| 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 |
| 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. |
| M7238 | S 32826 | S 32826 is a potent autotaxin inhibitor. |
| M7236 | S 18986 | S 18986 is a positive allosteric modulator of AMPA. |
| M7235 | Ryuvidine | Ryuvidine is a sETD8 inhibitor; also CDK4 inhibitor. |
| M7233 | RWJ 52353 | RWJ 52353 is a α 2D agonist. |
| M7232 | RWJ 50271 | RWJ 50271 is a inhibitor of LFA-1/ICAM mediated cell adhesion. |
| M7231 | RWJ 21757 | RWJ 21757 is a toll-like receptor 7 (TLR7) agonist. |
| M7230 | RuBi-4AP | RuBi-4AP is a caged 4-aminopyridine; a non-selective K V channel blocker. |
| M7229 | RU 58668 | RU 58668 is a pure antiestrogen. |
| M7228 | RU 28318, potassium salt | RU 28318, potassium salt is a potent, selective mineralocorticoid receptor antagonist. |
| M7225 | RS 56812 hydrochloride | RS 56812 hydrochloride is a 5-HT 3 partial agonist. |
| M7223 | RS 45041-190 hydrochloride | RS 45041-190 hydrochloride is a high affinity I 2 ligand. Highly selective. |
| M7222 | RS 25344 hydrochloride | RS 25344 hydrochloride is a potent PDE4 inhibitor. |
| M7221 | RS 23597-190 hydrochloride | RS 23597-190 hydrochloride is a 5-HT 4 antagonist. |
| M7220 | RS 17053 hydrochloride | RS 17053 hydrochloride is a α 1A antagonist. |
| M7219 | RS 127445 hydrochloride | RS 127445 hydrochloride is a selective, high affinity 5-HT 2B antagonist. |
| M7217 | RS 100329 hydrochloride | RS 100329 hydrochloride is a potent, subtype-selective α 1A antagonist. |
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