| Cat.No. | Name | Information |
|---|---|---|
| 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 |
| M7791 | Exo-1 | Exo1 is a reversible inhibitor of exocytosis, also a Golgi ARF 1 (ADP-Ribosylation Factor) GTPase activator. |
| M4321 | Gelsemine | Gelsemine is an alkaloid derived from the Chinese herb Gelsemium Elegans, which is effective in relieving chronic pain. Gelsemine has anti-injury and sleep-promoting effects. |
| M4319 | 23S-hydroxyl-11,15-dioxo-ganoderic-acid-DM | 23S-hydroxyl-11,15-dioxo-ganoderic-acid-DM |
| M4318 | Lucidenic-acid-D | Lucidenic acid D (Lucidenic acid D2) is a highly oxidized lanosterane triterpenoid. |
| M4317 | Ganoderenic-acid-E | Ganoderenic acid E is a triterpenoid compound. |
| M4316 | Deacetyl-ganoderic-acid-F | Deacetyl Ganoderic Acid F is a triterpenoid derived from Ganoderma Lucidum. |
| M4312 | Lucidenic-acid-E | Lucidenic acid E is a terpene derived from ganoderma lucidum. |
| M4309 | Ganoderic-acid-G | Ganoderic acid G is a triterpenoid compound isolated from the tube surface of Ganoderma lucidum. |
| M4308 | Ganoderic-acid-F | Ganoderic acid E is a triterpenoid compound found in ganoderma lucidum. |
| M4303 | Khasianine | Khasianine is a steroid sugar alkaloid. It is a natural product extracted from Solanum Nigrum L, a solanum plant, and has strong activity against CCl4 induced liver injury. It has anti-tumor activity. |
| M4297 | Tenacissoside-I | Tenacissoside I is a C21 steroid from Marsdenia tenacissima, with high concentrations in M. tenacissima. |
| M4296 | Tenacissoside-H | Tenacissoside H is a natural product isolated from Tenacissoside H, which has anti-tumor effect. |
| M4292 | Magnoflorine | Magnoflorine |
| M4291 | Atractylodin | Atractylodin (Atractydin) is the active ingredient of essential oils contained in the rhizome of Atractylodes lancea and A. chinensis. Atractylodin is a natural insecticide that is resistant to Tribolium Castaneum. |
| M4286 | Angoroside-C | Angoroside C is a phenylalanine extracted from Radix Scrophulariae, which is beneficial for ventricular remodeling. |
| M4273 | Sipeimine | Sipeimine is a natural product isolated from fritillaria fritillaria. |
| M4267 | Hupehenine | Hupehenine is a bioactive isosteroidal alkaloid that is the main cough suppressant in Fritillariae Bulbus. |
| M4266 | Hapepunine | Hapepunine |
| M4260 | Chamigrenal | Chamigrenal isa natural product and can be obtained from Schisandra sphenanthera fruit. |
| M4258 | Gomisin-D | Gomisin D isa lignan compound isolated from Fructus Schisandra (Fructus Schisandra) that isa potential antidiabetic and anti-Alzheimer's drug. Gomisin D inhibits UDP-glucuronyl transferase activity and scavenge ABTS(+) free radicals. Gomisin D is used as a quality marker of Shengmai SAN and Shenqi Jiangtang granules. |
| M4251 | Schisanhenol | Schisanhenol is a natural compound that has been reported as an inhibitor of UGT2B7. |
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