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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
222 Results for "
UDP
" in MedChemExpress (MCE) Product Catalog:
Products (222)
222 Results for "UDP" in MCE Product Catalog:
Cat. No.: HY-E70025
Synonyms: GlcNAc1pUT
N-acetylglucosamine-1-P uridyltransferase (AGX1) (EC 2.3.1.157) (GlcNAc1pUT) is a bifunctional acetyltransferase/uridyltransferase. N-acetylglucosamine-1-P uridyltransferase (AGX1) binds GlcNAc-1-P and UTP, and catalyzes an uridyltransfer reaction to synthesize UDP-GlcNAc. N-acetylglucosamine-1-P uridyltransferase (AGX1) is a bifunctional enzyme exclusive to prokaryotes .
Cat. No.: HY-P5508
CAS No.: 869012-67-9
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Cat. No.: HY-185308
CAS No.: 895525-81-2
Trisaccharides 3 (compoudn 3) is a GlfT2 acceptor substrate with a 50 μM Ka. Trisaccharides 3 acts as an acceptor substrate for the β-(1→6) galactofuranosyl transferase activity of GlfT2, binds competitively at GlfT2’s single active site pocket, and undergoes galactosylation by GlfT2 with UDP-Galf to form a tetrasaccharide product. Trisaccharides 3 can be used for the research of tuberculosis, hiv-associated Mycobacterium avium infections .
Cat. No.: HY-E71259
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Research Areas:
β-1,3-Galactosyl-O-glycosyl-glycoprotein β-1,3-N-acetylglucosaminyltransferase (EC 2.4.1.146) is an enzyme with systematic name UDP-N-acetyl-D-glucosamine:beta-D-galactosyl-(1->3)-(N-acetyl-D-glucosaminyl-(1->6))-N-acetyl-D-galactosaminyl-R 3-beta-N-acetyl-D-glucosaminyltransferase.
Target:
Cat. No.: HY-W415856
CAS No.: 7296-64-2
Synonyms: Beta-D-galactose
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Research Areas:
β-D-galactose (Beta-D-galactose) is one of the two anomers of D-Galactose (HY-N0210). β-D-galactose efficiently binds to and inhibits the galactose repressor (GalR), thereby inducing the expression of the gal regulon. β-D-galactose acts as a persistent induction signal to trigger the synthesis of UDP-galactose for the biosynthetic glycosylation pathway, rather than serving as a carbon source in Yersinia pestis with inactivated GalM .
Cat. No.: HY-E71026
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β-1,4-Galactosyl Transferase, Bovine (EC 2.4.1.22) catalyzes the transfer of galactose from UDP-galactose to the terminal N-acetylglucosamine residues on elongating oligosaccharide chains. β-1,4-Galactosyl Transferase, Bovine (EC 2.4.1.22) can also be found on the cell surface functioning as a cell-adhesion molecule during various cellular interactions by binding to N-acetylglucosamine containing oligosaccharide substrates or ligands in the extracellular matrix.
Cat. No.: HY-N0372R
CAS No.: 58749-22-7
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Cat. No.: HY-P705434
Purity: ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: B3GNT5; Lactotriaosylceramide Synthase; UDP-GlcNAc:BetaGal Beta-1,3-N-Acetylglucosaminyltransferase 5; Lc(3)Cer Synthase; Beta3Gn-T5; Beta-1,3-Gn-T5; Lactosylceramide 1,3-N-Acetyl-Beta-D-Glucosaminyltransferase; Lc3 Synthase; B3GN-T5; BGnT-5; UDP-GlcNAc:B
Species:
Human
Source:
E. coli
Cat. No.: HY-133204R
CAS No.: 71422-67-8
Synonyms: IKI-7899 (Standard)
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Chlorfluazuron (Standard) (IKI-7899 (Standard)) is the analytical standard of Chlorfluazuron (HY-133204). This product is intended for research and analytical applications. Chlorfluazuron (IKI-7899) is a benzoylurea chitin synthesis inhibitor and a PPARγ agonist ligand that blocks the polymerization of UDP-N-acetylglucosamine by inhibiting chitin synthase, disrupting cuticle formation, molting, and embryonic development, thereby exerting ovicidal, larvicidal, and fecundity-reducing effects in insects. Chlorfluazuron is used in hepatotoxicity research .
Cat. No.: HY-E72107
Human UGT1A4 is a UDP-glucuronosyltransferase. Human UGT1A4 is the major enzyme catalyzing the glucuronidation of 25-hydroxyvitamin D3 (HY-32351) in the liver, and maintains vitamin D homeostasis by clearing 25-hydroxyvitamin D3. Human UGT1A4 regulates the substrate-dependent enzymatic activities of UGT1A1 and UGT1A6, while its own activity is also subject to substrate-dependent regulation by co-expressed UGT1A1 and UGT1A6 .
Cat. No.: HY-E72110
Human UGT1A8 is a UDP-glucuronosyltransferase. Human UGT1A8 catalyzes the transfer of glucuronosyl group from UDPGA to Dihydrotestosterone, forming DHT monoglucuronide. Human UGT1A8 catalyzes the transfer of glucuronosyl group from UDPGA to DHT monoglucuronide, introducing a second glucuronosyl group at the C2 ' position of the latter to form DHT diglucuronide. Human UGT1A8 catalyzes the glucuronidation reactions of coumarins, anthraquinones, flavonoids, phenolic compounds, catechol estrogens, primary amines including 4-Aminobiphenyl, and some opioids .
Cat. No.: HY-E72116
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Human UGT2B4 is a UDP-glucuronosyltransferase. UGT2B4 catalyzes the glucuronidation of bile acids, Carvedilol (HY-B0006) and 6-hydroxylated bile acids to form glucuronide derivatives. UGT2B4 participates in the inactivation of endogenous and exogenous substances, including catechol estrogens, C19 steroids, phenols and monoterpenoids. Human UGT2B4 can be used in the research of hypertension, angina pectoris, chronic heart failure and intrahepatic cholestasis .
Cat. No.: HY-P87524
Synonyms: UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit, O-GlcNAc transferase subunit p110, O-linked N-acetylglucosamine transferase 110 kDa subunit, OGT
Cat. No.: HY-N0235R
CAS No.: 10309-37-2
Synonyms: (S)-(+)-Bakuchiol (Standard)
Cat. No.: HY-P705954
Purity: ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: GPR17; UDP/CysLT Receptor; G Protein-Coupled Receptor 17; P2Y-Like Receptor; Uracil Nucleotide/Cysteinyl Leukotriene Receptor; R12; G-Protein Coupled Receptor 17
Species:
Human
Source:
E. coli Cell-free
Cat. No.: HY-P7630
Purity: ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: B4GALT4; Beta-1,4-GalTase 4; Beta-1,4-Galactosyltransferase 4; Nal Synthase; Beta4Gal-T4; B4Gal-T4; UDP-Galactose:Beta-N-Acetylglucosamine Beta-1,4-Galactosyltransferase 4; Beta-N-Acetylglucosaminyl-Glycolipid Beta-1,4-Galactosyltransferase 4; UDP-Gal:Bet
Species:
Human
Source:
HEK293
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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
