55 Results for "

TAP

" in MedChemExpress (MCE) Product Catalog:
Products (55)

55 Results for "TAP" in MCE Product Catalog:

5
5 Cited Publications
Cat. No.: HY-134955
CAS No.: 2290608-13-6
Purity:  99.64%
Target:  

YAP

Research Areas:  

Cancer

VT103, an analog of VT101, is an orally active and selective TEAD1 protein palmitoylation inhibitor. VT103 inhibits YAP/TAZ-TEAD promoted gene transcription, blocks TEAD auto-palmitoylation, and disrupts interaction between YAP/TAZ and TEAD. VT103 can be used for the research of cancer .
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1
1 Cited Publications
Cat. No.: HY-W176199
CAS No.: 3421-08-7
DPPD-Q is a quinone derivative of p-phenylenediamine antioxidants and an analog of DTPD-Q (HY-163650). DPPD-Q is identified as a major sewage treatment plant effluent .
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Cat. No.: HY-14751
CAS No.: 552292-08-7
Purity:  99.89%
Synonyms: SCH619734
Target:  

Neurokinin Receptor

Research Areas:  

Neurological Disease

Rolapitant (SCH619734) is a potent, selective, long-acting and orally active neurokinin 1 (NK1) receptor antagonist with a Ki of 0.66 nM. Rolapitant does not interact with CYP3A4. Rolapitant shows potent anti-emetic activity in a ferret emesis model .
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Cat. No.: HY-16436
CAS No.: 914462-92-3
Synonyms: SCH619734 hydrochloride hydrate
Target:  

Neurokinin Receptor

Research Areas:  

Neurological Disease Cancer

Rolapitant hydrochloride hydrate (SCH619734 hydrochloride hydrate) is a potent, selective, long-acting and orally active neurokinin 1 (NK1) receptor antagonist with a Ki of 0.66 nM. Rolapitant hydrochloride hydrate does not interact with CYP3A4. Rolapitant hydrochloride hydrate shows potent anti-emetic activity in a ferret emesis model .
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Cat. No.: HY-158684
CAS No.: 3049076-98-1
Purity:  99.86%
Research Areas:  

Cancer

YX-02-030 is a VHL-dependent MDM2 PROTAC degrader with a Kd of 35 nM. YX-02-030 recruits the VHL E3 ligase to form a ternary complex, leading to ubiquitination and proteasome-mediated degradation of MDM2. YX-02-030 inhibits MDM2-p53 and VHL-HIF1α binding with IC50 values of 63 and 1350 nM. YX-02-030 activates TAp73, upregulates p53 family target genes and induces apoptosis. YX-02-030 demonstrates on-target efficacy in TNBC xenograft-bearing mice, extending survival without normal cell toxicity .
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Cat. No.: HY-P1192
CAS No.: 133156-06-6
Target:  

Neurokinin Receptor

Research Areas:  

Neurological Disease

GR-73632 is a tachykinin NK1 receptor agonist. GR-73632 activates spinal NK1 receptors to induce scratching, biting and licking behaviors. GR-73632 activates peripheral NK1 receptors to trigger lacrimation in guinea pigs, and activates central NK1 receptors to induce repetitive hind paw tapping behavior in gerbils. GR-73632 is applicable to research related to pruritus .
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Cat. No.: HY-14826
CAS No.: 166741-91-9
Synonyms: AVE8112
Research Areas:  

Neurological Disease

Tilivapram (AVE8112) is an orally active PDE4 inhibitor with procognitive effects. Tilivapram exhibits in vivo efficacy and improves processing speed and psychomotor speed. Oral administration of tilivapram may induce dose-related adverse reactions such as nausea and dizziness, but transdermal delivery enables slow, controlled elevation of plasma concentrations, thereby significantly reducing gastrointestinal discomfort and dizziness. Tilivapram is applicable to research related to neuropsychiatric disorders .
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Cat. No.: HY-143695
CAS No.: 139984-36-4
16:0 TAP is a lipid product. 16:0 TAP can be used for the preparation of giant unilamellar vesicles to deliver agents .
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Cat. No.: HY-107997
CAS No.: 1149362-88-8
Target:  

CETP

Research Areas:  

Cardiovascular Disease

TAP311 is a cholesteryl ester transfer protein (CETP) inhibitor with an IC50 of 62 nM .
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Cat. No.: HY-129448
CAS No.: 825643-56-9
Target:  

Neurokinin Receptor

Research Areas:  

Neurological Disease

RO4583298 is a potent, orally active dual antagonist of NK1 (human and gerbil)/NK3 (human, cynomolgus monkey, gerbil and guinea-pig). RO4583298 inhibits senktide-induced potentiation of spontaneous activity of dopaminergic neurons. RO4583298 can block gerbil foot tapping response and inhibits mouse tail whips .
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Cat. No.: HY-P5865
Synonyms: Theraphotoxin-TAP1a; TRTX-TAP1a; µ/ω-TRTX-TAP1a
Target:  

Sodium Channel

Research Areas:  

Neurological Disease

Tap1a (Theraphotoxin-Tap1a) is a spider venom peptide that inhibits sodium channels with IC50s of 80 nM and 301 nM against Nav1.7 and Nav1.1, respectively. Tap1a shows analgesic effects .
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Cat. No.: HY-157051
Target:  

Photosensitizer

Research Areas:  

Cancer

[Ru(DIP)2TAP]Cl2, Ruthenium(II) polypyridyl compound, is a photosensitizer. [Ru(DIP)2TAP]Cl2 can be used for the research of photodynamic therapy (PDT) .
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Cat. No.: HY-RS14201
Research Areas:  

Others

TAP1 Human Pre-designed siRNA Set A contains three designed siRNAs for TAP1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS14202
Research Areas:  

Others

TAP2 Human Pre-designed siRNA Set A contains three designed siRNAs for TAP2 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS18500
Research Areas:  

Others

Tap2 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Tap2 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS24053
Research Areas:  

Others

Tap1 Rat Pre-designed siRNA Set A contains three designed siRNAs for Tap1 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS24982
Research Areas:  

Others

Tap2 Rat Pre-designed siRNA Set A contains three designed siRNAs for Tap2 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS09710
Research Areas:  

Others

NXF1 Human Pre-designed siRNA Set A contains three designed siRNAs for NXF1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-156372
CAS No.: 2758685-58-2
Target:  

Cholinesterase (ChE)

Research Areas:  

Neurological Disease

AChE-IN-44 (Compound Tap4) is an AChE inhibitor. AChE-IN-44 can be converted into the thiazole salt AChE inhibitor Tat2 .
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Cat. No.: HY-RS15519
Research Areas:  

Others

USO1 Human Pre-designed siRNA Set A contains three designed siRNAs for USO1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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