| 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 |
| M43050 | N-Acetylsulfanilamide | N-Acetylsulfanilamide is a compound with potential anti-infective activity. |
| M43049 | BLK degrader 1 | BLK degrader 1 is a selective degrader of B-lymphoid tyrosine kinase (BLK). |
| M43048 | E235 | E235 is an expression regulator of activates transcription factor 4 (ATF4). |
| M43047 | PRDX1-IN-1 | PRDX1-IN-1 is a selective inhibtor of PRDX1 with an IC50 value of 0.164 μM. |
| M43046 | RASP-IN-1 | RASP-IN-1 is a lipophili ccompound used for macular degeneration inhibition. |
| M43045 | Tibric acid | Tibric acid (CP 18524) has similar effects to those of hypolipidemic agents. |
| M43044 | 21-Desacetyldeflazacort | 21-Desacetyldeflazacort (21-desDFZ) is the active metabolite of Deflazacort. |
| M43043 | Clibucaine | Clibucaine is a piperidine derivative possessing local anesthetic properties. |
| M43042 | IA1-8H2 | IA1-8H2 is a non-covalent, non-competitive inhibitor of PHPT1 (IC50: 3.4 μM). |
| M43041 | NCP2 Anchor | NCP2 Anchor can be used in the synthesis of exon jumping oligomer conjugates. |
| M43040 | PI5P4K-β-IN-2 | PI5P4K-β-IN-2 is a PI5P4K-β inhibitor (IC50=0.35 μM) with antitumor activity. |
| M43039 | Tixocortol pivalate | Tixocortol pivalate is a corticosteroid with some anti-inflammatory activity. |
| M43038 | Steroid sulfatase-IN-5 | Steroid sulfatase-IN-5 is a steroid sulfatase (STS) inhibitor (IC50: 0.32 nM). |
| M43037 | Immune cell migration-IN-1 | Immune cell migration-IN-1 is a potent agent to inhibit immune cell migration. |
| M43036 | PPO-IN-2 | PPO-IN-2 is an inhibitor of protoporphyrinogen IX oxidase with an Ki of 16 nM. |
| M43035 | Rocbrutinib | Rocbrutinib is a Bruton's tyrosine kinase inhibitor with antineoplastic effect. |
| M43034 | Steroid sulfatase-IN-6 | Steroid sulfatase-IN-6 is an irreversible inhibitor of steroid sulfatase (STS). |
| M43033 | PI5P4Kα-IN-1 | PI5P4Kα-IN-1 is a PI5P4Kinhibitor (IC50: 2 and 9.4 μM for PI5P4Kα and PI5P4Kβ). |
| M43032 | TNG-0746132 | TNG-0746132 can be used for synthesis of the compound with anticancer activity. |
| M43031 | Hi 76-0079 | Hi 76-0079 is a hormone-sensitive lipase (HSL) inhibitor with an IC50 of 184 nM. |
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