New products are an essential component of our range. Introductions are made on an ongoing basis, with hundreds of new small molecules, peptides and antibodies being added every year. Our aim is to find the latest, otherwise unobtainable research tools, and bring them to the market as quickly as we can.
| Cat.No. | Product Name | Activity |
| 5607 | GNF 7 | Ras signaling inhibitor; inhibits Ack1 and GCK |
| 5601 | DMXAA | mSTING agonist; induces antitumor immunological responses |
| 5600 | BA 1 | Potent BRS-3 agonist; also NMBR and GRPR agonist |
| 5594 | Spadin | Potent TREK-1 channel inhibitor |
| 5306 | KJ Pyr 9 | High affinity Myc inhibitor |
| 4831 | NS 3861 | α3β2 full agonist; also α3β4 partial agonist |
| 4829 | ML 239 | Breast cancer stem cell inhibitor |
| 1374 | SB 215505 | 5-HT2B/2C antagonist |
| 5603 | (-)-JQ1 | Inactive control for (+)-JQ1 (Cat. No. 4499) |
| 5576 | PFI 4 | Potent and selective BRPF1 bromodomain inhibitor |
| 5443 | AM 6545 | High affinity and selective CB1 antagonist |
| 5571 | Lei-Dab 7 | Potent, selective KCa2.2 blocker |
| 5554 | IHR 1 | Potent Smo antagonist |
| 5489 | XD 14 | BET bromodomain inhibitor |
| 5485 | GlyH 101 | Reversible, voltage-dependent CFTR chloride channel blocker |
| 5470 | QAQ dichloride | Photoswitchable Nav, Kv and Cav channel blocker |
| 5232 | AZ 191 | Potent DYRK1B inhibitor |
| 5079 | ABT 089 dihydrochloride | High affinity and selective α4β2 partial agonist |
| 4784 | Edaglitazone | Potent and selective PPARγ agonist; antidiabetic |
| 5567 | EPZ 004777 | Highly potent DOT1L inhibitor |
| 5511 | Sucrose | Disaccharide used in biological buffers |
| 5507 | Carbenicillin disodium salt | Antibiotic; selection reagent for AMPR transformed cells |
| 5505 | Kanamycin sulfate | Broad spectrum antibiotic |
| 5498 | AP 811 | High affinity, selective NPR3 antagonist |
| 5484 | C 87 | TNF-α inhibitor |
| 5462 | AAQ chloride | Photoswitchable Kv channel blocker |
| 5456 | Zosuquidar trihydrochloride | High affinity P-gp inhibitor |
| 5379 | VU 0469650 hydrochloride | Potent and selective negative allosteric modulator of mGlu1 |
| 5378 | VU 0422288 | Selective group III mGlu positive allosteric modulator |
| 5368 | Maritoclax | Mcl-1 inhibitor; proapoptotic |
| 5246 | MRS 1477 | TRPV1 positive allosteric modulator |
| 5185 | JTE 607 dihydrochloride | Cytokine release inhibitor; anti-inflammatory |
| 5129 | TC-G 1005 | Potent and selective TGR5 agonist |
| 5124 | PD 404182 | High affinity inhibitor of KDO 8-P synthase; also DDAH1 inhibitor |
| 4860 | ML 193 | Potent, selective GPR55 antagonist |
| 4702 | ETP 45658 | Potent PI 3-kinase inhibitor; also inhibits DNA-PK and mTOR |
| 4597 | NS 8593 hydrochloride | Selective KCa2 (SK) channel negative modulator; inhibits SK currents |
| 4492 | Cerestat | Potent and noncompetitive NMDA receptor antagonist |
| 4482 | PR 619 | Broad spectrum DUB inhibitor |
| 3105 | FK 409 | NO donor |