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Fmoc-D-Bip(4,4)-OH

Names

[ CAS No. ]:
205526-38-1

[ Name ]:
Fmoc-D-Bip(4,4)-OH

[Synonym ]:
(2R)-3-(4-Biphenylyl)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}propanoic acid
FMOC-D-BPH-OH
FMOC-L-BIP-OH
FMOC-BIP-OH
FMOC-D-BIP(4,4')-OH
FMOC-4-PHENYL-PHE-OH
(2S)-3-(Biphenyl-4-yl)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}propanoic acid (non-preferred name)
FMOC-L-PHE(4-PH)-OH
Fmoc-D-phe(4-ph)-OH
3-(4-Biphenylyl)-N-Fmoc-D-alanine
FMOC-BIP(4,4')-OH
FMOC-BPH-OH
(2R)-3-(Biphenyl-4-yl)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}propanoic acid (non-preferred name)
FMOC-L-PHE(4-PH)
(2S)-3-(4-Biphenylyl)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}propanoic acid
N-[(9H-fluoren-9-ylmethoxy)carbonyl]-D-4,4'-biphenylalanine
MFCD00191198
FMOC-D-BIP-OH
Fmoc-D-Bip(4,4)-OH

Biological Activity

[Description]:

Fmoc-D-Bip(4,4’)-OH is an alanine derivative[1].

[Related Catalog]:

Research Areas >> Others
Signaling Pathways >> Others >> Others

[In Vitro]

Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1].

[References]

[1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1074.

Chemical & Physical Properties

[ Density]:
1.3±0.1 g/cm3

[ Boiling Point ]:
700.7±60.0 °C at 760 mmHg

[ Molecular Formula ]:
C30H25NO4

[ Molecular Weight ]:
463.524

[ Flash Point ]:
377.6±32.9 °C

[ Exact Mass ]:
463.178345

[ PSA ]:
75.63000

[ LogP ]:
7.16

[ Vapour Pressure ]:
0.0±2.3 mmHg at 25°C

[ Index of Refraction ]:
1.641

[ Storage condition ]:
2-8°C

Safety Information

[ Hazard Codes ]:
Xi

Related Compounds