Hippuryl-Phe-OH
Names
[ CAS No. ]:
744-59-2
[ Name ]:
Hippuryl-Phe-OH
[Synonym ]:
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
Biological Activity
[Description]:
[Related Catalog]:
[References]
Chemical & Physical Properties
[ Density]:
1.3±0.1 g/cm3
[ 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
Safety Information
[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
[ Safety Phrases ]:
S22-S24/25
[ RIDADR ]:
NONH for all modes of transport
[ HS Code ]:
2924299090
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2924299090
[ 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%
Articles
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...
Mast cell proteases.Meth. Enzymol. 80 , 588, (1981)
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 (...