5445 mL 3.1807 mL
100 mM 0.0636 mL 0.3181 mL 0.6361 mL 1.2723 mL 1.5903 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

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Ac-Pro-OH

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References on Ac-Pro-OH

NMR conformational analysis of cis and trans proline isomers in the neutrophil chemoattractant, N-acetyl-proline-glycine-proline.[Pubmed:11246204]

Biopolymers. 2001 May;58(6):548-61.

Alkaline hydrolysis of corneal proteins in the alkali-injured eye releases N-acetyl-proline-glycine-proline (Ac-Pro-Gly-Pro-OH) among other peptides. It has been shown that this tripeptide is a neutrophil chemoattractant. Existing data suggest that the release of this peptide is the catalytic event for early neutrophil invasion of the cornea leading to corneal ulcers. In order to design inhibitors of this tripeptide chemoattractant that would block neutrophil invasion and diminish corneal ulcers, we studied the solution properties of this tripeptide by NMR spectroscopy and compared this peptide to Ac-Pro-Gly-OH (a weaker chemoattractant), and to Ac-Pro-OH (inactive). The NMR data were consistent with Ac-Pro-Gly-Pro-OH existing in solution as a mixture of four isomers with different cis and trans conformations about the two X-proline amide bonds. The isomer with two trans conformations (trans-trans) was the most dominant (41%) in aqueous solution. This was followed by the isomers with mixed cis and trans conformations (trans-cis, 26% and cis-trans, 20%). The isomer with two cis conformations (cis-cis) was the least favored (13%). The populations of these isomers were investigated in DMSO and they were similar to those reported in aqueous solutions except that the ordering of the trans-cis and cis-trans isomers were reversed. NMR NH temperature coefficients and nuclear Overhauser effect (NOE) measurements as well as CD spectroscopy were used to demonstrate that the four isomers exist primarily in an extended conformation with little hydrogen bonding. The available (NOE) information was used with molecular dynamics calculations to construct a dominant solution conformation for each isomer of the tripeptide. This information will serve as a model for the design of peptide and nonpeptide inhibitors of the chemoattractant.

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