Fmoc-D-Phe-OH

Names

[ Name ]:
Fmoc-D-Phe-OH

[Synonym ]:
Fmoc-(D)-Phe-NH2
(R)-Fmoc-phenylalanine
fmoc-d-phe
N-Fmoc-D-phenylalanine
D-Phenylalanine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-
Fmoc-D-Phe-OH
Fmoc-D-phenylalanine-OH
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-D-phenylalanine
MFCD00062955
Fmoc-D-phenylalanine
Fmoc-phenylalanine

Biological Activity

[Description]:

Fmoc-D-Phe-OH is a phenylalanine 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):1793-815.

Chemical & Physical Properties

[ Density]:
1.3±0.1 g/cm3

[ Boiling Point ]:
620.1±50.0 °C at 760 mmHg

[ Melting Point ]:
181-185ºC

[ Molecular Formula ]:
C₂₄H₂₁NO₄

[ Molecular Weight ]:
387.428

[ Flash Point ]:
328.8±30.1 °C

[ Exact Mass ]:
387.147064

[ PSA ]:
75.63000

[ LogP ]:
5.41

[ Vapour Pressure ]:
0.0±1.9 mmHg at 25°C

[ Index of Refraction ]:
1.633

[ Storage condition ]:
2-8°C

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xi

[ Safety Phrases ]:
S22-S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2924299090

Synthetic Route

Click to get detail 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

1,4-disubstituted-[1,2,3]triazolyl-containing analogues of MT-II: design, synthesis, conformational analysis, and biological activity.

J. Med. Chem. 57(22) , 9424-34, (2014)

Side chain-to-side chain cyclizations represent a strategy to select a family of bioactive conformations by reducing the entropy and enhancing the stabilization of functional ligand-induced receptor c...

Solid-phase synthesis of C-terminal azapeptides.

J. Pept. Sci. 21 , 387-91, (2015)

The solid-phase synthesis of azapeptides possessing a C-terminal aza-residue has been accomplished by a protocol featuring regioselective alkylation of benzhydrylidene-aza-glycinamide and illustrated ...

Preclinical evaluation of a high-affinity 18F-trifluoroborate octreotate derivative for somatostatin receptor imaging.

J. Nucl. Med. 55(9) , 1499-505, (2014)

Recent studies have highlighted the high sensitivity of PET imaging with (68)Ga-labeled octreotide derivatives for the detection and staging of neuroendocrine tumors. A somatostatin receptor ligand th...

Related Compounds

The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.