| 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 |
| M20001 | Testolactone | Testolactone was originally synthesized as a possible anabolic steroid. The key structural difference from anabolic steroids is the D-cyclolactone rather than the typical cyclopentyl ring. |
| M19437 | Uvariol | Uvariol (21-Hydroxylanosterol) is a natural product that can be isolated from the roots of Piptostigma fugax. |
| M19329 | Kuwanon T | Kuwanon T is an isoprenylated flavonoid compound isolated from the root bark of Morus alba. Kuwanon T shows protective effects on t-BHP-induced oxidative stress with a EC50 of 30.32 μM. |
| M19325 | Roseoside | Roseoside is a compound isolated from the leaves of Elaeocarpus japonicus. |
| M19258 | Pro-xylane | Pro-xylane (Hydroxypropyl tetrahydropyrantriol) is a biologically active C-glycoside in aqueous media, acts as an activator of glycosaminoglycans (GAGs) biosynthesis. Pro-xylane is the first example of 'Green' chemical used in cosmetic. |
| M19246 | Verrucosin | Verrucosin is a compound isolated from Myristica fragrans. |
| M18323 | 12alpha-Hydroxyrotenone | 12alpha-Hydroxyrotenone |
| M18172 | Sodium Guaiazulene Sulfonate | Sodium Guaiazulene Sulfonate |
| M18064 | Cimifugin 4'-O-β-D-glucopyranoside | Cimifugin 4'-O-β-D-glucopyranoside |
| M18044 | Cyclosiversioside F, 16,25-diacetate | Cyclosiversioside F, 16,25-diacetate |
| M18025 | Quercetin 3-O-rutinoside-7-O-glucoside | Quercetin 3-O-rutinoside-7-O-glucoside |
| M17965 | (1E)-3-Methoxy-8,12-epoxygermacra-1,7,10,11-tetraen-6-one | （1E）-3-Methoxy-8,12-epoxygermacra-1,7,10,11-tetraen-6-one |
| M14918 | Glesatinib hydrochloride | Glesatinib hydrochloride (MGCD265 hydrochloride) is an orally active, potent MET/SMO dual inhibitor. |
| M14891 | tBID | tBID is a selective inhibitor of homeodomain-interacting protein kinase 2 (HIPK2) with an IC50 of 0.33 µM. |
| M14890 | Protein kinase inhibitors 1 hydrochloride | Protein kinase inhibitors 1 hydrochloride is a potent HIPK2 inhibitor, with IC50s of 136 and 74 nM for HIPK1 and HIPK2, and a Kd of 9.5 nM for HIPK2. |
| M14888 | EHT 1610 | EHT 1610 is a strong inhibitor of DYRK’s family kinases, with IC50s of 0.36, 0.59 nM for DYRK1A and DYRK1B, respectively. |
| M14798 | TR antagonist 1 | TR antagonist 1 is a high-affinity thyroid hormone receptor (TR) antagonist with IC50s of 36 and 22 nM for TRα and TRβ, respectively. |
| M14794 | XMD-17-51 Trifluoroacetate | XMD-17-51 Trifluoroacetate is a pyrimido-diazepinone compound that is able to modulate protein kinases. |
| M14793 | WJ460 | WJ460 is a potent myoferlin (MYOF) inhibitor, which interacts directly with MYOF and exerts anti-metastatic activity in the nanomolar range in breast cancer cells. |
| M14787 | TRFS-green | TRFS-green is a highly selective off−on fluorescent probe for imaging thioredoxin reductase (TrxR) in living cells. TRFS-green has the maximum absorbance at around 373 nm. |
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