35 Results for "

hCAI/II-IN-8

" in MedChemExpress (MCE) Product Catalog:
Products (35)

35 Results for "hCAI/II-IN-8" in MCE Product Catalog:

2
2 Cited Publications
Cat. No.: HY-P1515A
Angiotensin II (3-8), human (TFA) is a less effective agonist at the angiotensin AT1 receptor.
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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-P1769
CAS No.: 34233-50-6
Target:  

Angiotensin Receptor

Research Areas:  

Metabolic Disease Endocrinology

Angiotensin II (5-8), human is an endogenous C-terminal fragment of the peptide vasoconstrictor angiotensin II . Angiotensin II binds the AT II type 1 (AT1) receptor, stimulating GPCRs in vascular smooth muscle cells and increasing intracellular Ca 2+ levels. Angiotensin II also acts at the Na +/H + exchanger in the proximal tubules of the kidney .
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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-120994B
CAS No.: 129693-13-6
Target:  

PKA

Sp-8-CPT-cAMPS, a cAMP analog, is a potent and selective activator of the cAMP-dependent protein kinas A (PKA I and PKA II). Sp-8-CPT-cAMPS selects site A of RI compares to site A of RII by 153-fold and site B of RII compares to site B of RI by 59-fold .
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Cat. No.: HY-P2643
CAS No.: 52530-60-6
Target:  

Endogenous Metabolite

Research Areas:  

Cardiovascular Disease

Angiotensin I/II (4-8), a major metabolite of Angiotensin II, is a C-terminal 4-8 pentapeptide .
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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-P1515
CAS No.: 12676-15-2
Angiotensin II (3-8), human is a less effective agonist at the angiotensin AT1 receptor.
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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-163756
CAS No.: 2769903-01-5
Research Areas:  

Inflammation/Immunology

NLRP3-IN-43 (compound II-8) is a poteny inhibitor of NLRP3 inflammasome activation that binds to the LRR domain, and disrupts NLRP3-NEK7 interaction .
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Cat. No.: HY-120994A
CAS No.: 129735-01-9
Target:  

PKA

Rp-8-CPT-cAMPS, a cAMP analog, is a potent and competitive antagonist of cAMP-induced activation of cAMP-dependent PKA I and II. Rp-8-CPT-cAMPS preferentially selects site A of RI compares to site A of RII and site B of RII compares to site B of RI .
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Cat. No.: HY-149492
CAS No.: 2889356-55-0
Target:  

Phosphatase Fungal

Research Areas:  

Infection

Phosphatase-IN-1 (compound II-8), a propranolol (HY-B0573B) derivative, is a phosphatidate phosphatase (Pah) inhibitor. Phosphatase-IN-1 can binds to MoPah1, with an affinity constant of 19.8 μM. Phosphatase-IN-1 inhibits growth of plant pathogens and shows anti-fungal ability. Phosphatase-IN-1 is not toxic to rice seedlings and wheat heads .
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Cat. No.: HY-161507
CAS No.: 3036136-18-9
CAI/II-IN-8 (Compound 8) is a hydrazide derivative based on 4-hydroxybenzaldehyde. CAI/II-IN-8 primarily targets human carbonic anhydrase isomerase I (hCA I) and II (hCA II) for inhibition (IC50 = 21.35 ± 0.39 nM (CA I); 7.12 ± 0.12 nM (CA II)). CAI/II-IN-8 inhibits AChE and BChE as well(IC50 = 46.27 ±0.75 nM (AChE); 43.38 ± 0.83 nM (BChE)). . .
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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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