H-Ser-Glu-OH

Modify Date: 2024-01-04 14:23:25

H-Ser-Glu-OH structure	Common Name	H-Ser-Glu-OH
	CAS Number	6403-16-3	Molecular Weight	234.20700
	Density	N/A	Boiling Point	N/A
	Molecular Formula	C₈H₁₄N₂O₆	Melting Point	N/A
	MSDS	Chinese USA	Flash Point	N/A

Use of H-Ser-Glu-OH

(S)-2-((S)-2-Amino-3-hydroxypropanamido)pentanedioic acid is a glutamic acid derivative[1].

Name	2-[(2-amino-3-hydroxypropanoyl)amino]pentanedioic acid
Synonym	More Synonyms

Description	(S)-2-((S)-2-Amino-3-hydroxypropanamido)pentanedioic acid is a glutamic acid 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):1793-1144.

Molecular Formula	C₈H₁₄N₂O₆
Molecular Weight	234.20700
Exact Mass	234.08500
PSA	153.44000

Personal Protective Equipment	Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
RIDADR	NONH for all modes of transport
WGK Germany	3
HS Code	2924199090

HS Code	2924199090
Summary	2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Studies on selection blockers. 5. Design, synthesis, and biological profile of sialyl Lewis x mimetics based on modified serine-glutamic acid dipeptides.

J. Med. Chem. 40 , 3534-3541, (1997)

We have rationally designed a sLe(x) mimetic based on molecular modeling, synthesized type II and type II' beta-turn dipeptides (3a,b), and evaluated their biological profiles both in vitro and in viv...

Carbohydrate mimetics and scaffolds: sweet spots in medicinal chemistry.

Future Med. Chem. 2 , 587-599, (2010)

Several glycoprocessing enzymes and glycoreceptors have been recognized as important targets for therapeutic intervention. This concept has inspired the development of important classes of therapeutic...

Studies on selectin blockers. 7. Structure-activity relationships of sialyl Lewis X mimetics based on modified Ser-Glu dipeptides.

J. Med. Chem. 41 , 4279-4287, (1998)

We have previously found that heterochiral fucodipeptides, L-Ser-D-Glu (3a) and D-Ser-L-Glu (3b), exhibited up to 20-100 times more potency than a sialyl Lewis X (sLeX, 1) and a 3'-sulfated Lewis X an...

N-L-Seryl-L-glutaminsaeure

N-L-seryl-L-glutamic acid

Ser-Glu

serylglutamic acid

L-Seryl=>L-glutaminsaeure