Non-Antibody Products — page 1 of 203
Non-Antibody Products
Page 1 of 203
| 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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| A-92 | A-92 inhibits the stress response of general control nonderepressible 2 ki… | n/a | 1448693-69-3 |
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| A922500 | A922500 is an inhibitor for human and mouse DGAT-1 with IC50 of 7 nM and 2… | n/a | 959122-11-3 |
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| A-966492 | A-966492 is a novel and potent inhibitor of PARP1 and PARP2 with Ki of 1 n… | n/a | 934162-61-5 |
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| AA 147 | AA 147 is an endoplasmic reticulum (ER) proteostasis regulator. Activates… | n/a | 393121-74-9 |
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| AA 29504 | AA 29504 is a positive allosteric modulator of GABAA receptors with anxiol… | n/a | 945828-50-2 |
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| AA26-9 | AA26-9, synthesized based on a piperazine scaffold, is a potent and broad… | n/a | 1312782-34-5 |
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| AACOCF | AACOCF, an anlogue of arachidonic acid, is a slow-binding inhibitor of cyt… | n/a | 149301-79-1 |
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| AAE871 | Purity >98%. MW: 498.64. Molecular Formula: C24H34N8O2S | n/a | 289479-07-8 |
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| AAF-CMK trifluoroacetate salt | AAF-CMK trifluoroacetate salt is a serine peptidase of the subtilisin-type… | n/a | 184901-82-4 |
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| 17-AAG hydrochloride | 17-AAG hydrochloride is a potent HSP90 inhibitor with IC50 value of 5 nM,… | n/a | 911710-03-7 |
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| AAI101 | AAI101 is a novel β-lactamase inhibitor with activity against extende… | n/a | 1001404-83-6 |
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| AAL-993 | Purity >98%. MW: 371.363. Molecular Formula: C20H16F3N3O | n/a | 269390-77-4 |
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| Aaptamine | Aaptamine, a spongean alkaloid isolated from a sea sponge Aaptos aaptos, i… | n/a | 85547-22-4 |
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| A2AR-agonist-1 | A2AR-agonist-1 is a potent A2AR (Ki = 4.39) and ENT1(Ki = 3.47 ) agonist.… | n/a | 41552-95-8 |
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| A2AR antagonist 1 | A2AR antagonist 1 is a potent A2AR (Adenosine A2A Receptor) antagonist wit… | n/a | 443103-97-7 |
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| AAT-008 | AAT-008 is an orally bioavailable and potent antagonist of the prostagland… | n/a | 847727-81-5 |
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| A-54556B | A-54556B is a natural acyldepsipeptide (ADEP) antibiotic isolated from the… | n/a | 1629166-56-8 |
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| AB05831 | An analogue of deoxynojirimycin, was found to be a potent inhibitor of a n… | n/a | 105265-96-1 |
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| AB-423 | AB-423 is an inhibitor of HBV capsid assembly, and potent inhibits HBV rep… | n/a | 1572510-80-5 |
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| 8-ABA-cAMP | 8-ABA-cAMP is a selective cAMP analogue oreferring site B of R I of cAMP-d… | n/a | 82927-68-2 |
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| Abacavir | Abacavir sulfate is a Nucleoside analog reverse transcriptase inhibitor (N… | n/a | 136470-78-5 |
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| Abacavir 5?-4-Chloro-6-methylpyrimidine-2,5-diamine | Abacavir 5?-4-Chloro-6-methylpyrimidine-2,5-diamine (Abacavir EP Impurity… | n/a | 1443421-69-9 |
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| Abacavir Sulfate | Abacavir is a commonly used nucleoside analogue with potent antiviral acti… | n/a | 188062-50-2 |
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| Abacavir sulfate | Abacavir is an antiviral analog of guanosine, inhibiting the reverse trans… | n/a | 216699-07-9 |
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| Abacavir 5?-(2,3,4-Tri-O-isobytyryl)-β-D-glucuronic Acid Methyl Ester | Abacavir 5?-(2,3,4-Tri-O-isobytyryl)-β-D-glucuronic Acid Methyl Ester… | n/a | 38734 |
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| abafungin | Abafungin is a broad-spectrum antifungal agent with a novel mechanism of a… | n/a | 129639-79-8 |
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| Abaloparatide | Abaloparatide is an analogue of parathyroid hormone-related protein (PTHrP… | n/a | BAT-006119 |
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| Abamectin | Avermectin B1 (Abamectin) is a widely used insecticide and anthelmintic. I… | 10g | B0084-097508 |
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| Abanoquil mesilate | This molecular is an active biochemical as a Alpha 1 adrenergic receptor a… | n/a | 118931-00-3 |
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| Abarelix | Abarelix is a synthetic decapeptide and antagonist of naturally occurring… | n/a | BAT-006166 |
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| ABBV-744 | ABBV-744 is a BDII-selective BET bromodomain inhibitor that inhibits BRD2,… | n/a | 2138861-99-9 |
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| A12B4C3 | A12B4C3 is a potent and selective inhibitor of polynucleotide kinase / pho… | n/a | 1005129-80-5 |
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| ABC-1183 | ABC-1183 is an inhibitor of glycogen synthase kinase 3 (GSK-3) alpha, glyc… | n/a | 1042735-18-1 |
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| ABC294640 | ABC294640 is an orally available, aryladamantane compound and selective in… | n/a | 915385-81-8 |
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| ABC294735 | ABC294735 is a dual SK1 / SK2 inhibitor with potential anticancer activity… | n/a | 917236-13-6 |
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| ABC34 | ABC34 is an inactive control probe for JJH260 , the inhibitor of androgen-… | n/a | 1831135-56-8 |
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| ABD459 | ABD459 is a neutral antagonist of the central cannabinoid 1 (CB1) receptor… | n/a | 1047670-51-8 |
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| abemaciclib mesylate | Abemaciclib mesylate is a CDK inhiibitor with selectivity for CDK4 and CDK… | n/a | 1231930-82-7 |
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| ABET | Arecaidine But-2-ynyl Ester Tosylate (ABET) is a potent and selective agon… | n/a | 119630-77-2 |
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| Abexinostat | Abexinostat, also known as PCI-24781 or CRA-024781, is novel, broad-spectr… | 100mg | 783355-60-2 |
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| ABH | ABH is an inhibitor of arginase types I and II. Purity ≥90%. MW: 175. M… | n/a | 222638-65-5 |
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| Abiraterone | Abiraterone blocks the synthesis of androgens by inhibiting CYP17A1. It is… | 5g | B0084-059670 |
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| Abiraterone Acetate | The acetate form of abiraterone, which blocks the synthesis of androgens b… | 10g | B0084-461965 |
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| 3a-Bis-(4-fluorophenyl) methoxytropane hydrochloride | A potent inhibitor of dopamine uptake and transport (Ki = 11.8 nM). MW: 37… | n/a | 202646-03-5 |
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| AbK | AbK is an unnatural amino acid and is genetically encoded for site-selecti… | n/a | 1253643-88-7 |
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| ABL 127 | ABL 127 is a covalent aza-β-lactam inhibitor of protein phosphatase m… | n/a | 1073529-41-5 |
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| AB-MECA | AB-MECA, a adenosine derivative, is a high affinity human A3 receptor in H… | n/a | 152918-26-8 |
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| Abn-CBD | Abn-CBD is a neurobehaviorally inactive cannabinoid and acts as a selectiv… | n/a | 22972-55-0 |
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| ABP 688 | ABP 688 is a high affinity human mGlu5 receptor antagonist (Ki = 1.7 nM) t… | n/a | 924298-51-1 |
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| A2B receptor antagonist 1 | A potent antagonist of A2B adenosine receptor. MW: 392.45. Molecular Formu… | n/a | 531506-36-2 |
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