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S3638

Ser-Glu

Name: Ser-Glu
Brand: SIGMA

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About This Item

Empirische Formel (Hill-System):

C₈H₁₄N₂O₆

CAS-Nummer:

6403-16-3

Molekulargewicht:

234.21

MDL-Nummer:

MFCD00063352

UNSPSC-Code:

12352200

PubChem Substanz-ID:

24899565

Lagertemp.

−20°C

SMILES String

NC(CO)C(=O)NC(CCC(O)=O)C(O)=O

InChI

1S/C8H14N2O6/c9-4(3-11)7(14)10-5(8(15)16)1-2-6(12)13/h4-5,11H,1-3,9H2,(H,10,14)(H,12,13)(H,15,16)

InChIKey

LAFKUZYWNCHOHT-UHFFFAOYSA-N

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

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Carbohydrate mimetics and scaffolds: sweet spots in medicinal chemistry.

Laura Cipolla et al.

Future medicinal chemistry, 2(4), 587-599 (2011-03-24)

Several glycoprocessing enzymes and glycoreceptors have been recognized as important targets for therapeutic intervention. This concept has inspired the development of important classes of therapeutics, such as anti-influenza drugs inhibiting influenza virus neuraminidase, anti-inflammatory drugs targeting lectin-sialyl-Lewis X interaction and

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

T Tsukida et al.

Journal of medicinal chemistry, 41(22), 4279-4287 (1998-10-23)

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 analogue (2) toward E-selectin binding and have also proposed

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

T Tsukida et al.

Journal of medicinal chemistry, 40(22), 3534-3541 (1997-11-14)

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 vivo. Against E-selectin-sLe(x) binding, the type II beta-turn dipeptide L-Ser-D-Glu

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