13 Results for "

RIN1

" in MedChemExpress (MCE) Product Catalog:
Products (13)

13 Results for "RIN1" in MCE Product Catalog:

10
10 Cited Publications
Cat. No.: HY-137471
CAS No.: 2682114-39-0
Purity:  99.80%
Synonyms: RIN1
Target:  

Notch

Research Areas:  

Cancer

RBPJ Inhibitor-1 (RIN1), the first RBPJ inhibitor, blocks the functional interaction of RBPJ with SHARP. RBPJ Inhibitor-1 (RIN1) inhibits NOTCH-dependent tumor cell proliferation [1].
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1 Cited Publications
Cat. No.: HY-101774
CAS No.: 2095849-04-8
Purity:  98.11%
Target:  

c-Fms

Research Areas:  

Cancer

CSF1R-IN-1 is a CSF1R inhibitor with an with an IC50 of 0.5 nM.
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Cat. No.: HY-RS11982
Research Areas:  

Others

RIN1 Human Pre-designed siRNA Set A contains three designed siRNAs for RIN1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS17055
Research Areas:  

Others

Rin1 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Rin1 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS23499
Research Areas:  

Others

Rin1 Rat Pre-designed siRNA Set A contains three designed siRNAs for Rin1 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-149014
CAS No.: 2639148-08-4
Research Areas:  

Neurological Disease

OX2R-IN-1 (compound 15) is a low cytotoxicity profile OX2R-IN-1 antagonist (a potential OX2R binder) with an IC50 value of 484 μM. OX2R-IN-1 (compound 15) can cross the BBB into the brain with a short half-life [1].
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Cat. No.: HY-149358
CAS No.: 2854331-14-7
Target:  

Neurokinin Receptor

Research Areas:  

Endocrinology

NK3R-IN-1 (compound 16x), a imidazolepiperazine derivative, is an orally active Neurokinin Receptor NK3R inhibitor. NK3R-IN-1 decreases blood luteinizing hormone levels in ovariectomy (OVX) model [1].
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Cat. No.: HY-176405
Target:  

Sigma Receptor

Research Areas:  

Neurological Disease

σ1R-IN-1 ((R,R)-1a) is a potent σ-1R inhibitor with an IC50 of 110 nM. σ1R-IN-1 is promising for research of neuropsychiatric disorders [1].
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Cat. No.: HY-100328
CAS No.: 1257555-79-5
Target:  

Cannabinoid Receptor

Research Areas:  

Neurological Disease

CB2R-IN-1 is a potent cannabinoid CB2 receptor inverse agonist with a Ki of 0.9 nM.
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Cat. No.: HY-159941
CAS No.: 2200453-71-8
Target:  

α-synuclein

Research Areas:  

Neurological Disease

tau-0N4R-IN-1 (Compound 6T) is an BBB-penetrable inhibitor of tau 0N4R oligomerization. tau-0N4R-IN-1 effectively inhibits the fibrosis of tau 0N4R, 2N3R, and 2N4R, exhibits an anti-seeding effect on tau in vitro, reduces the oligomerization of α-syn dose-dependently, and prevents formation of α-syn inclusions. tau-0N4R-IN-1 is stable in mouse microsomes and reduces plaques in brain tissues from AD patients. tau-0N4R-IN-1 has good pharmacokinetic properties in mice [1].
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Cat. No.: HY-170687
CAS No.: 2896132-06-0
Target:  

Angiotensin Receptor

Research Areas:  

Neurological Disease

AT2R-IN-1 (A-174) is a AT2R inhibitor, used in the research of neuropathic pain [1].
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Cat. No.: HY-162062
Target:  

EGFR

Research Areas:  

Cancer

EGFR WT/T790M/L858R-IN-1 (compound 10d) is a potent EGFR inhibitor, with IC50s of 0.097, 0.280, and 0.051?μM for EGFR WT, EGFR T790M, and EGFR L858R, respectively. EGFR WT/T790M/L858R-IN-1 can be used for the research of cancer [1].
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Cat. No.: HY-101774R
CAS No.: 2095849-04-8
Research Areas:  

Cancer

CSF1R-IN-1 (Standard) is the analytical standard of CSF1R-IN-1 (HY-101774). This product is intended for research and analytical applications. CSF1R-IN-1 is a CSF1R inhibitor with an with an IC50 of 0.5 nM.
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