| 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 prevent 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 |
| M6409 | AF-DX 384 | AF-DX 384 is a potent M 2/M 4 antagonist. |
| M6408 | AEG 3482 | AEG 3482 is a inhibitor of JNK signaling. |
| M6405 | ACT 335827 | ACT 335827 is a potent and selective OX 1 antagonist. |
| M6403 | ACPT-II | ACPT-II is a competitive mGlu receptor antagonist. |
| M6401 | Acifran | Acifran is a hypolipidemic agent; agonist for the GPR109A (HM74A) and GPR109B receptors. |
| M6400 | ACET | ACET is a potent antagonist of GluR5-containing kainate receptors. |
| M6398 | ACDPP hydrochloride | ACDPP hydrochloride is a selective mGlu 5 receptor antagonist. |
| M6397 | ACBC | ACBC is a nMDA antagonist, acts at glycine site. |
| M6391 | AC 261066 | AC 261066 is a rARβ2 agonist. |
| M6390 | ABT 724 trihydrochloride | ABT 724 trihydrochloride is a potent, selective D 4 partial agonist; proerectile. |
| M6388 | ABP 688 | ABP 688 is a high affinity human mGlu 5 receptor antagonist. |
| M6387 | Abn-CBD | Abn-CBD is a selective GPR55 agonist; neurobehaviorally inactive. |
| M6386 | AbK | AbK is a photo-crosslinking probe. |
| M6385 | AA 29504 | AA 29504 is a positive allosteric modulator of GABA A receptors. |
| M6383 | A12B4C3 | A12B4C3 is a potent and selective polynucleotide kinase/phosphatase (PNKP) inhibitor. |
| M6381 | A 987306 | A 987306 is a potent and selective H 4 receptor antagonist. |
| M6377 | A 85380 dihydrochloride | A 85380 dihydrochloride is a high affinity and selective α4β2 agonist. |
| M6354 | 7-Chlorokynurenic acid | 7-Chlorokynurenic acid is a potent competitive inhibitor of L-glutamate uptake. |
| M6320 | 18A | 18A is a hIV cell entry blocker. |
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