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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
334 Results for "
hydroxyl groups
" in MedChemExpress (MCE) Product Catalog:
Products (334)
334 Results for "hydroxyl groups" in MCE Product Catalog:
Research Areas:
Methoxyamine hydrochloride (Standard) is the analytical standard of Methoxyamine hydrochloride. This product is intended for research and analytical applications. Methoxyamine (O-Methylhydroxylamine) hydrochloride is an orally active and potent base excision repair (BER) inhibitor. Methoxyamine hydrochloride binds to 3’ hydroxyl groups that are left behind by 3-methylpurine-DNA glycosylase (MPG) following excision of the damaged base and thus inhibits BER activity. Methoxyamine hydrochloride binds directly to the apyrimidinic (AP) sites. Methoxyamine hydrochloride synergistically enhances the therapeutic efficacy of DNA-damaging agents .
Cat. No.: HY-N19720
CAS No.: 22684-08-8
Target:
Cat. No.: HY-W010505S
CAS No.: 6843-76-1
Cat. No.: HY-W047187
CAS No.: 117405-51-3
Target:
Cat. No.: HY-W013222
CAS No.: 55066-53-0
Target:
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(R,Z)-Ethyl 12-hydroxyoctadec-9-enoate is a naturally occurring organic compound belonging to the class of fatty acid esters. It is derived from oleic acid, a common unsaturated fatty acid found in various animal and plant sources. (R,Z)-Ethyl 12-hydroxyoctadec-9-enoate contains an ethyl group and a hydroxyl group at specific positions in the fatty acid chain. It has various applications in industry and biomedicine, especially as a precursor for the synthesis of other bioactive compounds. (R,Z)-Ethyl 12-hydroxyoctadec-9-enoate is also used in the formulation of certain types of cosmetic and personal care products, such as skin creams and lotions.
Cat. No.: HY-Y0850U1
CAS No.: 9002-89-5
Synonyms: Polyvinyl alcohol (Mw 61000, 98-99% hydrolyzed, ~1400 polymerization); Poly(Ethenol) (Mw 61000, 98-99% hydrolyzed, ~1400 polymerization)
Cat. No.: HY-123558
CAS No.: 74141-69-8
Synonyms: Y 14556
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Bactobolin C is an antibiotic produced by Pseudomonas sp. BMG13A7, which has strong antimicrobial and antitumor activities, can also inhibit antibody production and treat autoimmune encephalomyelitis. However, its undesirable toxicity limits its medicinal application. The unique chemical structure and promising biological activities of Bactobolin C have attracted people's interest in its total synthesis and new active analogs. So far, the structural modification of Bactobolin C has mainly focused on the hydroxyl groups on the amino acid side chains and backbone.
Cat. No.: HY-W127711
CAS No.: 14263-94-6
Cat. No.: HY-W145552
CAS No.: 144985-19-3
Synonyms: 4-Methoxyphenyl 3-O-allyl-beta-D-galactopyranoside
Cat. No.: HY-15613A
CAS No.: 1010732-14-5
Synonyms: (-)-Marinopyrrole A
Category:
Synonyms: 4-Nitrophenyl a-D-mannopyranoside
Cat. No.: HY-186146A
CAS No.: 3013618-85-1
Synonyms: SGI-1776-cis-VHL-02
SGI-1776-VHL-02-epimer (SGI-1776-cis-VHL-02) is an epimer control compound of with SGI-1776-VHL-02 (HY-186146). SGI-1776-VHL-02-epimer has an inverted stereocenter in the critical hydroxyl-proline group in the VHL ligand. SGI-1776-VHL-02-epimer cannot trigger the VHL E3 ligase complex and does not degrade PIM1 .
Synonyms: β-CDN3; 6A-deoxy-6A-azido-β-cyclodextrin
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6A-Azido-6A-deoxy-β-cyclodextrin (β-CDN3) is a site-specifically modified β-cyclodextrin with a single azido group replacing the hydroxyl group at the C6 position. 6A-Azido-6A-deoxy-β-cyclodextrin forms a host-guest inclusion complex with Dexamethasone (HY-14648), localizing the drug within its hydrophobic cavity, which restricts the rotational mobility of the drug and places Dexamethasone in a less polar environment. 6A-Azido-6A-deoxy-β-cyclodextrin acts as a coupling agent to graft β-cyclodextrin onto thermosensitive nanogels via strain-promoted alkyne-azide cycloaddition (SPAAC). 6A-Azido-6A-deoxy-β-cyclodextrin also serves as a click chemistry reagent. It contains an azide group and undergoes copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules bearing an alkyne group. It also undergoes strain-driven alkyne-azide cycloaddition (SPAAC) with molecules containing DBCO or BCN groups .
Cat. No.: HY-W011556
CAS No.: 94790-35-9
Synonyms: TCFH
Cat. No.: HY-W105988
CAS No.: 20427-59-2
Research Areas:
Copper dihydroxide is a copper group metal hydroxide molecule with significant covalent character, a planar 2B9 ground-state electronic state, and C2h symmetry .
Cat. No.: HY-W339834
CAS No.: 325465-92-7
Research Areas:
1-Stearoyl-sn-glycerol 3-phosphate sodium is a bioactive phospholipid that plays a crucial role in modulating cellular processes such as motility, proliferation, invasion, survival, and growth factor production, primarily through its interaction with G protein-coupled receptors (GPCRs). Typically found at low concentrations in plasma (~100nM), this compound is synthesized during the formation of membrane phospholipids and is derived from various cell types, including activated platelets, epithelial cells, leukocytes, neuronal cells, and tumor cells. Its unique structure includes stearic acid at the sn-1 position alongside a hydroxyl group at the sn-2 position.
Cat. No.: HY-128417AR
CAS No.: 14431-43-7
Cat. No.: HY-G0004R
CAS No.: 37519-14-5
Synonyms: 3-Hydroxyacetaminophen (Standard)
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Acetaminophen metabolite 3-hydroxy-acetaminophen (3-Hydroxyacetaminophen) (Standard) is the analytical standard of Acetaminophen metabolite 3-hydroxy-acetaminophen (HY-G0004). This product is intended for research and analytical applications. Acetaminophen metabolite 3-hydroxy-acetaminophen is a non-toxic metabolite and antioxidant of acetaminophen (HY-66005) with free radical scavenging activity. Acetaminophen metabolite 3-hydroxy-acetaminophen can reduce oxidative damage by exerting electron donation ability and antioxidant activity through phenolic hydroxyl groups. 3-hydroxy-acetaminophen can be used to study the toxicity mechanism and drug metabolism of acetaminophen .
Cat. No.: HY-W015936
CAS No.: 928-95-0
Synonyms: trans-Hex-2-en-1-ol
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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
