|Description||Ombrabulin hydrochloride is the hydrochloride salt form of Ombrabulin. Ombrabulin, also called as AVE8062, a synthetic water-soluble analogue of CA-4-P, binds to the colchicine binding site of endothelial cell tubulin, and induces G2/M arrest, thus bringi|
|Synonyms||2-amino-3-hydroxy-N-[2-methoxy-5-[2-(3,4,5-trimethoxyphenyl)ethenyl]phenyl]propanamide;hydrochloride 253426-24-3 (S)-N-(5-(3,4,5-TRIMETHOXYSTYRYL)-2-METHOXYPHENYL)-2-AMINO-3-HYDROXYPROPANAMIDE HYDROCHLORIDE A817797 2-amino-3-hydroxy-N-[2-methoxy-5-[2-(3,4|
|Solubility||Soluble to 10 mM in H2O|
|Storage||Store in a cool and dry place and at 0 - 4℃ for short term (days to weeks) or -128℃ for long term (months to years).|
|Shelf Life||2 years|
Sancycline is a tetracycline bacteriostatic antibiotic which can bind to the Tet repressor protein (TetR). It is a rare semi-synthetic tetracycline prepared by ...
AR-7, also known as Atypical retinoid 7, was developed as a highly potent and selective enhancer of the chaperone-mediated autophagy (CMA) through antagonizing ...
Minocycline is a broad-spectrum tetracycline antibiotic, which has a broader spectrum than the other members of the group. It has a 7-dimethylamino and lacking ...
Yunaconitine is a highly toxic aconitum alkaloid.
The hydrochloride salt form of Emixustat which could effectively inhibit the production of 11-cis-retinol which is related to age-related macular degeneration.
Valrubicin (AD-32) is a chemotherapy drug used to treat bladder cancer. It is a semisynthetic analog of the anthracycline doxorubicin, and is administered by in...
GSK2837808A is a potent and specific lactate dehydrogenase A (LDHA) with IC50values of 1.9 and 14 nM for LDHA and LDHB, respectively and inhibits lactate produc...
Notoginsenoside R1 is extracted from the roots of Panax notoginseng (Burk.)F.H.Chen. It has some neuronal protective, antihypertensive effects and exhibits anti...
Cromolyn, a chromene derivative, could be used in the treatmen of allergic an a aast cell stabiliser.
A 438079 hydrochloride
A 438079 hydrochloride is a competitive P2X7 receptor antagonist with pIC50 value of 6.9 for the inhibition of Ca2+ influx in the human recombinant P2X7 cell li...
Mas7, a structural analogue of mastoparan, is G protein activator via Gαi and Gαo stimulation.
GSK299115A is a G-Protein-Coupled Receptor Kinase 2 (GRK2) Inhibitor.
STK16-IN-1, a pyrrolonaphthyridinone compound, only potently inhibited STK16 (relative activity remaining 0.65%) and mTOR (relative activity remaining 0.4%) at ...
This active molecular is a potent purine nucleoside phosphorylase inhibitor and a T cell-selective immunosuppressive agent. CI-972 inhibited proliferation of hu...
Aminophenazone (or aminopyrine) is a pyrazolone with analgesic, anti-inflammatory, and antipyretic properties but has risk of agranulocytosis.
Dihydrokavain is a kavalactone source from kava beverages used in herbal medicine to treat sleep disturbances, as well as stress and anxiety.
This molecular is a prodrug of ACT-246475 which is a selective P2Y12 receptor antagonist with a wider therapeutic window in the rat model. ACT-281959 is the pho...
Cyclo(RADfK) is a selective α(v)β(3) integrin ligand. It has been used for research, therapy, and diagnosis of neoangiogenesis. It is also used as a negative co...
As A very potent uncoupler of oxidative phosphorylation in mitochondria, FCCP transports protons across cell membranes which disrupts ATP synthesis,