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Cosmetics Grade 1-(2-hydroxy-2-phenylethyl)pyrrolidine-2,5-dione 68239-22-5 For Sale with Good Price
- Molecular Formula: C12H13NO3
- Molecular Weight: 219.24
- Vapor Pressure: 1.03E-08mmHg at 25°C
- Boiling Point: 445.4°Cat760mmHg
- Flash Point: 223.2°C
- PSA: 57.61000
- Density: 1.294g/cm3
- LogP: 0.80690
1-(2-hydroxy-2-phenylethyl)pyrrolidine-2,5-dione(Cas 68239-22-5) Usage
|
Synonym |
(S)-HPHPD |
|
Classification |
Pyrrolidine-2,5-dione derivative |
|
Parent compound |
Amino acid proline |
|
Potential pharmaceutical application |
Inhibitor of prolyl hydroxylase enzyme |
|
Enzyme target |
Prolyl hydroxylase |
|
Enzyme function |
Regulation of hypoxia-inducible factor (HIF) |
|
HIF role |
Oxygen homeostasis regulation |
|
Associated diseases |
Cancer, ischemic heart disease |
|
Therapeutic potential |
Treatment of conditions related to HIF pathway modulation |
|
Current status |
Further research needed to understand potential uses and mechanisms of action |
|
General Description |
1-(2-hydroxy-2-phenylethyl)pyrrolidine-2,5-dione, also known as (S)-HPHPD, is a chemical compound with a molecular formula C12H13NO3. It is a derivative of the amino acid proline and is classified as a pyrrolidine-2,5-dione. 1-(2-hydroxy-2-phenylethyl)pyrrolidine-2,5-dione has been studied for its potential as a pharmaceutical agent, particularly for its use as an inhibitor of the enzyme prolyl hydroxylase. Prolyl hydroxylase is involved in the regulation of hypoxia-inducible factor (HIF), which plays a role in oxygen homeostasis and is associated with diseases such as cancer and ischemic heart disease. (S)-HPHPD may have therapeutic applications in the treatment of these conditions by modulating the HIF pathway. Further research is needed to fully understand the potential uses and mechanisms of action of this compound. |
InChI:InChI=1/C12H13NO3/c14-10(9-4-2-1-3-5-9)8-13-11(15)6-7-12(13)16/h1-5,10,14H,6-8H2
68239-22-5 Relevant articles
Preparation and Reactivity of Highly Functionalized Organometallics at the α Position of Oxygen or Nitrogen
Knochel, Paul,Chou, Tso-Sheng,Jubert, Carole,Rajagopal, Duddu
, p. 588 - 599 (2007/10/02)
α-Halogenoalkyl carboxylates (FG-R1CH(X)...
Base-catalyzed carbon-carbon bond formation reactions of ω-hydroxylactams
Speckamp, W. N.,Boer, J. J. J. de
, p. 410 - 414 (2007/10/02)
Active methylene compounds such as methy...
68239-22-5 Process route
-
-
54553-14-9
succinic acid N-(chloromethyl)imide
-
-
100-52-7
benzaldehyde
-
-
68239-22-5
N-(2-hydroxy-2-phenylethyl)-2,5-pyrrolidinedione
| Conditions | Yield |
|---|---|
|
With
chromium dichloride; lithium iodide;
In
tetrahydrofuran;
at 50 ℃;
for 6h;
|
84%
|
-
-
123-56-8,89963-74-6
Succinimide
-
-
96-09-3
styrene oxide
-
-
68239-22-5
N-(2-hydroxy-2-phenylethyl)-2,5-pyrrolidinedione
| Conditions | Yield |
|---|---|
|
With
sodium hydroxide; water;
at 150 - 160 ℃;
|
|
|
With
pyridine; butan-1-ol;
|
|
|
With
sodium;
In
ethanol;
for 18h;
Heating;
|
13.0 g
|
|
With
N,N-dimethyl-formamide;
|
68239-22-5 Upstream products
-
123-56-8
Succinimide
-
96-09-3
styrene oxide
-
54553-14-9
succinic acid N-(chloromethyl)imide
-
100-52-7
benzaldehyde
68239-22-5 Downstream products
-
106272-54-2
N -(β-acetoxy-phenethyl)-succinimide
-
99989-77-2
N -(4-nitro-β-nitryloxy-phenethyl)-succinimide
-
7568-93-6
2-Amino-1-phenylethanol
-
120542-02-1
N-[(E)-2-phenylvinyl]succinimide
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