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cs 701 cs-706

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    16
    TargetMol | Activity
CS-722 Free base
T10893749179-13-3In house
CS-722 Free base is a synthetic central muscle relaxant exhibiting muscle relaxant effects and inhibition of spinal reflexes. In hippocampal cultures, CS-722 Free base may suppress spontaneous inhibitory and excitatory post-synaptic currents by inhibiting sodium and calcium currents.
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6-8 weeks
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TargetMol | Inhibitor Sale
CS-B1628
tert-Butyl 2-(6-bromo-5-methyl-2,4-dioxo-1,4-dihydrothieno[2,3-d]pyrimidin-3(2H)-yl)-2-methylpropanoate,ACN-053859
T87491434643-33-0
CS-B1628 (tert-Butyl 2-(6-bromo-5-methyl-2,4-dioxo-1,4-dihydrothieno[2,3-d]pyrimidin-3(2H)-yl)-2-methylpropanoate) can be used in the synthesis of pyrimidine derivatives, with the potential use of being a starting material for a wide variety of organic compounds, including pharmaceuticals and agrochemicals.
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CS-0047390
(S)-Di-tert-butyl 2-(3-((S)-6-amino-1-(tert-butoxy)-1-oxohexan-2-yl)ureido)pentanedioate
T92801025796-31-9
CS-0047390, also known as tert-Butyl-DCL, PSMA inhibitor, is a radiopaque peptide reagent.
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CS 2100
1-[[4-Ethyl-5-[5-(4-phenoxyphenyl)-1,2,4-oxadiazol-3-yl]-2-thienyl]methyl]-3-azetidinecarboxylic acid
T22697913827-99-3
CS 2100 (1-[[4-Ethyl-5-[5-(4-phenoxyphenyl)-1,2,4-oxadiazol-3-yl]-2-thienyl]methyl]-3-azetidinecarboxylic acid) is an S1P1 agonist.
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CS-003 HCl
T69852216776-73-7
CS-003 HCl is a TNRA - triple neurokinin receptor antagonist.
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10-14 weeks
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CS-0777
CS0777,CS 0777
T31107840523-39-9
CS-0777 is a potent, selective, and orally active S1P1 agonist (sphingosine 1-phosphate receptor modulator).
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10-14 weeks
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CS-003 Free base
T10892191672-52-3
CS-003 free base (CS-003) is a triple tachykinin receptor antagonist with high affinity for human (neurokinin) NK1, NK2 and NK3 receptors, with Ki values of 2.3 nM and 0.54 nM, respectively And 0.74 nM. CS-003 free base (CS-003) has therapeutic effects on
  • Inquiry Price
10-14 weeks
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CS-6253
T895441627911-44-7
CS-6253 is an agonist of ATP Binding Cassette 1 (ABCA 1). It modulates the amyloid beta Aβ42 40 ratio, influencing lipoprotein metabolism in the plasma. Additionally, CS-6253 promotes the production of cholesterol-rich high-density lipoprotein (HDL) particles and induces the release of microparticles.
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CS-6253 TFA
T89173
CS-6253TFA is the TFA salt form of CS-6253. This compound serves as an activator for the ATP Binding Cassette 1 (ABCA1). It effectively modulates the amyloid-beta Aβ42 40 ratio and influences the metabolism of lipoproteins in plasma. Additionally, CS-6253TFA facilitates the production of cholesterol-rich high-density lipoprotein (HDL) particles and induces the release of microparticles.
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CS 834
UNII-H26S03B779,CS834,CS-834
T31106157542-49-9
CS 834, a novel oral carbapenem antibiotic, is an ester prodrug of the active metabolite R-95867.
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CS 461
CS461,CS-461
T31104115948-58-8
CS 461 is a cephalosporin antibiotic that has shown effective antimicrobial activity against a variety of bacteria in vitro and in vivo.
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CS-526
R-105266,R 105266,R105266
T27092313272-12-7
CS-526 is a proton pump inhibitor. The inhibitory mechanism of CS-526 on H+,K+-ATPase was a competitive antagonism to the K+ binding site of H+,K+-ATPase, and it was also a reversible inhibition. CS-526 has a potent antisecretory effect on gastric acid se
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8-10 weeks
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CS 224
CS-224,CS224
T3110378541-81-8
CS 224 is a bio-active chemical.
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CS-0045569
T719711268024-07-2
CS-0045569, also known ZUN24972, is an important chemical intermediate for drug synthesis. It was reported in WO 2020086857 (compound 27, page 57) as an intermediate for synthesis of WDR5 inhibitor.
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6-8 weeks
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CS 722
CS-722,CS722
T31105144886-17-9
CS 722 is a centrally acting muscle relaxant. CS-722 exerts its muscle relaxant action by affecting both the supraspinal structure and the spinal cord.
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1-2 weeks
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13(S)HODE Ethanolamide
T70017198123-90-9
13(S)HODE Ethanolamide is a biochemical used to inhibit the adhesion of tumor cells
  • Inquiry Price
6-8 weeks
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