|Description||Ipfencarbazone is a non-hormonal translocation-type herbicide. It is thought to inhibit the biosynthesis of very long chain fatty acids in plants. Preparations include water-dispersible agents and compound fertilizers, and application has been made for these to be used on rice plants.|
Azathioprine is an immunosuppressive drug, inhibiting purine synthesis and GTP-binding protein Rac1 activation, used in the treatment of organ transplantation a...
Albiflorin is a major constituent presents in peony root, which possesses therapeutic potential for neurodegenerative diseases.
GRGDSPK, a linear integrin binding peptide, is an inhibitory peptide for RGD-mediated adhesion between integrin and extracellular matrix molecules.
Collagen proline hydroxylase inhibitor-1
Collagen proline hydroxylase inhibitor-1 is an antifibroproliferative agents.
LY 117413 is a bio-active chemical，but no detailed information has been published yet.
Cgp 21833 has a thiocarbonylamides structure and it is a potent antifilarial agent under laboratory research stage.
Dihydromyricetin (Ampelopsin, Ampeloptin) is a natural antioxidant flavonoid from Ampelopsis grossedentata.
Phensuximide is an anticonvulsant drug. It can be used for the treatment of neurological disorders stemming from the brain. Phensuximide can suppress the paroxy...
Oxethazaine, an effective topical anesthetic, could be used to relieve the pain caused by peptic ulcer disease and esophagitis.
Dezaguanine is a new antipurine antimetabolite with activity against transplantable rodent leukemias.
CFLZ-171 formic acid salt
CFLZ-171 is an important intermediate to synthesis carfilzomib which is an anti-cancer drug acting as a selective proteasome inhibitor.
Lipid peroxidation inhibitor 1
A lipid peroxidation inhibitor (IC50= 0.07 μM).
Pinoresinol Diglucoside, one of the major lignans with various pharmacological activities, is a sugar lignan which inhibits α-glucosidase in vitro.
The hydrochloride of OTS514. OTS514 is a potent TOPK (T-LAK cell-originated protein kinase) inhibitor (IC50 = 2.6 nM), with an inhibitory effect on small cell l...
Remimazolam, a benzodiazepine derivative, an ultra-short-acting intravenous benzodiazepine sedative/anesthetic, currently in Phase III clinical development for ...
Z-Ile-Glu-Pro-Phe-Ome is a peptide inhibitor of human heart chymase which is a chymotrypsin-like enzyme that converts angiotensin I to angiotensin II.
This active molecular is a bio-active chemical but detailed information has not been published yet.
HMN-154, a novel benzenesulfonamide anticancer drug, inhibits KB (IC50= 0.0026 μg/mL) and colon38 cells (IC50= 0.003 μg/mL).
sulfo-SPDB-DM4 is adrug-linker conjugate for ADC and DM4 with a reactive linker sulfo-SPDB, which can react with antibody to make antibody drug conjugate.
Octodrine is a local anesthetic and vasoconstrictor, shows leucine aminotransferase inhibition.