19 Results for "

ANOS1

" in MedChemExpress (MCE) Product Catalog:
Products (19)

19 Results for "ANOS1" in MCE Product Catalog:

6
6 Publications Verification
Cat. No.: HY-105917
CAS No.: 265646-85-3
Purity:  99.41%
Synonyms: Endovion; NS3728
Target:  

Chloride Channel

Research Areas:  

Others

Endovion is a pharmacological anion channel inhibitor (like chloride channel) and the specific VRAC/VSOAC blocker. Endovion (NS3728) is also an Anoctamin-1 (ANO 1) channel inhibitor [1] .
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3
3 Cited Publications
Cat. No.: HY-100612
CAS No.: 552309-42-9
Purity:  ≥99.0%
Target:  

Chloride Channel

Research Areas:  

Others

T16Ainh-A01, an aminophenylthiazole, is a potent transmembrane protein 16A (TMEM16A) inhibitor, inhibiting TMEM16A-mediated chloride currents with an IC50 value of ~1 µM. TMEM16A (ANO1) functions as a calcium-activated chloride channel (CaCC) [1] .
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2
2 Cited Publications
Cat. No.: HY-119981
CAS No.: 356102-14-2
Purity:  99.12%
Target:  

Chloride Channel

Research Areas:  

Neurological Disease Cancer

Ani9 is an ANO1 inhibitor, with an IC50 of 77 nM. Ani9 can inhibit smooth muscle contractions in mice and is applicable in research related to diseases such as tumors [1] .
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2
2 Cited Publications
Cat. No.: HY-146320
CAS No.: 407587-01-3
Purity:  99.57%
Target:  

Chloride Channel

Research Areas:  

Cancer

ANO1-IN-1 (Compound 9c) is a selective ANO1 channel blocker with an IC50 of 2.56 μM and 15.43 μM against ANO1 and ANO2, respectively. ANO1-IN-1 suppresses strongly proliferation of glioblastoma cells [1].
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1
1 Cited Publications
Cat. No.: HY-N5101
CAS No.: 36150-23-9
Kobusin is a bisepoxylignan isolated from the Pnonobio biondii Pamp. Kobusin is an activator of CFTR and CaCCgie chloride channels and a inhibitor of ANO1/CaCC (calcium-activated chloride channel) channel [1] .
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1
1 Cited Publications
Cat. No.: HY-N4253
CAS No.: 173792-61-5
Kudinoside D is a triterpenoid saponin. Kudinoside D is isolated from the leaves of Ilex kudingcha. Kudinoside D enhances the phosphorylation levels of AMPK and its downstream molecule ACC, and inhibits the expression of PPARγ, C/EBPα, SREBP-1c as well as the target genes of adipogenic transcription factors. Kudinoside D inhibits the activity of ANO1. Kudinoside D possesses hypolipidemic activity. Kudinoside D can be used in obesity-related research [1] .
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Cat. No.: HY-153508
CAS No.: 2098490-06-1
Target:  

Chloride Channel

Research Areas:  

Others

ANO1-IN-4 (Compound 10bm) is a reversible inhibitor for calcium-activated chloride channel transmembrane protein 16A (TMEM16A, also known as ANO1) with an IC50 of 0.030 µM. ANO1-IN-4 exhibits good metabolic stability in rat liver microsomes. ANO1-IN-4 inhibits spontaneous contraction in mouse isolated ileum [1].
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Cat. No.: HY-146334
CAS No.: 2966044-07-3
Purity:  99.25%
DFBTA is an orally active and potent ANO1 (Calcium-activated chloride channel anoctamin-1) inhibitor, with an IC50 of 24 nM. DFBTA shows analgesic efficacy for inflammatory pain [1].
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Cat. No.: HY-RS00750
Research Areas:  

Others

ANOS1 Human Pre-designed siRNA Set A contains three designed siRNAs for ANOS1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-118170
CAS No.: 171506-87-9
Purity:  90
Target:  

Chloride Channel

Research Areas:  

Others

T16A(inh)-C01 is an inhibitor of TMEM16A (ANO1). T16A(inh)-C01 blocks chloride channel mediated by ANO1 with an IC50 of 8.4 μM, without interfering with calcium signaling [1].
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Cat. No.: HY-175669
Target:  

Chloride Channel

Research Areas:  

Metabolic Disease Endocrinology

ANO1-IN-5 is an orally active ANO1 inhibitor with an IC50 of 4.57 μM. J ANO1-IN-5 demonstrates 118-, 642-, and 10000-fold selectivity over α1A-1B-, andα1D-AR, respectively. ANO1-IN-5 exhibits significant inhibitory effects on osteoclast differentiation and function. ANO1-IN-5 can used for the study of osteoporosis [1].
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Cat. No.: HY-147874
CAS No.: 2494280-04-3
Research Areas:  

Cancer

ANO1-IN-3 (Compound 3n) is a potent and selective ANO1 inhibitor with an IC50 of 1.23 μM. ANO1-IN-3 induces apoptosis [1].
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Cat. No.: HY-146321
CAS No.: 637314-12-6
Target:  

Chloride Channel

Research Areas:  

Cancer

ANO1-IN-2 (Compound 10q) is a selective ANO1 channel blocker with an IC50 of 1.75 μM and 7.43 μM against ANO1 and ANO2, respectively. ANO1-IN-2 suppresses strongly proliferation of glioblastoma cells [1].
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Cat. No.: HY-P990337

Target:  

Chloride Channel

Research Areas:  

Inflammation/Immunology

Anti-ANO1/TMEM16A Antibody is a CHO-expressed human antibody that targets ANO1/TMEM16A. The Anti-ANO1/TMEM16A Antibody consists of a huIgG2 heavy chain and a huκ light chain, with a predicted molecular weight (MW) of 150 kDa. The isotype control for the Anti-ANO1/TMEM16A Antibody can refer to Human IgG1 kappa, Isotype Control (HY-P99001).
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Cat. No.: HY-RS00740
Research Areas:  

Others

ANO1 Human Pre-designed siRNA Set A contains three designed siRNAs for ANO1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS23781
Research Areas:  

Others

Ano1 Rat Pre-designed siRNA Set A contains three designed siRNAs for Ano1 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS17326
Research Areas:  

Others

Ano1 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Ano1 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-105917R
CAS No.: 265646-85-3
Synonyms: Endovion (Standard); NS3728 (Standard)
Research Areas:  

Others

Emidurdar (Standard) is the analytical standard of Emidurdar (HY-105917). This product is intended for research and analytical applications. Endovion is a pharmacological anion channel inhibitor (like chloride channel) and the specific VRAC/VSOAC blocker. Endovion (NS3728) is also an Anoctamin-1 (ANO 1) channel inhibitor [1] .
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Cat. No.: HY-100612R
CAS No.: 552309-42-9
Research Areas:  

Others

T16Ainh-A01 (Standard) is the analytical standard of T16Ainh-A01 (HY-100612). This product is intended for research and analytical applications. T16Ainh-A01, an aminophenylthiazole, is a potent transmembrane protein 16A (TMEM16A) inhibitor, inhibiting TMEM16A-mediated chloride currents with an IC50 value of ~1 μM. TMEM16A (ANO1) functions as a calcium-activated chloride channel (CaCC) [1] .
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