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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
78 Results for "
RB 2 para
" in MedChemExpress (MCE) Product Catalog:
Products (78)
78 Results for "RB 2 para" in MCE Product Catalog:
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3
Category:
2
2 Cited Publications
Synonyms: (-)-para-Nitroblebbistatin
para-Nitroblebbistatin is a derivative of Blebbistatin (HY-13813) and an inhibitor of myosin II. para-Nitroblebbistatin is photostable, non-cytotoxic, and non-phototoxic. para-Nitroblebbistatin can serve as an ideal substitute for Blebbistatin (HY-13813) to study the role of myosin II in physiology, development, and cell biology [2].
1
Research Areas:
N6-(4-Hydroxybenzyl) adenosine (Para-topolin riboside) is an equilibrative nucleoside transporter 1 (ENT1) inhibitor and a selective agonist of adenosine A2a receptor (A2aR), and also exhibits activity against P2Y12 receptor. N6-(4-Hydroxybenzyl) adenosine reduces ethanol intake and preference, attenuates operant conditioning-induced ethanol place preference, decreases the value of ethanol-related rewards, and inhibits collagen-induced platelet aggregation. N6-(4-Hydroxybenzyl) adenosine can be used in studies related to alcohol use disorder [2].
1
1 Cited Publications
Cat. No.: HY-P74834
Purity: ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: IL12RB2; IL-12R Subunit Beta-2; Interleukin 12 Receptor Subunit Beta 2; Interleukin-12 Receptor Beta-2 Chain; Interleukin-12 Receptor Subunit Beta-2; IL-12R-Beta-2; Interleukin 12 Receptor, Beta 2; IL-12RB2; IL-12 Receptor Subunit Beta-2
Species:
Mouse
Source:
HEK293
Target:
Research Areas:
Para-aminoblebbistatin is the inhibitor for myosin II. Para-aminoblebbistatin inhibits the ATPase activity of myosin II, thereby blocking the formation and contraction of the actin-myosin network. Para-aminoblebbistatin is a non-fluorescent and photostable Blebbistatin (HY-13813) derivative [2].
Synonyms: 4-Nitrobenzyl mesylate; para-Nitrobenzyl mesylate; PNBM
Target:
Research Areas:
Cardiovascular Disease Neurological Disease Inflammation/Immunology
p-Nitrobenzyl mesylate (4-Nitrobenzyl mesylate) is an alkylating reagent. p-Nitrobenzyl mesylate alkylates thiophosphorylated serine, threonine, tyrosine residues and cysteine thiols, without modifying hydroxyl, amino or carboxylic acid functional groups. p-Nitrobenzyl mesylate generates thiophosphate epitopes on thiophosphorylated substrate proteins for recognition by thiophosphate-specific antibodies. p-Nitrobenzyl mesylate facilitates the identification and purification of kinase substrates. p-Nitrobenzyl mesylate is applicable to studies related to cerebral ischemia-reperfusion injury [2] .
Research Areas:
Sulfalene (Sulfametopyrazine) is an orally active antimalarial agent. Sulfalene competes with para-aminobenzoic acid in plasmodial and bacterial folic acid synthesis pathways. Sulfalene reduces trachoma-associated pathological changes. Sulfalene can be used for the research of acute falciparum malaria, Schistosoma mansoni infection, trachoma, chronic bronchitis, and bacteriuria in pregnancy [2] .
Cat. No.: HY-165836
CAS No.: 17363-90-5
Target:
Research Areas:
Para-nitrophenyl oleate is an ester product.
Cat. No.: HY-N2506
CAS No.: 83459-41-0
Category:
Cardiovascular Disease Triterpenes Plant Terpenoids Panax ginseng C. A. Meyer Extract Disease Research Fields Araliaceae Extract
Target:
Synonyms: paraniazide; Pasiniazide; Isonicotinic acid hydrazide p-aminosalicylate
Pasiniazid is a chemical complex formed by Isoniazid (HY-B0329) and Para-aminosalicylic acid in a 1:1 molar ratio. Pasiniazid is an antibacterial agent. Pasiniazid is rapidly decomposed into isoniazid and para-aminosalicylic acid in the gastrointestinal tract. Isoniazid exerts a bactericidal effect, while para-aminosalicylic acid delays the acetylation process of isoniazid. Pasiniazid has antibacterial activity against Mycobacterium tuberculosis. Pasiniazid can be used in tuberculosis research .
Cat. No.: HY-171702
Research Areas:
8PPD-Q, a para-phenylenediamine quinonec, is a rubber antioxidant. 8PPD-Q has superior antioxidant and anti-ozone activities but is toxic to the aquatic species, especially salmonids. 8PPD-Q can be used for environmental pollution research .
Cat. No.: HY-N0040R
CAS No.: 11021-13-9
Synonyms: Ginsenoside C (Standard)
Target:
Research Areas:
Iptakalim hydrochloride, a lipophilic para-amino compound, is a novel ATP-sensitive potassium channel (KATP) opener, as well as an α4β2-containing nicotinic acetylcholine receptor (nAChR) antagonist .
Cat. No.: HY-G0005
CAS No.: 949095-98-1
Synonyms: para-Naphthol duloxetine
Target:
Research Areas:
Para-Naphthol Duloxetine is a metabolite of Duloxetine, which is a serotonin-norepinephrine reuptake inhibitor (SNRI).
Cat. No.: HY-W145693
CAS No.: 64309-01-9
Target:
Research Areas:
AKOS B018304 is an arylalkylidene derivative, with polar substitution at para-position.
Cat. No.: HY-76547S1
CAS No.: 1219798-76-1
Synonyms: 4-Methylbenzoic acid-d7
Cat. No.: HY-76547S2
CAS No.: 19215-16-8
Synonyms: 4-Methylbenzoic acid-d3
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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
