Non-Antibody Products — page 1 of 406
Non-Antibody Products
Page 1 of 406
| Name | Description | Size | Catalog # | Supplier | |
|---|---|---|---|---|---|
| 666-15 | 666-15 is a potent and selective inhibitor of CREB-mediated gene transcrip… | n/a | 1433286-70-4 |
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| 360A | 360A is a strong affinity and selectivity inhibitor of G-quadruplex struct… | n/a | 794458-56-3 |
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| A 1070722 | A 1070722 is a potent glycogen synthase kinase-3 (GSK-3) inhibitor (Ki = 0… | n/a | 1384424-80-9 |
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| A 1120 | A 1120 is a retinol-binding protein 4 (RBP4) antagonist (Ki = 8.3 nM) that… | n/a | 1152782-19-8 |
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| A 127722 | A 127722 is a potent and selective ETA endothelin receptor antagonist (IC5… | n/a | 195704-72-4 |
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| A 196 | A 196 is a potent and selective inhibitor of SUV420H1 / H2 (IC50 = 25 and… | n/a | 1982372-88-2 |
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| A 286982 | A 286982 is a potent inhibitor of the LFA-1 / ICAM-1 interaction (IC50 = 4… | n/a | 280749-17-9 |
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| A 33 | A 33 is a potent and selective PDE4B inhibitor (IC50 = 15 nM) that exhibit… | n/a | 915082-52-9 |
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| A 410099.1 | A 410099.1 is a high affinity XIAP antagonist (Kd = 16 nM for the BIR3 dom… | n/a | 762274-58-8 |
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| A 419259 | A-419259 is a potent inhibitor of Src family kinases. IC50 values for src,… | n/a | 364042-47-7 |
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| A 425619 | A 425619 is a potent and selective TRPV1 antagonist (IC50 = 3-9 nM) that i… | n/a | 581809-67-8 |
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| A 437203 | Purity >98%. MW: 456.53. Molecular Formula: C20H27F3N6OS | n/a | 220519-06-2 |
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| A 484954 | A 484954 is a eukaryotic elongation factor-2 (eEF-2) kinase inhibitor (IC5… | n/a | 142557-61-7 |
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| A 582941 | A 582941 is a selective α7 nAChR partial agonist which is effetive f… | n/a | 848591-90-2 |
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| A 71915 | A 71915 is a highly potent and competitive natriuretic peptide receptor A… | n/a | 132956-87-7 |
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| A 779 | A 779 is a specific antagonist of G-protein coupled receptor (Mas receptor… | n/a | BAT-006218 |
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| A 784168 | A 784168 is a potent and selective TRPV1 antagonist (IC50 = 25 nM for inhi… | n/a | 824982-41-4 |
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| A 804598 | A 804598 is a potent and competitive P2X7 receptor antagonist (IC50 = 8.9,… | n/a | 1125758-85-1 |
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| A 839977 | A-839977 is a novel and selective P2X7 antagonist. It blocks BzATP-evoked… | n/a | 870061-27-1 |
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| A 841720 | A 841720 is a potent non-competitive mGlu1 receptor antagonist (IC50 = 10… | n/a | 869802-58-4 |
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| A 844606 | A 844606 is a selective α7 nicotinic acetylcholine receptor (nAChR)… | n/a | 861119-08-6 |
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| A 887826 | A 887826 is a potent voltage-dependent NaV1.8 channel blocker (IC50 = 11 n… | n/a | 1266212-81-0 |
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| A 943931 | A 943931 is a potent and selective histamine H4 receptor antagonist. Purit… | n/a | 1027330-97-7 |
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| A 967079 | A 967079 is a selective TRPA1 channel blocker (IC50 = 67 and 289 nM at hum… | 100mg | B0084-359603 |
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| A 987306 | A 987306 is a potent histamine H4 receptor antagonist (pKi = 8.24 and 8.47… | n/a | 1082954-71-9 |
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| A01 | A01 is a high affinity Smurf1 E3 ubiquitin ligase inhibitor (Kd = 3.7 nM),… | n/a | 1007647-73-5 |
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| A-1155463 | A-1155463, an effective and selective BCL-XL inhibitor, has been studied t… | n/a | B0084-474415 |
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| A-1165442 | A-1165442 is a potent, competitive and orally available modality-different… | n/a | 1221443-94-2 |
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| A-1210477 | A-1210477 is a potent and selective MCL-1 inhibitor with Ki and IC50 of 0.… | n/a | 1668553-26-1 |
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| A-1331852 | A-1331852, a substituted benzothiazole, is a high affinity BH3 mimetic Lig… | 100mg | B0084-007703 |
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| A-192621 | A-192621 is a selective antagonist at endothelin ETB receptor with more ef… | n/a | 195529-54-5 |
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| A-205804 | A-205804 is a potent and selective inhibitor of E-selectin and ICAM-1 expr… | n/a | 251992-66-2 |
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| A-366 | A-366 is peptide-competitive inhibitor of the G9a / GLP histone lysine met… | n/a | 1527503-11-2 |
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| A-366833 | A-366833 is a an agonist at neural nicotinic acetylcholine receptors selec… | n/a | 370882-41-0 |
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| A-443654 | A-443654 is a potent small-molecule inhibitor of all three Akt serine / th… | n/a | 552325-16-3 |
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| A-485 | A-485 is an inhibitor of the histone acetyltransferase p300 / CBP (IC50 =… | n/a | 1889279-16-6 |
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| A66 | Inhibition of p110α alone by A66 treatment is sufficient to block in… | n/a | 1166227-08-2 |
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| A-674563 | A-674563 is an Akt1 inhibitor with Ki of 11 nM, modest potent to PKA and >… | 10mg | B0084-307687 |
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| A-71623 | A-71623 is a tetrapeptide and acts as a potent CCK1 agonist (IC50 = 3.7 nM… | n/a | 130408-77-4 |
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| A-740003 | A-740003 is potent, selective and competitive P2X7 receptor antagonist. It… | n/a | 861393-28-4 |
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| A-769662 | A-769662 is a potent, reversible AMPK activator with EC50 of 0.8 µM… | n/a | 844499-71-4 |
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| A-770041 | A-770041 is an selective and orally bioavailable pyrazolo[3,4-d]pyrimidine… | n/a | 869748-10-7 |
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| A-77-01 | A-77-01 is an inhibitor of TGF-β type I receptor superfamily activin-… | n/a | 607737-87-1 |
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| A-802715 | A802715, a methylxanthine derivative, is an anti-tumor agent with a TD50 (… | n/a | 107767-58-8 |
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| A-803467 | A-803467 is a sodium channel blocker that potently blocks tetrodotoxin-res… | n/a | 944261-79-4 |
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| A81988 | A81988 is a potent, orally active angiotensin I1 antagonist with a long du… | n/a | 141887-34-5 |
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| A-83-01 | A 83-01 is an inhibitor of TGF-β type I receptor kinase (ALK5), activ… | 50mg | B0084-155117 |
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| A-836339 | A-836339 is a synthetic and potent cannabinoid receptor full agonist. It d… | n/a | 959746-77-1 |
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| A-867744 | A-867744 is a positive allosteric modulator of α7 nAChRs (IC50 value… | n/a | 1000279-69-5 |
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| A-893 | A-893 is an inhibitor of SMYD2, which is a lysine methyltransferase. The c… | n/a | 1868232-32-9 |
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