29 Results for "

hCAI/II-IN-6

" in MedChemExpress (MCE) Product Catalog:
Products (29)

29 Results for "hCAI/II-IN-6" in MCE Product Catalog:

2
2 Cited Publications
Cat. No.: HY-130538
CAS No.: 6953-61-3
Purity:  99.72%
Target:  

HDAC

Research Areas:  

Cancer

1-Naphthohydroxamic acid (Compound 2) is a potent and selective HDAC8 inhibitor with an IC50 of 14 μM. 1-Naphthohydroxamic acid is more selectively for HDAC8 than class I HDAC1 and class II HDAC6 (IC50 >100 μM). 1-Naphthohydroxamic acid does not increase global histone H4 acetylation and also does not reduce total intracellular HDAC activity .1-Naphthohydroxamic acid can induce tubulin acetylation .
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1
1 Cited Publications
Cat. No.: HY-B1471
CAS No.: 3801-06-7
Target:  

Carbonic Anhydrase

Research Areas:  

Inflammation/Immunology

Fluorometholone acetate is a synthetic glucocorticoid corticosteroid and a corticosteroid ester. Fluorometholone acetate potently inhibits carbonic anhydrase (CA) with IC50s of 2.18 μM and 17.5 μM for hCA-I and hCA-II, respectively. Fluorometholone acetate has anti-inflammatory effect and has the potential for external ocular inflammation research .
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Cat. No.: HY-69085
CAS No.: 186407-74-9
4-Bromo-1H-indazole is a carbonic anhydrase inhibitor, with an IC50 of 0.403 mM and a Ki of 0.383 mM against hCA-I, as well as an IC50 of 0.700 mM and a Ki of 0.935 mM against hCA-II. 4-Bromo-1H-indazole reduces the catalytic activity of human I and II isoforms of carbonic anhydrase .
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Cat. No.: HY-P1829A
Target:  

Angiotensin Receptor

Research Areas:  

Cardiovascular Disease

Angiotensin I/II (1-6) TFA contains the amino acids 1-6 and is converted from Angiotensin I/II peptide. The precursor angiotensinogen is cleaved by renin to form angiotensin I. Angiotensin I ishydrolyzed by angiotensin-converting enzyme (ACE) to form the biologically active angiotensin II. Angiotensin II has been investigated for the treatment, basic science, and diagnostic of Hypertension, Renin Angiotensin System, and Idiopathic Membranous Nephropathy .
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Cat. No.: HY-P1829
CAS No.: 47896-63-9
Target:  

Angiotensin Receptor

Research Areas:  

Cardiovascular Disease

Angiotensin I/II 1-6 contains the amino acids 1-6 and is converted from Angiotensin I/II peptide. The precursor angiotensinogen is cleaved by renin to form angiotensin I. Angiotensin I ishydrolyzed by angiotensin-converting enzyme (ACE) to form the biologically active angiotensin II. Angiotensin II has been investigated for the treatment, basic science, and diagnostic of Hypertension, Renin Angiotensin System, and Idiopathic Membranous Nephropathy .
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Cat. No.: HY-175847
Target:  

Carbonic Anhydrase

Research Areas:  

Cancer

hCA-I/ HCA-II-IN-2 (compound 5 k) is an effective inhibitor of human carbonic anhydrase I (hCA-I) and II (hCA-II). The IC50 for hCA I and hCA II are 89.25 and 54.50 nM respectively .
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Cat. No.: HY-175972
Target:  

Carbonic Anhydrase

Research Areas:  

Neurological Disease Cancer

CAI/II-IN-12 is a potent and hCAI (IC50 = 7.12 μM, Ki = 9.26 μM) and hCAII (IC50 = 10.62 μM, Ki = 11.72 μM) dual inhibitor. CAI/II-IN-12 has a strong affinity for the active sites of CYP17A1, hCAI, and hCAII enzymes. Compound CAI/II-IN-12 exhibits rapid conformational stabilization, particularly in the CYP17A1 complex. CAI/II-IN-12 can be used for the study of prostate cancer therapy and glaucoma .
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Cat. No.: HY-W306065
CAS No.: 100142-87-8
Target:  

Carbonic Anhydrase

Research Areas:  

Cancer

hCAI/II/XII-IN-1 (compound 7) is a human carbonic anhydrase hCAI/II/XII inhibitor, with Ki values of 78.5, 9.1, 605, 7.7 and 3.7 nM .
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Cat. No.: HY-152041S
CAS No.: 1014689-15-6
Synonyms: Sudan orange RPA-d6; Sudan red II-d6
Sudan II-d6 (Sudan orange RPA-d6) is the deuterium labeled Sudan II (HY-D0928).
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Cat. No.: HY-148135
CAS No.: 694466-00-7
Purity:  ≥98.0%
Target:  

Carbonic Anhydrase

Research Areas:  

Neurological Disease

CAI/II-IN-6 is an orally active human carbonic anhydrase (hCA) inhibitor. CAI/II-IN-6 selectively inhibits hCA II and hCA VII isoforms with Ki values of 220, 4.9, 6.5 and >50000 nM for hCA I, hCA II , hCA VII and hCA XII respectively. CAI/II-IN-6 shows anticonvulsant activity and anti maximal electroshock (MES) activity in vivo. CAI/II-IN-6 can be used for the research of epilepsy .
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Cat. No.: HY-149301
CAS No.: 2925261-76-1
Purity:  98.52%
Target:  

Carbonic Anhydrase

Research Areas:  

Cancer

hCAIX-IN-18 (compound 30) is an inhibitor of carbonic anhydrase (CA), with Kis of 3.5 nM, 9.4 nM, 43.0 nM and 8.2 nM for hCAI, hCAII, hCAIX, hCAXII, respectively. hCAIX-IN-18 can be used for cancer research .
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Cat. No.: HY-147662
CAS No.: 2451479-57-3
Target:  

Carbonic Anhydrase

Research Areas:  

Cancer

hCAIX-IN-5 (compound 6b) is a potent and selective hCAIX inhibitor with KIs of >10000, >10000, 130.7, 829.1 nM for hCAI, hCAII, hCAIV, hCAIX, respectively .
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Cat. No.: HY-146256
CAS No.: 2414629-92-6
Target:  

Carbonic Anhydrase

Research Areas:  

Cancer

hCAXII-IN-5 (compound 6o) is a potent and selective hCAXII inhibitor with Ki values of >10000, >10000, 286.1, 1.0 nM for hCAI, hCAII, hCAIX and hCAXII, respectively .
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Cat. No.: HY-146257
CAS No.: 2414629-82-4
Target:  

Carbonic Anhydrase

Research Areas:  

Cancer

hCAIX/XII-IN-2 (compound 6a) is a potent and selective hCAIX and hCAXIIinhibitor with Ki values of >10000, >10000, 30.0, 3.6 nM for hCAI, hCAII, hCAIX and hCAXII, respectively .
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Cat. No.: HY-147665
CAS No.: 2451479-58-4
Target:  

Carbonic Anhydrase

Research Areas:  

Cancer

hCAIX-IN-7 (compound 6c) is a potent and selective hCAIX inhibitor with KIs of >10000, >10000, 43.0, 410.6 nM for hCAI, hCAII, hCAIV, hCAIX, respectively .
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Cat. No.: HY-146258
CAS No.: 2414629-94-8
Target:  

Carbonic Anhydrase

Research Areas:  

Cancer

hCAIX/XII-IN-3 (compound 6q) is a potent and selective hCAIX and hCAXIIinhibitor with Ki values of >10000, >10000, 66.2, 4.4 nM for hCAI, hCAII, hCAIX and hCAXII, respectively .
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Cat. No.: HY-146316
CAS No.: 2987586-62-7
Target:  

Topoisomerase

Research Areas:  

Cancer

Topoisomerase II inhibitor 6 (Compound 5), a tryptanthrin derivative, is a potent and selective inhibitor of topoisomerase II. Topoisomerase II inhibitor 6 exhibits antiproliferative activity on different tumor cell lines. Topoisomerase II inhibitor 6 blocks the cell cycle of CCRF-CEM in the G2 phase and induces DNA DSB. Topoisomerase II inhibitor 6 has the potential for the research of cancer diseases .
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Cat. No.: HY-157321
CAS No.: 14204-32-1
Target:  

Carbonic Anhydrase

Research Areas:  

Neurological Disease

CAI/II-IN-7 (compound 1F) is a potent carbonic anhydrase (CA) inhibitor with Ki values of 23 nM, 44 nM and 20.57 µM for hCA-I, hCA-II and bovine CA, respectively .
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Cat. No.: HY-161143
CAS No.: 3029817-13-5
Carbonic anhydrase/AChE-IN-2 (compound 19) is a selective acetylcholinesterase (AChE) and carbonic anhydrase (CA) inhibitor, with Ei of 5.07 nM, 24.42 nM and 19.95 nM for AChE, hCAI and hCAII, respectively .
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Cat. No.: HY-161322
Target:  

Carbonic Anhydrase

Research Areas:  

Cancer

hCAXII-IN-9 (Compound 3I) is a selective inhibitor of hCAXII with Ki values of 28 nM, 7192.6 nM, 188.6 nM, and >100000 nM for hCAXII, hCAI, hCAII, and hCAIX, respectively. hCAXII-IN-9 can be utilized in antitumor research .
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