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MW 266.09 Da, Purity >99%. Epithelial sodium channel (eNaC) blocker. At higher concentrations, blocks the Na+/H+ exchange pathway. Also blocks transient reception potential cation (TRPC6 and TRPP3) channels.
Alternative names=ACEE, ACES_HUMAN, AHR_HUMAN, ARACHE, Acetylcholinesterase, Ah receptor, Apoptosis related acetylcholinesterase, Aromatic hydrocarbon receptor, Aryl hydrocarbon receptor, Aryl hydrocarbon receptor precursor, BDPLT5, BXR, CAR, CAR BETA, CARA, CD 87, CD87 antigen, Car 1, Cell cycle regulated protein kinase, Class E basic helix-loop-helix protein 76, Constitutive activator of retinoid response, Constitutive active response, Constitutive androstane receptor, EC 3.4.21.73, HD 7, HD 7B, HD 9, HDAC, HDAC 7B, HDAC 9B, HDAC 9FL, HDAC9_HUMAN, HDRP, HGNC:348, Histone deacetylase 4/5 related protein, Histone deacetylase 7, Histone deacetylase 7B, Histone deacetylase 9, Histone deacetylase 9A, Histone deacetylase-related protein, KIAA0744, KPCD1_HUMAN, MB67, MEF2 interacting transcription repressor protein, MEF2-interacting transcription repressor MITR, MGC97144, MITR, MO 3, Monocyte activation antigen Mo3, N-ACHE, NF-E2-related factor 2, NF2L2_HUMAN, NR1I2_HUMAN, NR1I3_HUMAN, NRF2, Nfe2l2, Nuclear factor, Nuclear factor (erythroid derived 2) like 2, Nuclear factor erythroid 2-related factor 2, Nuclear factor erythroid derived 2 like 2, Nuclear receptor subfamily 1 group I member 2, Nuclear receptor subfamily 1 group I member 3, ONR 1, OTTHUMP00000215173, OTTHUMP00000215174, OTTHUMP00000215175, Orphan nuclear receptor MB67, Orphan nuclear receptor NR1I3, Orphan nuclear receptor PAR 1, Orphan nuclear receptor PXR, PAR, PAR q, PKC, PKC MU, PKCM, PKD, PLAU, PLAUR, PLG, PLK, PLK1_HUMAN, PLMN_HUMAN, PRKCM, PRKD 1, PRR, Plasmin, Plasmin heavy chain A, Plasmin light chain B, Plasminogen, Plasminogen activator receptor urokinase, Plasminogen activator urokinase receptor, Polo-like kinase 1, Pregnane X receptor, Protein kinase C mu, Protein kinase C mu type, Protein kinase D, Protein kinase D1, QPD, STPK 13, SXR, Serine/threonine-protein kinase 13, Serine/threonine-protein kinase D1, Serine/threonine-protein kinase PLK1, Steroid and xenobiotic receptor, U-plasminogen activator, UPA receptor, UPAM, UPAR_HUMAN, URK, URKR, Urinary plasminogen activator, Urinary plasminogen activator receptor, Urokinase plasminogen activator, Urokinase plasminogen activator receptor, Urokinase plasminogen activator surface receptor, Urokinase type plasminogen activator, YT, YT blood group, bHLHe76, constitutive active receptor, constitutive androstane nuclear receptor variant 2, constitutive androstane nuclear receptor variant 3, constitutive androstane nuclear receptor variant 4, constitutive androstane nuclear receptor variant 5, erythroid derived 2, like 2, nPKC-D1, nPKC-mu, nuclear factor erythroid 2 like 2, orphan nuclear hormone receptor, pregnane X nuclear receptor variant 2, u plasminogen activator receptor, u-PA, u-plasminogen activator receptor form 2, urokinase-type plasminogen activator (uPA) receptor
2016-88-8
> 99%
Solid
266.09 Da
C6H8ClN7OClH
16230
Synthetic
MW 266.09 Da, Purity >99%. Epithelial sodium channel (eNaC) blocker. At higher concentrations, blocks the Na+/H+ exchange pathway. Also blocks transient reception potential cation (TRPC6 and TRPP3) channels.
Alternative names=ACEE, ACES_HUMAN, AHR_HUMAN, ARACHE, Acetylcholinesterase, Ah receptor, Apoptosis related acetylcholinesterase, Aromatic hydrocarbon receptor, Aryl hydrocarbon receptor, Aryl hydrocarbon receptor precursor, BDPLT5, BXR, CAR, CAR BETA, CARA, CD 87, CD87 antigen, Car 1, Cell cycle regulated protein kinase, Class E basic helix-loop-helix protein 76, Constitutive activator of retinoid response, Constitutive active response, Constitutive androstane receptor, EC 3.4.21.73, HD 7, HD 7B, HD 9, HDAC, HDAC 7B, HDAC 9B, HDAC 9FL, HDAC9_HUMAN, HDRP, HGNC:348, Histone deacetylase 4/5 related protein, Histone deacetylase 7, Histone deacetylase 7B, Histone deacetylase 9, Histone deacetylase 9A, Histone deacetylase-related protein, KIAA0744, KPCD1_HUMAN, MB67, MEF2 interacting transcription repressor protein, MEF2-interacting transcription repressor MITR, MGC97144, MITR, MO 3, Monocyte activation antigen Mo3, N-ACHE, NF-E2-related factor 2, NF2L2_HUMAN, NR1I2_HUMAN, NR1I3_HUMAN, NRF2, Nfe2l2, Nuclear factor, Nuclear factor (erythroid derived 2) like 2, Nuclear factor erythroid 2-related factor 2, Nuclear factor erythroid derived 2 like 2, Nuclear receptor subfamily 1 group I member 2, Nuclear receptor subfamily 1 group I member 3, ONR 1, OTTHUMP00000215173, OTTHUMP00000215174, OTTHUMP00000215175, Orphan nuclear receptor MB67, Orphan nuclear receptor NR1I3, Orphan nuclear receptor PAR 1, Orphan nuclear receptor PXR, PAR, PAR q, PKC, PKC MU, PKCM, PKD, PLAU, PLAUR, PLG, PLK, PLK1_HUMAN, PLMN_HUMAN, PRKCM, PRKD 1, PRR, Plasmin, Plasmin heavy chain A, Plasmin light chain B, Plasminogen, Plasminogen activator receptor urokinase, Plasminogen activator urokinase receptor, Polo-like kinase 1, Pregnane X receptor, Protein kinase C mu, Protein kinase C mu type, Protein kinase D, Protein kinase D1, QPD, STPK 13, SXR, Serine/threonine-protein kinase 13, Serine/threonine-protein kinase D1, Serine/threonine-protein kinase PLK1, Steroid and xenobiotic receptor, U-plasminogen activator, UPA receptor, UPAM, UPAR_HUMAN, URK, URKR, Urinary plasminogen activator, Urinary plasminogen activator receptor, Urokinase plasminogen activator, Urokinase plasminogen activator receptor, Urokinase plasminogen activator surface receptor, Urokinase type plasminogen activator, YT, YT blood group, bHLHe76, constitutive active receptor, constitutive androstane nuclear receptor variant 2, constitutive androstane nuclear receptor variant 3, constitutive androstane nuclear receptor variant 4, constitutive androstane nuclear receptor variant 5, erythroid derived 2, like 2, nPKC-D1, nPKC-mu, nuclear factor erythroid 2 like 2, orphan nuclear hormone receptor, pregnane X nuclear receptor variant 2, u plasminogen activator receptor, u-PA, u-plasminogen activator receptor form 2, urokinase-type plasminogen activator (uPA) receptor
2016-88-8
> 99%
Solid
266.09 Da
C6H8ClN7OClH
16230
Synthetic
Amiloride hydrochloride
Epithelial sodium channel (eNaC) blocker. At higher concentrations, blocks the Na+/H+ exchange pathway. Also blocks transient reception potential cation (TRPC6 and TRPP3) channels.
C1(=C(N=C(C(=N1)Cl)N)N)C(=O)N=C(N)N.Cl
InChI=1S/C6H8ClN7O.ClH/c7-2-4(9)13-3(8)1(12-2)5(15)14-6(10)11;/h(H4,8,9,13)(H4,10,11,14,15);1H
ACHKKGDWZVCSNH-UHFFFAOYSA-N
3,5-diamino-6-chloro-N-(diaminomethylidene)pyrazine-2-carboxamide;hydrochloride
Ambient - Can Ship with Ice
Ambient
The product can be stored for up to 12 months
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