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Search Results for " drug-like "

20

Compounds

Cat No. Product Name Synonyms Targets
T2620 G-749 G749 Apoptosis , FLT , c-RET , TAM Receptor , Aurora Kinase
G-749, a new-type FLT3 inhibitor, exhibits effective and sustained inhibition of the FLT3 wild type and mutants.
T4697 ABBV-744 ABBV744 Epigenetic Reader Domain , HIV Protease
ABBV-744 is a BDII-selective BET bromodomain inhibitor that inhibits BRD2/3/4. It is used in the research on inflammatory diseases, cancer, and AIDS.
TP1215 Abaloparatide TFA BA 058 TFA,Abaloparatide TFA (247062-33-5 free base),BIM 44058 TFA Others
Abaloparatide TFA (BIM 44058 TFA) is a parathyroid hormone-related protein (PTHrP) analog drug used to treat osteoporosis like the related drug teriparatide.
T8395 Nomegestrol acetate Others , Progesterone Receptor
Nomegestrol acetate is a widely used progestin-like drug,which is characterized as a full agonist at the progesterone receptor
T9623 RORγt inverse agonist 13 ROR
RORγt inverse agonist 13 (Compound 3i) is a potent, orally active and selective RORγt inverse agonist (IC50=63.8 nM), with improved drug-like properties[1].
T2641 KRCA-0008 KRCA 0008,KRCA0008 ACK , ALK
KRCA-0008 is an effective and specific ALK/Ack1 inhibitor (IC50: 12/4 nM); displays drug-like properties without hERG liability.
T21673 N-Isopropylnoratropine Others
N-Isopropylnoratropine is a noratropine derivative and an intermediate in the production of ipratropium, an atropine-like bronchodilator drug via an anticholinergic pathway. N-Isopropylnoratropine is used to examine the ...
T64374 QN523  Autophagy
QN523 represents a novel scaffold with drug-like properties, showing potent in vitro cytotoxicity in a panel of 12 cancer cell lines. QN523 shows significant in vivo efficacy in a pancreatic cancer xenograft model. Autop...
T0383 Fenspiride hydrochloride Fenspiride HCl,Pneumorel,Fluiden,Decaspiride Adrenergic Receptor , PDE , Histamine Receptor
Fenspiride hydrochloride (Decaspiride) , an oxazolidinone spiro compound, is a drug used in the therapy of certain respiratory diseases. It is approved for use in Russia for the therapy of chronic and acute inflammatory ...
T2940 6-Hydroxyflavone 6-HF GABA Receptor
6-Hydroxyflavone (6-HF) is a noncompetitive inhibitors of cytochrome P450 2C9. It is a flavone, a type of chemical compound. It is reported in leaves of Barleria prionitis Linn. (a common Acanthaceae from India). 6-Hydro...
T8873 Bractoppin Others , DNA/RNA Synthesis
Bractoppin is a drug-like inhibitor of phosphopeptide recognition by the human BRCA1 tandem (t)BRCT domain (IC50 = 0.074 μM), which selectively inhibits substrate binding with nanomolar potency in vitro. Structure-activi...
T2836 Isorhamnetin 3-methylquercetin,3'-Methylquercetin,Isorhamnetol,3'-Methoxyquercetin MEK , PI3K , Endogenous Metabolite
Isorhamnetin (3-methylquercetin) is the methylated metabolite of quercetin. Quercetin is an important dietary flavonoid with in vitro antioxidant activity. Isorhamnetin prevents endothelial cell injuries from oxidized LD...
T4978 Sarpogrelate hydrochloride MCI-9042 5-HT Receptor
Sarpogrelate hydrochloride (MCI-9042) , a selective 5-HT2 antagonist, has been widely used as an anti-platelet agent for the treatment of PAD. Target: 5-HT2 Recepter Sarpogrelate is a drug which acts as an antagonist at ...
T16857 SB269652 Others
SB269652 is the first drug-like allosteric modulator of the dopamine D2 receptor.
T24886 TIQ-15 TIQ 15,TIQ15
TIQ-15 is an effective and selective CXCR4 antagonist. It has good drug-like properties.
T25151 Bibrocathol Bibrocathin,Bibrocatholum
Bibrocathol is a well-established antiseptic drug used for the treatment of acute eyelid diseases like blepharitis.
T70007 CT-179
CT-179 is a highly potent and selective small molecule inhibitor of Olig2 with excellent drug-like properties.
T29065 UNC9994 UNC-9994,UNC 9994
UNC9994 is a β-arrestin-biased dopamine D₂ receptor agonist (β-arrestin EC50 = 50 nM; Emax = 97%) with robust in vivo antipsychotic drug-like activities.
T18313 Mc-O-Si(di-iso)-Cl Others
Mc-O-Si(di-iso)-Cl is a cleavable ADC linker, commonly employed in the synthesis of antibody-drug conjugates (ADCs) like Gemcitabine-O-Si(di-iso)-O-Mc [1].
T69613 Ar-H047108 free base
Ar-H047108 free base is an imidazopyridine potassium competitive acid blocker (P-CAB). This drug may be used to treat early stellate cell activation and veno-occlusive-disease (VOD)-like hepatotoxicity.
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