| 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 |
| M7275 | SC 58125 | SC 58125 is a selective cyclooxygenase-2 (COX-2) inhibitor. |
| M7272 | SBHA | SBHA is a histone deacetylase inhibitor. |
| M7270 | SB 772077B dihydrochloride | SB 772077B dihydrochloride is a potent Rho-kinase inhibitor; vasodilator. |
| M7269 | SB 747651A dihydrochloride | SB 747651A dihydrochloride is a potent MSK1 inhibitor; also inhibits other AGC group kinases. |
| M7268 | SB 674042 | SB 674042 is a potent and selective non-peptide OX 1 antagonist. |
| M7266 | SB 611812 | SB 611812 is a urotensin-II (UT) antagonist; attenuates cardiac dysfunction. |
| M7262 | SB 332235 | SB 332235 is a potent CXCR2 antagonist. |
| M7260 | SB 258585 hydrochloride | SB 258585 hydrochloride is a potent, selective 5-HT 6 antagonist. |
| M7257 | SB 222200 | SB 222200 is a potent, selective non-peptide NK 3 antagonist. Brain penetrant. |
| M7256 | SB 221284 | SB 221284 is a potent, selective 5-HT 2C/2B antagonist. |
| M7254 | SB 215505 | SB 215505 is a 5-HT 2B/2C antagonist. |
| M7253 | SB 206553 hydrochloride | SB 206553 hydrochloride is a potent, selective 5-HT 2C/5-HT 2B antagonist. Orally active. |
| M7251 | SB 204741 | SB 204741 is a potent, selective 5-HT 2B antagonist. |
| M7250 | SB 204070 | SB 204070 is a potent and selective 5-HT 4 antagonist. |
| M7247 | SAR7334 dihydrochloride | SAR7334 dihydrochloride is a novel, highly potent and bioavailable inhibitor of TRPC6 channels, inhibiting TRPC6 currents with IC50 of 7.9 nM. |
| M7245 | Salsolinol-1-carboxylic acid | Salsolinol-1-carboxylic acid is a endogenous amino acid. |
| M7243 | SAG 21k | SAG 21k is a hedgehog signaling activator; brain penetrant and orally bioavailable. |
| M7241 | SA 57 | SA 57 is a potent FAAH inhibitor. |
| M7240 | SA 47 | SA 47 is a selective FAAH inhibitor. |
| M7239 | S4 | S4 is a high affinity and selective CA IX and CA XII inhibitor. |
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