- Signaling Pathways
- Metabolic Enzyme/Protease
- Carbonic Anhydrase
Carbonic Anhydrase
Carbonate dehydratase
Carbonic anhydrase (CA) is a zinc-containing enzyme that catalyzes the reversible hydration of carbon dioxide: CO2 + H2O ⇋ HCO3- + H+. Eight genetically distinct carbonic anhydrase enzyme families (α-, β-, γ- δ-, ζ-, η-, θ- and ι- CAs) were described to date. Carbonic anhydrases are involved in numerous physiological and pathological processes. Many of them are important therapeutic targets with the potential to be inhibited to treat a range of disorders including oedema, glaucoma, obesity, cancer, epilepsy, and osteoporosis.
The carbonic anhydrase reaction is involved in many physiological and pathological processes, including respiration and transport of CO2 and bicarbonate between metabolizing tissues and lungs; pH and CO2 homeostasis; electrolyte secretion in various tissues and organs; biosynthetic reactions (such as gluconeogenesis, lipogenesis, and ureagenesis); bone resorption; calcification; and tumorigenicity. α-CAs are Zn2+ metalloproteins expressed in animals, vertebrates, prokaryotes, fungi, algae, protozoa, and plants. Sixteen mammalian α-CA isoforms are known to be involved in many diseases such as glaucoma, edema, epilepsy, obesity, hypoxic tumors, neuropathic pain, arthritis, neurodegeneration, etc.
Carbonic Anhydrase Isoform Specific Products
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Carbonic Anhydrase
(193)
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CA
(7)
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CA I
(68)
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CA Ⅱ
(120)
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CA IX
(106)
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CA XII
(64)
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CA VII
(1)
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CA VI
(2)
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CA VA
(2)
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CA VB
(2)
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CA XIII
(2)
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CA XIV
(2)
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All Product Categories
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Carbonic Anhydrase Inhibitors
(342)
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Carbonic Anhydrase Activators
(6)
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Carbonic Anhydrase Modulators
(4)
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Carbonic Anhydrase Degrader
(1)
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Carbonic Anhydrase Ligands
(3)
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Carbonic Anhydrase Proteins
(33)
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Carbonic Anhydrase 1 (CA1) Proteins
(1)
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Carbonic Anhydrase 2 (CA-II) Proteins
(3)
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Carbonic Anhydrase 4 (CA IV) Proteins
(3)
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Carbonic Anhydrase 12 (CA-XII) Proteins
(1)
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Carbonic Anhydrase Related Products (382)
Related Products (382)
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Recombinant Proteins (33)
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Carbonic Anhydrase Isoform Comparison
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2-Methoxybenzoic acid-13C6
0 ImagesCat. No.: HY-N1393SSynonyms: NSC 3778-13C6; O-Methylsalicylic acid-13C6; Salicylic acid methyl ether-13C62-Methoxybenzoic acid (NSC 3778; O-Methylsalicylic acid; Salicylic acid methyl ether)-13C6 is the 13C-labeled 2-Methoxybenzoic acid (HY-N1393). 2-Methoxybenzoic acid is a natural compound with potential salicylate-like effect. 2-Methoxybenzoic acid inhibits carbonic anhydrase activity, elevates intraplatelet cyclic guanosine monophosphate level, and suppresses cytosolic phospholipase A2 phosphorylation. 2-Methoxybenzoic acid suppresses platelet reactivity, including decreased spreading, retraction, and aggregation in platelets. 2-Methoxybenzoic acid ameliorates arterial thrombosis in a dose-dependent manner without affecting normal hemostasis in mice. 2-Methoxybenzoic acid can be used for the research of arterial thrombosis. -
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Ethoxzolamide (Standard)
0 ImagesSynonyms: Redupresin (Standard); L-643786 (Standard); PNU-4191 (Standard)Ethoxzolamide (Standard) is the analytical standard of Ethoxzolamide. This product is intended for research and analytical applications. Ethoxzolamide is a carbonic anhydrase inhibitor with Ki of 1 nM. -
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4-Amino-L-phenylalanine hydrochloride
0 ImagesCat. No.: HY-W141810CAS No.: 62040-55-5Synonyms: H-Phe(4-NH2)-OH hydrochloride4-Amino-L-phenylalanine hydrochloride (H-Phe(4-NH2)-OH) is a metabolic intermediate and an α-carbonic anhydrase (TcCA) activator with a Ka value of 0.75 μM. 4-Amino-L-phenylalanine hydrochloride acts through active site cavity entrance binding and a proton shuttle mechanism to enhance the catalytic rate of CO2 hydration. 4-Amino-L-phenylalanine hydrochloride serves as a diamine monomer for bio-based polymer synthesis and is produced in Escherichia coli via the shikimate pathway. 4-Amino-L-phenylalanine hydrochloride constitutes a structural component of haptens used in immunoassay development. 4-Amino-L-phenylalanine hydrochloride is used for the production of Chloramphenicol (HY-B0239) and Pristinamycin I in Streptomyces venezuelae and S. pristinaespiralis, respectively. 4-Amino-L-phenylalanine hydrochloride is used in research related to Trypanosoma cruzi infection. -
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CA12 modulator-1
0 ImagesCat. No.: HY-180864CAS No.: 183892-93-5CA12 modulator-1 is a carbonic anhydrase 12 (CA 12) modulator. -
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Succinylacetone pyrrole
0 ImagesCat. No.: HY-165581CAS No.: 80037-86-1Succinylacetone pyrrole is a potent inhibitor of δ-aminolevulinic acid dehydratase (ALA dehydratase) with a Ki value of 5 μM. Succinylacetone pyrrole blocks the biosynthetic pathway from ALA to porphobilinogen (PBG) and subsequent porphyrins or corrinoids by competitively binding to ALA dehydratase and inhibiting its activity. Succinylacetone pyrrole can be used for studies on vitamin B12 biosynthesis and its regulatory mechanisms. -
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Carbonic anhydrase inhibitor 25
0 ImagesCat. No.: HY-163753Carbonic anhydrase inhibitor 25 (compound 6a) is a potent carbonic anhydrase inhibitor. Carbonic anhydrase inhibitor 25 shows inhibition for hCA I and hCA II receptor. -
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CAI/II-IN-7
0 ImagesCAI/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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- hCAIX/XII-IN-14
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Indan-5-sulphonamide
0 ImagesCat. No.: HY-132155CAS No.: 35203-93-1Synonyms: NSC 91508Indan-5-sulphonamide (Compd 1) is a carbonic anhydrase inhibitor and anticonvulsant agent, with Ki values of 0.039 nM (hCA XII), 6.5 nM (hCA XIV) and 5.1 nM (hCA XIV), respectively. -
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Procodazole (Standard)
0 ImagesSynonyms: Propazol (Standard); 2-Benzimidazolepropionic acid (Standard)DTA (Standard) is the analytical standard of DTA. This product is intended for research and analytical applications. DTA (2,4-Disulfamyl-5-trifluoromethylaniline) is a cyclic AMP phosphodiesterase inhibitor that binds to erythrocyte carbonic anhydrase. -
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Carbonic anhydrase inhibitor 19
0 ImagesCat. No.: HY-162226CAS No.: 3033374-40-9Carbonic anhydrase inhibitor 19 (compound 26a) inhibits the Glaucoma related isoforms hCA II and hCA XII with Kis of 9.4 nM and 6.7 nM, respectively. Carbonic anhydrase inhibitor 19 reveals an intraocular pressure (IOP) lowering effect. -
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Ethoxzolamide-d5
0 ImagesCat. No.: HY-B1480SCAS No.: 3054664-97-7Synonyms: Redupresin-d5; L-643786-d5; PNU-4191-d5Ethoxzolamide-d5 (Redupresin-d5) is deuterium labeled Ethoxzolamide. Ethoxzolamide is a carbonic anhydrase inhibitor with Ki of 1 nM. -
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Dorzolamide-d3 hydrochloride
0 ImagesCat. No.: HY-B0109ASSynonyms: L671152-d3 hydrochloride; MK507-d3 hydrochlorideDorzolamide-d3 hydrochloride is deuterated labeled Dorzolamide hydrochloride (HY-B0109A). Dorzolamide (L671152) hydrochloride is a potent carbonic anhydrase II inhibitor, with IC50 values of 0.18 nM and 600 nM for red blood cell CA-II and CA-I respectively. Dorzolamide possesses anti-tumor activity. -
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CAII/lX-IN-2
0 ImagesCAII/lX-IN-2 is a carbonic anhydrase inhibitor with an IC50 of 2.2 nM against hCA IX and 19.8 nM against hCA XII. CAII/lX-IN-2 inhibits the catalytic activities of cytosolic hCA I, hCA II, and transmembrane tumor-associated hCA IX and hCA XII in a concentration-dependent manner. CAII/lX-IN-2 can be used in research related to metastatic solid tumors. -
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Furagin (Standard)
0 ImagesSynonyms: Furazidine (Standard); Furazidin (Standard)Furagin (Standard) is the analytical standard of Furagin. This product is intended for research and analytical applications. Furagin (Furazidine) is an analogue of Nitrofurantoin (HY-A0090) and has antibacterial activity. Furagin also inhibits human carbonic anhydrases (Kis: 260 and 57 nM for hCA IX and XII, respectively). -
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Tioxolone (Standard)
0 ImagesTioxolone (Standard) is the analytical standard of Tioxolone. This product is intended for research and analytical applications. Tioxolone is an inhibitor for the carbonic anhydrase. Tioxolone exhibits anti-leishmanial, antitumor, and anti-inflammatory activities. Tioxolone can be used in research of acne and psoriasis. -
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Acipimox (Standard)
0 ImagesSynonyms: K-9321 (Standard)Acipimox (Standard) is the analytical standard of Acipimox. This product is intended for research and analytical applications. Acipimox (K-9321), a nicotinic acid analogue, is an antilipolytic compound. Acipimox stimulates leptin releas, inhibits lipolysis and suppresses systemic levels of free fatty acids (FFAs) and improves insulin sensitivity. -
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Methazolamide (Standard)
0 ImagesMethazolamide (Standard) is the analytical standard of Methazolamide. This product is intended for research and analytical applications. Methazolamide (L584601) is a BBB-penetrable and orally active carbonic anhydrase inhibitor, with a Ki of 14 nM for human carbonic anhydrase II. Methazolamide can reduce intraocular pressure and has a neuroprotective effect, being able to inhibit neuronal apoptosis. Methazolamide can be used in the research of ophthalmic diseases such as glaucoma and cerebrovascular diseases such as subarachnoid hemorrhage. -
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Zonisamide (Standard)
0 ImagesSynonyms: AD 810 (Standard); CI 912 (Standard)Zonisamide (Standard) is the analytical standard of Zonisamide. This product is intended for research and analytical applications. Zonisamide (AD 810) is an orally active carbonic anhydrase inhibitor, with Kis of 35.2 and 20.6 nM for hCA II and hCA V, respectively. Zonisamide exerts neuroprotective effects through anti-apoptosis and upregulating MnSOD levels. Zonisamide also increases the expression of Hrd1, thereby improving cardiac function in AAC rats. Zonisamide can be used in studies of seizure, parkinson’s disease and cardiac hypertrophy. -
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CAIX Inhibitor S4 (Standard)
0 ImagesCat. No.: HY-110243RCAS No.: 1330061-67-0CAIX Inhibitor S4 (Standard) is the analytical standard of CAIX Inhibitor S4 (HY-110243). This product is intended for research and analytical applications. CAIX Inhibitor S4 is a potent and selective inhibitor of carbonic anhydrase IX/XII (CA IX/XII), with a Ki of 7 nM and 2 nM, respectively. CAIX Inhibitor S4 also inhibits CA II and CA I (Ki=546 and 5600 nM, respectively). CAIX Inhibitor S4 can inhibit the number of lung metastasis in orthotopic MDA-MB-231 mouse model without affecting primary tumor growth. -
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