| Cat.No. | Name | Information |
|---|---|---|
| M2206 | TH-302 (Evofosfamide) | TH-302 is a highly potent and selective hypoxia-activated procompound targeting hypoxic regions of solid tumors with IC50 of 19 nM. |
| M6098 | Baicalein | Baicalein is a CYP2C9 and prolyl endopeptidase inhibitor, IC50 value of 3.12 mM. |
| M9325 | EGTA | EGTA is a specific calcium chelator with a Kd of 60.5 nM at physiological pH (7.4) and a high specificity for Ca2+ than for Mg2+.EGTA significantly inhibits the substrate adhesion capacity of inflammatory macrophages. |
| M9330 | Brij-35 | Brij-35 (Polidocanol) is a high HLB, ethoxylated, nonionic ether of lauryl alcohol with broad pH stability. |
| M6154 | 2-PMPA tetrasodium | 2-PMPA (PMPA tetrasodium salt) is a potent and selective inhibitor of glutamate carboxypeptidase II (GCPII) with an IC50 of 300 pM. |
| M2250 | Pamidronate disodium | Pamidronate disodium is a nitrogen containing bisphosphonate, used to the research of preventing osteoporosis. |
| M9916 | DPPH | DPPH (2,2-Diphenyl-1-picrylhydrazyl) is a stable free radical that measures the free radical scavenging activity of antioxidants. |
| M9194 | Insulin (human) | Insulin (human) is a polypeptide hormone that regulates the level of sugar (glucose) in the blood and is produced by beta cells of islets. |
| M3409 | Formestane | Formestane is a second generation selective aromatase inhibitor with an IC50 of 80 nM. |
| M9665 | N-(2-amino-2-oxoethyl)acrylamide | N-(2-Amino-2-oxoethyl)acrylamide |
| M43022 | ZIKV-IN-6 | ZIKV-IN-6 is an inhibitor of Zika virus (ZIKV), with low cytotoxicity (CC50＞50 μM). |
| M43021 | CRT0063465 | CRT0063465 is a Ligand of HumanPGK1andStress Sensor DJ1, with theKdof 24 μM ofPGK1. |
| M43020 | NH2-UAMC1110 | NH2-UAMC1110 is a UAMC1110 derivative that can be used in the synthesis of FAPI-QS. |
| M43018 | TAS2R14 agonist-1 | TAS2R14 agonist is a potent TAS2R14 partial agonist with an EC50 of 116.6 ±23.6 nM. |
| M43017 | Wnt pathway inhibitor 4 | Wnt pathway inhibitor 4 is an anticancer agent that has anti-proliferative activity. |
| M43016 | Activated EG3 Tail | Activated EG3 Tail can be used in the synthesis of exon jumping oligomer conjugates. |
| M43015 | Sunepitron hydrochloride | Sunepitron (CP-93,393) hydrochloride is a potent anxiolytic/antidepressantcan agent. |
| M43014 | TIBI | TIBI is a potent and ATP-competitive inhibitor of Rio1 (IC50: 0.09 μM, Ki: 0.05 μM). |
| M43012 | Progranulin modulator-1 | Progranulin modulator-1 is an orally active enhancer of progranulin (PGRN) secretion. |
| M43011 | PI5P4Ks-IN-2 | PI5P4Ks-IN-2 is a inhibitor of phosphatidylinositol 5-phosphate 4-kinase γ (PI5P4Kγ). |
| M43010 | Activated T Subunit | Activated T Subunit can be used in the synthesis of exon jumping oligomer conjugates. |
| M43009 | Activated C Subunit | Activated C Subunit can be used in the synthesis of exon jumping oligomer conjugates. |
| M43008 | Activated A Subunit | Activated A Subunit can be used in the synthesis of exon jumping oligomer conjugates. |
| M43007 | Sinomenine N-oxide | Sinomenine N-oxide has anti-angiogenic, anti-inflammatory and anti-rheumatic effects. |
| M43006 | DIOA | DIOA is a potent acid-sensitive outwardly rectifying (ASOR) anion channel antagonist. |
| M43005 | LANA-DNA-IN-2 | LANA-DNA-IN-2 is a latency-associated nuclear antigen (LANA)-DNA interaction inhibitor. |
| M43004 | Cisplatin-resistant cells-IN-1 | Cisplatin-resistant cells-IN-1 has high cytotoxicity against Cisplatin-resistant cells. |
| M43003 | BTTES | BTTES is a tris(triazolylmethyl)amine-based ligand for Cu(I) without apparent toxicity. |
| M43002 | Activated DPG Subunit | Activated DPG Subunit can be used in the synthesis of exon jumping oligomer conjugates. |
| M43001 | MI-1481 | MI-1481 is a highly potent inhibitor of the Menin-MLL1 interaction with IC50 of 3.6 nM. |
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