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￥ 0.00 “angiotensin converting enzyme ace”的搜索结果
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Benazepril HCl
Catalog No. A10123 -
ZD 7155 hydrochloride
Catalog No. A19959 AT1 receptor antagonistZD 7155 hydrochloride is an angiotensin II receptor type 1 (AT1 receptor) antagonist. 了解更多 -
Olodanrigan
Catalog No. A21691 AT2R antagonistOlodanrigan (EMA401) is a highly selective, orally active, peripherally restricted angiotensin II type 2 receptor (AT2R) antagonist. 了解更多 -
Apelin agonist 1
Catalog No. A19035 apelin agonistApelin agonist 1 is an oral selective apelin agonist AM-2995, a agonist of the APJ (APLNR, angiotensin receptor like-1) receptor, may be used in the treatment of cardiovascular conditions. 了解更多 -
Azilsartan Medoxomil
Catalog No. A16420 angiotensin II receptor type 1 拮抗剂Azilsartan medoxomil是一种口服给药的1型血管紧张素II受体拮抗剂，IC50为0.62 nM。 了解更多 -
LCZ696 (Valsartan)
Catalog No. A14206 angiotensin receptor-neprilysin 抑制剂LCZ696 (Valsartan)是一种生物利用型双效血管紧张素受体-中性溶血素抑制剂（ARNi），用于治疗高血压和心力衰竭。 了解更多 -
Tasosartan
Catalog No. A10891 -
PD 123319 ditrifluoroacetate
Catalog No. A13201 angiotensin AT2 receptor 拮抗剂PD 123319 ditrifluoroacetate是一种有效的，选择性的非肽血管紧张素AT2受体拮抗剂。大鼠肾上腺组织和大脑的IC50值分别为34和210 nM。 了解更多 -
Fluxapyroxad
Catalog No. A22073 the succinate dehydrogenase (SQR) enzyme inhibitorFluxapyroxad, a broad-spectrum fungicide, is an inhibitor of the succinate dehydrogenase (SQR) enzyme. 了解更多 -
TAS4464 hydrochloride
Catalog No. A21708 NEDD8 activating enzyme inhibitorTAS4464 (hydrochloride) is a highly potent and selective inhibitor of NEDD8 activating enzyme (NAE), with an IC50 of 0.955 nM. 了解更多 -
Vanin-1-IN-1
Catalog No. A19095 Vanin-1 enzyme inhibitorVanin-1-IN-1 is an inhibitor of vanin-1 enzyme which is a cell surface associated, giycosyiphosphatidyS inositol (GPi) anchored protein and plays an important role in metabolism and inflammation. 了解更多 -
PKAkt1/PKBa Human, Inactive enzyme Human Recombinant
Catalog No. AP4564 Protein Kinase Akt1/PKB alpha, Inactive enzyme Human Recombinant 了解更多 -
PKAkt1/PKBa, active enzyme Human Recombinant
Catalog No. AP4563 Protein Kinase Akt1/PKB alpha, Active enzyme Human Recombinant 了解更多 -
Adenosine deaminase
Catalog No. A19330 Adenosine deaminase is an enzyme that catalyzes the irreversible deamination of adenosine and 2'-deoxyadenosine to inosine and 2'-deoxyinosine, respectively. 了解更多 -
Hyaluronidase
Catalog No. A18232 local anesthetic additiveHyaluronidase (Hyaluronate 4-glycanohydrolase; Hyaluronoglucosaminidase) is a naturally occurring enzyme that depolymerizes hyaluronic acid by cleavage of glycosidic bonds and has been used as a local anesthetic additive. 了解更多 -
Cinnamylamine
Catalog No. A20835 Cinnamylamine can be used for the preparation of Tranylcypromine, a drug that acts as a nonselective and irreversible inhibitor of the enzyme monoamine oxidase (MAO), and is used as an antidepressant and anxiolytic agent. 了解更多 -
Conoidin A
Catalog No. A22167 cell permeable inhibitorConoidin A is a cell permeable inhibitor of T. gondii enzyme peroxiredoxin II (TgPrxII). 了解更多 -
UK-371804 HCl
Catalog No. A22379 uPA inhibitorUK-371804 is a potent and selective urokinase-type plasmogen activator (uPA) inhibitor with excellent enzyme potency (Ki=10 nM) and selectivity profile (4000-fold versus tPA and 2700-fold versus plasmin). 了解更多 -
GPNA hydrochloride
Catalog No. A22452 glutamine transporter ASCT2 inhibitorGPNA hydrochloride is a well known substrate of the enzyme γ-glutamyltransferase (GGT). GPNA hydrochloride is a specific glutamine (Gln) transporter ASCT2 inhibitor. 了解更多 -
Soticlestat
Catalog No. A22516 Soticlestat, also known as TAK 935 and OV935, is an inhibitor of the enzyme cholesterol 24-hydroxylase (CH24H). 了解更多 -
Atabecestat
Catalog No. A22605 BACE1 inhibitorAtabecestat (JNJ-54861911) is a potent brain-penetrant and orally active β-site amyloid precursor protein cleaving enzyme 1 (BACE1) inhibitor, achieves robust and high CSF Aβ reduction. 了解更多 -
Methotrexate disodium
Catalog No. A17943 antifolate agentMethotrexate (Amethopterin) disodium, an antimetabolite and antifolate agent, inhibits the enzyme dihydrofolate reductase, thereby preventing the conversion of folic acid into tetrahydrofolate, and inhibiting DNA synthesis. Methotrexate disodium, also an immunosuppressant and antineoplastic agent, is used for the research of rheumatoid arthritis and a number of different cancers (such as acute lymphoblastic leukemia). 了解更多 -
α-Lipoic Acid
Catalog No. A17341 antioxidantα-Lipoic Acid is an antioxidant, which is an essential cofactor of mitochondrial enzyme complexes. α-Lipoic Acid inhibits NF-κB-dependent HIV-1 LTR activation. α-Lipoic Acid induces endoplasmic reticulum (ER) stress-mediated apoptosis in hepatoma cells. 了解更多 -
mPGES1-IN-3
Catalog No. A20454 mPGES-1 inhibitormPGES1-IN-3 (Compound 17d) is a potent and selective microsomal prostaglandin E2 synthase-1 (mPGES-1) inhibitor, which exhibits excellent mPGES-1 enzyme (IC50: 8 nM), cell (A549 IC50: 16.24 nM) and human whole blood potency (IC50: 249.9 nM). 了解更多 -
Revizinone
Catalog No. A20398 PDE inhibitorRevizinone is a novel selective phosphodiesterase (PDE) inhibitor with IC50 values on this enzyme to 0.036 microM. 了解更多 -
Roflumilast Impurity E
Catalog No. A20365 PDE-4 inhibitorRoflumilast Impurity E is the impurity of Roflumilast. Roflumilast(Daliresp) is a drug which acts as a selective and long-acting inhibitor of the enzyme PDE-4 with an IC50 value of 0.8 nM. 了解更多 -
9-Propenyladenine
Catalog No. A20357 9-Propenyladenine is a mutagenic impurity in tenofovir disoproxil fumarate. Tenofovir is an antiretroviral drug known as nucleotide analogue reverse transcriptase inhibitors, which block reverse transcriptase, a crucial virus enzyme in HIV-1 and HBV. 了解更多 -
RR-11a
Catalog No. A19852 -
UbcH5c-IN-1
Catalog No. A19784 UbcH5c inhibitorUbcH5c-IN-1 (compound 6d) is a potent and selective small-molecule inhibitor of Ubiquitin-conjugating enzyme UbcH5c, with a Kd of 283 nM for E2 UbcH5c-IN-1 by covalent binding with Cys85. 了解更多 -
H-Arg-4MβNA
Catalog No. A19686 H-Arg-4MβNA is a substrate for cathepsin H, used for the detection of enzyme activity in gel electrophoresis. 了解更多 -
BMS-816336
Catalog No. A19528 11β-HSD1 inhibitorBMS-816336 is a novel, potent and orally bioavailable inhibitor against human 11β-hydroxysteroid dehydrogenase type 1 (11β-HSD1) enzyme with an IC50 of 3.0 nM. 了解更多
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