Others

(R)-OR-S1 is a SAM-competitive, highly selective, orally bioavailable dual inhibitor of EZH1/2.

Acorafloxacin is a broad-spectrum fluoroquinolone antibacterial drug being developed for the treatment of acute bacterial skin and skin structure infections and community-acquired pneumonia.

Gastrazole is a CCK2 receptor antagonist potentially. It also used for the treatment of pancreatic cancer.

Aclantate is a nonsteroidal anti-inflammatory drug.

AFP-07 is a highly selective and potent agonist. It was used for the prostacyclin receptor.

A457 is an antagonist of the prokineticin receptor.

8-CSC is a dual agent endowed with good hMAO-B inhibitory activity (Ki: 235 nM in baboon liver mitochondria) and A2A affinity (Ki: 36 nM in rat brain striatal membranes receptor).

A-424274 is a positive allosteric modulator of α4β2 neuronal nicotinic receptor.

A1B11 is a selective SIRT2 inhibitor.

Aganodine is a guanidine that activates presynaptic imidazoline receptors. Aganodine inhibits the presynaptic release of norepinephrine through its agonism at imidazoline receptors.

YLT192 is an orally active and bioavailable VEGFR2 inhibitor. It also has potent antiangiogenic activity and antitumor efficacy.

Propargyl-PEG2-methylamine is a PEG derivative containing a propargyl group and methylamine group. PEG Linkers are useful in the development of antibody-drug conjugates.

Prumycin dihydrochloride is an agent of antifungal antibiotic.

PSB-6426 is the first potent and selective human nucleoside triphosphate diphosphohydrolase-2 inhibitor.

p18SMI-21 is a novel INK4C inhibitor. It also specifically blocking the bioactivity of p18 protein.

PDE5-IN-6c is a potent and selective inhibitor of PDE5A1.

biotinylated anandamide analog acts as a probe for visualizing the accumulation and intracellular trafficking of anandamide

Q-VD-OPh (quinolyl-valyl-O-methylaspartyl-[-2,6-difluorophenoxy]-methyl ketone) is a broad-spectrum caspase inhibitor, provides a cost-effective, non-toxic, and highly specific means of apoptotic inhibition and provides new insight into the design of new

group I metabotropic glutamate receptor antagonist and group II mGlu agonist

(R)-4-Carboxyphenylglycine is a NMDA receptor antagonist.

Dacomitinib metabolite M2 is also known as Dacomitinib cysteine conjugate. Dacomitinib inhibits both the wild-type (WT) EGFR and EGFR T790M.

Dacemazine is a phenothiazine derivative that acts as a histamine antagonist at the H1 subtype. It was also assessed as a possible anticancer drug.

Flumethasone 21-acetate is an anti-inflammatory corticosteroid.

BSBM6 is an inhibitor of Aβ aggregation and neuronal toxicity that acts by reversing the aggregation and toxicity of amyloid-β peptides.

BI1002494 is an effective and selective Syk inhibitor.

L 158338 is an antagonist of the angiotensin receptor.

Butaclamol is a typical antipsychotic which was never marketed. It also acts as a dopamine receptor antagonist.

LY2048978 is an effective and orally-bioavailable antagonist of kappa-selective. It has activity in animal models predictive of efficacy in mood and addictive disorders.

HENA is a novel activator of large conductance, voltage- and Ca2+-gated K+ (BK) channels.

Ornidazole diol is a diol produced through ornidazole rapidly hydrolyzing in basic solutions.

Heptaibin 是一种有用的有机化合物，可用于生命科学领域的相关研究。其产品编号为 T125107，CAS号为 291311-47-2。

2-Chloronaphthalene is an organochlorine chemical compound and is a chlorinated derivative of naphthalene. The compound is an isomer for 1-chloronaphthalene.

Bekanamycin sulfate is an agent of bioactive chemicals.

Homocarbonyltopsentin is a small-molecule TSL2-binding compound, binds to pentaloop conformations of TSL2 and promotes a shift to triloop conformations that display enhanced SMN2 exon 7 (E7) splicing (EC50: 16 μM).

Etoricoxib HCl is a synthetic, nonsteroidal anti-inflammatory drug. Etoricoxib specifically binds to and inhibits the enzyme cyclooxygenase-2, resulting in inhibition of the conversion of arachidonic acid into prostaglandins.

Conjugated estrogens are medicine that contains a mixture of estrogen hormones. It is used to treat moderate to severe hot flashes, changes in and around the vagina, and other symptoms of menopause or low amounts of estrogen. Conjugated estrogens tablet i