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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
79 Results for "
zwitterionic
" in MedChemExpress (MCE) Product Catalog:
Products (79)
79 Results for "zwitterionic" in MCE Product Catalog:
Cat. No.: HY-P11138
Synonyms: Lac705α
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Cat. No.: HY-W105506R
CAS No.: 4337-33-1
Synonyms: s,s-Dimethyl-β-propionic acid thetine (Standard)
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Cat. No.: HY-W013078S
CAS No.: 326495-41-4
Synonyms: DMPE-d54
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1,2-Dimyristoyl-sn-glycero-3-phosphoethanolamine (DMPE)-d54 is the deuterated-labeled 1,2-Dimyristoyl-sn-glycero-3-phosphoethanolamine (DMPE) (HY-W013078). 1,2-Dimyristoyl-sn-glycero-3-phosphoethanolamine (DMPE) is a zwitterionic saturated phosphatidylethanolamine bearing two myristoyl (C14:0) chains, and serves as a model membrane component, a neutral lipid component of lipid nanoparticles, and a cocoa butter crystallization nucleating agent. 1,2-Dimyristoyl-sn-glycero-3-phosphoethanolamine is used in nucleic acid delivery, construction of artificial cell membrane models, and research on urothelial carcinoma .
Cat. No.: HY-W013078R
CAS No.: 998-07-2
Synonyms: DMPE (Standard)
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Cat. No.: HY-W012908S2
CAS No.: 784086-28-8
DL-Proline-d3 is the deuterated-labeled DL-Proline (HY-W012908). DL-Proline is a racemic mixture of D-Proline and L-Proline, belonging to cyclic imino acids with a five-membered ring structure. DL-Proline serves as a key structural unit in peptide synthesis. DL-Proline stabilizes β-turn conformations and affects the secondary structure of peptide segments. DL-Proline exhibits biological activities such as regulating peptide segment conformations and enhancing cyclic peptide stability. DL-Proline can be used in research on diseases related to peptide structure and function, including cancer and bacterial infections .
Cat. No.: HY-N16165
CAS No.: 40811-59-4
Synonyms: 18:3 PC; Dilinolenoylphosphatidylcholine
1,2-Dilinolenoyl-sn-Glycero-3-Phosphatidylcholine (18:3 PC; Dilinolenoylphosphatidylcholine) is a phosphatidylcholine derivative and zwitterionic phospholipid. 1,2-Dilinolenoyl-sn-Glycero-3-Phosphatidylcholine serves as a component of oral liposomal compositions .
Cat. No.: HY-108535R
CAS No.: 75277-39-3
Cat. No.: HY-101850R
CAS No.: 68399-77-9
Cat. No.: HY-161993A
CAS No.: 3043939-19-8
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(αR)-BI-9787 is the epimer of BI-9787 (HY-161993). BI-9787 is a zwitterionic inhibitior for ketohexokinase.
Cat. No.: HY-P3029E
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Phospholipase A2, Naja mossambica mossambica (EC 3.1.1.4) hydrolyzes the β-ester bond of zwitterionic glycerophospholipids. Preferred substrates are phosphatidylcholine, phosphatidylethanolamine, and their plasmalogen analogues.
Cat. No.: HY-P3029D
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Phospholipase A2, Honey bee venom (Apis mellifera) (EC 3.1.1.4) hydrolyzes the β-ester bond of zwitterionic glycerophospholipids. Preferred substrates are phosphatidylcholine, phosphatidylethanolamine, and their plasmalogen analogues.
Cat. No.: HY-P3029C
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Phospholipase A2, Porcine (EC 3.1.1.4) hydrolyzes the β-ester bond of zwitterionic glycerophospholipids. Preferred substrates are phosphatidylcholine, phosphatidylethanolamine, and their plasmalogen analogues. Phosphatidylinositol and phosphatidylserine are also hydrolyzed. Phospholipase A2specifically recognizes the sn-2 acyl bond of phospholipids and catalytically hydrolyzes the bond releasing arachidonic acid and lysophospholipids.
Cat. No.: HY-P3029B
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Phospholipase A2, Streptomyces violaceoruber (EC 3.1.1.4) hydrolyzes the β-ester bond of zwitterionic glycerophospholipids. Preferred substrates are phosphatidylcholine, phosphatidylethanolamine, and their plasmalogen analogues. Phosphatidylinositol and phosphatidylserine are also hydrolyzed. Phospholipase A2specifically recognizes the sn-2 acyl bond of phospholipids and catalytically hydrolyzes the bond releasing arachidonic acid and lysophospholipids.
Cat. No.: HY-P11820
Cat. No.: HY-W700634
CAS No.: 3025668-93-0
Cat. No.: HY-113278R
CAS No.: 3063-05-6
Cat. No.: HY-W002038R
CAS No.: 56613-80-0
Synonyms: D-Phenylglycinol (Standard); (-)-Phenylglycinol (Standard)
(R)-(-)-2-Phenylglycinol (Standard) (D-Phenylglycinol (Standard); (-)-Phenylglycinol (Standard)) is the analytical standard of (R)-(-)-2-Phenylglycinol (HY-W002038). This product is intended for research and analytical applications. (R)-(-)-2-Phenylglycinol (D-Phenylglycinol; (-)-Phenylglycinol) is a chiral β-amino alcohol, a starting material for chiral synthesis, and a potential nematicide. (R)-(-)-2-Phenylglycinol exhibits nematicidal and egg hatching inhibitory activity against the southern root-knot nematode (Meloidogyne incognita), and is also an upregulated metabolite in the fermentation broth of Streptomyces aquilus JXGZ01. (R)-(-)-2-Phenylglycinol can be used as a framework for constructing zwitterionic bicyclic lactams and multi-substituted piperidine/piperidine acid drugs. (R)-(-)-2-Phenylglycinol can be used in drug synthesis and nematode infection-related research .
Cat. No.: HY-W012908S1
CAS No.: 282729-06-0
DL-Proline-2-d1 is the deuterated-labeled DL-Proline (HY-W012908). DL-Proline is a racemic mixture of D-Proline and L-Proline, belonging to cyclic imino acids with a five-membered ring structure. DL-Proline serves as a key structural unit in peptide synthesis. DL-Proline stabilizes β-turn conformations and affects the secondary structure of peptide segments. DL-Proline exhibits biological activities such as regulating peptide segment conformations and enhancing cyclic peptide stability. DL-Proline can be used in research on diseases related to peptide structure and function, including cancer and bacterial infections .
Cat. No.: HY-203862
CAS No.: 125275-25-4
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Polyquaternium-51 is a hydrophilic polymeric zwitterion with counter ions, and an artificial cell membrane-mimicking material with high biocompatibility. Polyquaternium-51 functions as a penetration inhibitor and exfoliation efficacy reducer. Polyquaternium-51 can be used as cosmetic moisturizing ingredient, and can be used as coating biological scaffolds .
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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
