Hippuryl-Phe-OH structure
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Common Name | Hippuryl-Phe-OH | ||
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CAS Number | 744-59-2 | Molecular Weight | 326.346 | |
Density | 1.3±0.1 g/cm3 | Boiling Point | 673.3±55.0 °C at 760 mmHg | |
Molecular Formula | C18H18N2O4 | Melting Point | 140-144ºC | |
MSDS | Chinese USA | Flash Point | 361.0±31.5 °C |
Use of Hippuryl-Phe-OHHippuryl-L-phenylalanine is a substrate of carboxypeptidase. Carboxypeptidase is a protease enzyme that related with obesity, epilepsy and neurodegeneration. Hippuryl-L-phenylalanine can be used for the determination of carboxypeptidase activity[1][2]. |
Name | n-benzoyl-gly-phe |
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Synonym | More Synonyms |
Description | Hippuryl-L-phenylalanine is a substrate of carboxypeptidase. Carboxypeptidase is a protease enzyme that related with obesity, epilepsy and neurodegeneration. Hippuryl-L-phenylalanine can be used for the determination of carboxypeptidase activity[1][2]. |
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Related Catalog | |
References |
Density | 1.3±0.1 g/cm3 |
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Boiling Point | 673.3±55.0 °C at 760 mmHg |
Melting Point | 140-144ºC |
Molecular Formula | C18H18N2O4 |
Molecular Weight | 326.346 |
Flash Point | 361.0±31.5 °C |
Exact Mass | 326.126648 |
PSA | 95.50000 |
LogP | 2.18 |
Vapour Pressure | 0.0±2.2 mmHg at 25°C |
Index of Refraction | 1.600 |
Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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Safety Phrases | S22-S24/25 |
RIDADR | NONH for all modes of transport |
HS Code | 2924299090 |
~75% Hippuryl-Phe-OH CAS#:744-59-2 |
Literature: Litvinenko, L. M.; Kosmynin, V. V.; Kaida, L. N.; Savelova, V. A.; Verbovaya, I. P. Journal of Organic Chemistry USSR (English Translation), 1986 , vol. 22, # 4 p. 784 - 785 Zhurnal Organicheskoi Khimii, 1986 , vol. 22, # 4 p. 877 - 878 |
~69% Hippuryl-Phe-OH CAS#:744-59-2 |
Literature: Chung-hsi, Li; Yuen-hwa, Yieh; Yao, Lin; Yong-jun, Lu; Ai-hsueh, Chi; Chi-yi, Hsing Tetrahedron Letters, 1981 , vol. 22, # 36 p. 3467 - 3470 |
~% Hippuryl-Phe-OH CAS#:744-59-2 |
Literature: Tetrahedron Letters, , vol. 22, # 36 p. 3467 - 3470 |
~% Hippuryl-Phe-OH CAS#:744-59-2 |
Literature: Tetrahedron Letters, , vol. 22, # 36 p. 3467 - 3470 |
~% Hippuryl-Phe-OH CAS#:744-59-2 |
Literature: Tetrahedron Letters, , vol. 22, # 36 p. 3467 - 3470 |
~% Hippuryl-Phe-OH CAS#:744-59-2 |
Literature: J. Gen. Chem. USSR (Engl. Transl.), , vol. 39, # 1 p. 92 - 96,81 - 83 |
~% Hippuryl-Phe-OH CAS#:744-59-2 |
Literature: J. Gen. Chem. USSR (Engl. Transl.), , vol. 39, # 1 p. 92 - 96,81 - 83 |
~% Hippuryl-Phe-OH CAS#:744-59-2 |
Literature: J. Gen. Chem. USSR (Engl. Transl.), , vol. 39, # 1 p. 92 - 96,81 - 83 |
Precursor 9 | |
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DownStream 5 | |
HS Code | 2924299090 |
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Summary | 2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% |
Structural and functional characterization of ochratoxinase, a novel mycotoxin-degrading enzyme.
Biochem. J. 462(3) , 441-52, (2014) Ochratoxin, with ochratoxin A as the dominant form, is one of the five major mycotoxins most harmful to humans and animals. It is produced by Aspergillus and Penicillium species and occurs in a wide r... |
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Mast cell proteases.
Meth. Enzymol. 80 , 588, (1981)
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Mechanisms for activation and inhibition of carboxypeptidase A catalyzed hydrolyses of peptides and esters.
Can. J. Biochem. 56 , 329, (1978) 3,3-Diphenylpropanoate (DPP) activates the carboxypeptidase A catalyzed hydrolysis of benzoylglycyl-L-phenylalanine (BzGly-L-Phe) (Ka = 2.1 x 10 (-3) M) and inhibits ester hydrolysis uncompetitively (... |
HIPPURYL-PHE-OH |
BENZOYL-GLY-L-PHE |
MFCD00037265 |
HIPPURYL-L-PHE |
HIPP-L-PHE |
Einecs 212-016-7 |
hippurylphenylalanine |
L-Phenylalanine, N-benzoylglycyl- |
hippuryl-L-phenylalanine |
BENZOYL-GLY-PHE |
HIPPURYL-PHE |
BZ-GLY-PHE-OH |
N-Benzoylglycyl-L-phenylalanine |