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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
149 Results for "
HD
" in MedChemExpress (MCE) Product Catalog:
Products (149)
149 Results for "HD" in MCE Product Catalog:
7
Target:
Research Areas:
Cystamine is the disulfide form of the free thiol, cysteamine. Cystamine is an orally active transglutaminase (Tgase) inhibitor. Cystamine also has inhibition activity for caspase-3 with an IC50 value of 23.6 μM. Cystamine can be used for the research of severals diseases including Huntington's disease (HD) .
7
7 Publications Verification
Cat. No.: HY-W020050
CAS No.: 56-17-7
Target:
Research Areas:
Cystamine (dihydrochloride) is the disulfide form of the free thiol, cysteamine. Cystamine is an orally active transglutaminase (Tgase) inhibitor. Cystamine also has inhibition activity for caspase-3 with an IC50 value of 23.6 μM. Cystamine can be used for the research of severals diseases including Huntington's disease (HD) .
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4
Target:
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Ropinirole (SKF 101468) hydrochloride is an orally active, potent D3/D2 receptor agonist with a Ki of 29 nM for D2 receptor. Ropinirole hydrochloride has pEC50s of 7.4, 8.4 and 6.8 for hD2, hD3 and hD4 receptors, respectively. Ropinirole hydrochloride has no affinity for the D1 receptors. Ropinirole hydrochloride has the potential for Parkinson's disease .
4
Target:
Research Areas:
Ropinirole (SKF 101468) is an orally active, potent D3/D2 receptor agonist with a Ki of 29 nM for D2 receptor. Ropinirole has pEC50s of 7.4, 8.4 and 6.8 for hD2, hD3 and hD4 receptors, respectively. Ropinirole has no affinity for the D1 receptors. Ropinirole has the potential for Parkinson's disease .
4
4 Cited Publications
Cat. No.: HY-16482
CAS No.: 250694-07-6
4
4 Cited Publications
Cat. No.: HY-P70535
Purity: ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: LGALS9; Ecalectin; Galectin 9; Gal-9; LGALS9A; Urate Transporter/Channel Protein; Lectin, Galactoside-Binding, Soluble, 9; Galectin; Tumor Antigen HOM-HD-21; HUAT; Galectin-9
Species:
Human
Source:
HEK293
3
3 Cited Publications
Cat. No.: HY-P72637
Purity: ≥ 85%, as determined by reducing SDS-PAGE.
Synonyms: LGALS9; Ecalectin; Galectin 9; Gal-9; LGALS9A; Urate Transporter/Channel Protein; Lectin, Galactoside-Binding, Soluble, 9; Galectin; Tumor Antigen HOM-HD-21; HUAT; Galectin-9
Species:
Mouse
Source:
E. coli
2
Research Areas:
Chlorprothixene is a dopamine and histamine receptors antagonist with Kis of 18 nM, 2.96 nM, 4.56 nM, 9 nM and 3.75 nM for hD1, hD2, hD3, hD5 and hH1 receptors, respectively. Antipsychotic activity .
2
Research Areas:
Chlorprothixene hydrochloride is a dopamine and histamine receptors antagonist with Kis of 18 nM, 2.96 nM, 4.56 nM, 9 nM and 3.75 nM for hD1, hD2, hD3, hD5 and hH1 receptors, respectively. Antipsychotic activity .
2
2 Cited Publications
Target:
Research Areas:
GR 103691 is a potent, selective dopamine D3 receptor antagonist with a Ki value of 0.4 nM. GR 103691 shows more than 100-fold selectivity for human dopamine human (h)D3 over hD4 and hD1 sites .
2
2 Cited Publications
Cat. No.: HY-P72262
Purity: ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: HDAC1; GON-10; Prev. RPD3L1; Reduced Potassium Dependency, Yeast Homolog-Like 1; HD1; Protein Decrotonylase HDAC1; Protein Deacetylase HDAC1; Histone Deacetylase; Protein Deacylase HDAC1; RPD3; Histone Deacetylase 1; KDAC1
Species:
Human
Source:
E. coli
1
1
1
1 Cited Publications
Cat. No.: HY-P72224
Purity: ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: HDAC6; HD6; Histone Deacetylase 6; Protein Phosphatase 1, Regulatory Subunit 90; Tubulin-Lysine Deacetylase HDAC6; E3 Ubiquitin-Protein Ligase HDAC6; Protein Deacetylase HDAC6; Alpha-Tubulin Deacetylase HDAC6; KIAA0901; FLJ16239; PPP1R90; HDAC6 Protein; K
Species:
Human
Source:
E. coli
1
1
1 Cited Publications
Target:
Research Areas:
NKL 22 is a potent and selective inhibitor of histone deacetylases (HDAC), with IC50 values of 199 and 69 nM for HDAC1 and HDAC3, respectively. NKL 22 can reverse abnormal expression of HD‑related genes and restore the levels of key genes including Ppp1r1b in Huntington's disease transgenic mice. NKL 22 can be used for the researches of Huntington's disease and cancer .
1
Research Areas:
HD-TAC7 is a selective HDAC3 PROTAC degrader with an IC50 of 1.1 μM. By recruiting the CRBN E3 ligase, HD-TAC7 induces ubiquitin-proteasome degradation and selective downregulation of HDAC3, which in turn increases H3K27 acetylation levels and downregulates the NF-κB subunit p65, exerting anti-inflammatory activity. HD-TAC7 is used in research on COVID-19, SARS-CoV-2 infection, asthma, chronic obstructive pulmonary disease, and colon cancer .
Research Areas:
Hexane-2,5-dione (2,5-HD) is an orally active, CNS-penetrant cytotoxic agent . Hexane-2,5-dione reduces BCL-2 and β-catenin/TCF transcriptional activity, increases BAX and active caspase-3 expression, and promotes apoptosis. Hexane-2,5-dione causes an accumulation of neurofilaments within axons in rats. Hexane-2,5-dione can be used for the research of neurodegenerative diseases .
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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
