| 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 |
| M43000 | TPPC | TPPC, a porphyrin cholesterol conjugate, can render cancer cells more sensitive to ICIs. |
| M42999 | Ac-PLVE-FMK | Ac-PLVE-FMK (Ac-Pro-Leu-Val-Glu(OMe)-CH2F), a tetrapeptidyl m-FMKs, is a Cats inhibitor. |
| M42998 | GBT1118 | GBT1118 is a potent and orally active allosteric modifier of hemoglobin oxygen affinity. |
| M42997 | NVOC cage-TMP-Halo | NVOC cage-TMP-Halo is a cell-permeable and photoactivatable protein dimerization inducer. |
| M42996 | TNH | TNH is a dimer that can enter living cells and recruit proteins into cellular structures. |
| M42995 | RPE65-IN-1 | RPE65-IN-1is a potent RPE65 inhibitor, which can be used in retinopathy-related research. |
| M42994 | 6-Thioinosine Phosphate | 6-Thioinosine Phosphate (Thioinosinic acid) is an intermediate metabolite of azathioprine. |
| M42993 | DAO-IN-1 | DAO-IN-1 is a potent inhibitor of D-amino acid oxidase (DAO) with an IC50 value of 269 nM. |
| M42992 | TAS2R14 agonist-2 | TAS2R14 agonist-2 is a potent and selective TAS2R14 inhibitor with an EC50 value of 72 nM. |
| M42991 | NCGC00138783 TFA | NCGC00138783 TFA is a selective inhibitor targeting CD47/SIRPα axis, with an IC50 of 50 μM. |
| M42990 | Civorebrutinib | Civorebrutinib (WS-413) is a Bruton's tyrosine kinase inhibitor with antineoplastic effect. |
| M42989 | D-Leucinol | D-Leucinol is the inactive isomer of L-Leucinol, and can be used as an experimental control. |
| M42988 | LK-44 | hCES2A-IN-2 is an orally active human carboxylesterase 2 (hCES2A) inhibitor (IC50: 5.02 μM). |
| M42986 | IZS-M | IZS-M is an amino acid-derived corrosion inhibitor, based on the green chemistry principles. |
| M42985 | IZS-P | IZS-P is an amino acid-derived corrosion inhibitor, based on the green chemistry principles. |
| M42984 | SYNTi | SYNTi is a PDZ domain inhibitor targeting the syndecan/syntenin protein-protein Interaction. |
| M42983 | Mofebutazone | Mofebutazone, a monophenyl analogue of Phenylbutazone (DPB), is an anti-inflammatory compound. |
| M42982 | Vamagloxistat | Vamagloxistat is glycolate oxidase inhibitor, used to inhibit hyperoxaluria and kidney stones. |
| M42981 | MSN8C | MSN8C, an analog of mansonone E, is a novel catalytic inhibitor of human DNA topoisomerase II. |
| M42980 | LJP 1586 | LJP 1586 is an amine-based inhibitor of semicarbazide-sensitive amine oxidase (SSAO) activity. |
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