H-Pro-Val-OH

Modify Date: 2025-09-21 12:15:44

H-Pro-Val-OH structure	Common Name	H-Pro-Val-OH
	CAS Number	52899-09-9	Molecular Weight	214.26
	Density	1.15g/cm3	Boiling Point	451.1ºC at 760mmHg
	Molecular Formula	C₁₀H₁₈N₂O₃	Melting Point	N/A
	MSDS	USA	Flash Point	226.6ºC

Use of H-Pro-Val-OH

H-Pro-Val-OH is a deprotonation dipeptide containing proline, which can catalyze the Michael addition reaction of acetone to trans-β-nitrostyrene. H-Pro Val OH can also serve as a substrate for fibroblast enzymes and prolinase, and has potential applications in biochemical analysis[1][2][3][4].

Name	h-pro-val-oh
Synonym	More Synonyms

Description	H-Pro-Val-OH is a deprotonation dipeptide containing proline, which can catalyze the Michael addition reaction of acetone to trans-β-nitrostyrene. H-Pro Val OH can also serve as a substrate for fibroblast enzymes and prolinase, and has potential applications in biochemical analysis[1][2][3][4].
Related Catalog	Research Areas >> Others Signaling Pathways >> Others >> Others
References	[1]. Harrison AG, et al. Fragmentation reactions of deprotonated peptides containing proline. The proline effect. J Mass Spectrom. 2005 Sep;40(9):1173-86. [2]. Davie EA, et al. Asymmetric catalysis mediated by synthetic peptides. Chem Rev. 2007 Dec;107(12):5759-812. [3]. Uramatsu M, et al. Different effects of sulfur amino acids on prolidase and prolinase activity in normal and prolidase-deficient human erythrocytes. Clin Chim Acta. 2007 Jan;375(1-2):129-35. [4]. Myara I, et al. Determination of prolinase activity in plasma. Application to liver disease and its relation with prolidase activity. Clin Biochem. 1985 Aug;18(4):220-3.

Description

Related Catalog

Research Areas >> Others

Signaling Pathways >> Others >> Others

References

[1]. Harrison AG, et al. Fragmentation reactions of deprotonated peptides containing proline. The proline effect. J Mass Spectrom. 2005 Sep;40(9):1173-86.

[2]. Davie EA, et al. Asymmetric catalysis mediated by synthetic peptides. Chem Rev. 2007 Dec;107(12):5759-812.

[3]. Uramatsu M, et al. Different effects of sulfur amino acids on prolidase and prolinase activity in normal and prolidase-deficient human erythrocytes. Clin Chim Acta. 2007 Jan;375(1-2):129-35.

[4]. Myara I, et al. Determination of prolinase activity in plasma. Application to liver disease and its relation with prolidase activity. Clin Biochem. 1985 Aug;18(4):220-3.

Density	1.15g/cm3
Boiling Point	451.1ºC at 760mmHg
Molecular Formula	C₁₀H₁₈N₂O₃
Molecular Weight	214.26
Flash Point	226.6ºC
Exact Mass	214.13200
PSA	78.43000
LogP	0.68350
Index of Refraction	1.449
InChIKey	AWJGUZSYVIVZGP-UHFFFAOYSA-N
SMILES	CC(C)C(NC(=O)C1CCCN1)C(=O)O

HS Code	2933990090

HS Code	2933990090
Summary	2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

L-Pro-L-Val

PRO-VAL

PROLINE-VALINE

L-prolyl-L-valine

L-Propyl-L-valine

(S)-prolyl-(S)-valine

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