Structure | Cat No. | Product Name | CAS No. | Product Description |
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V60042 | Carboxylesterase-IN-2 | 2764748-88-9 | Carboxylesterase-IN-2 (compound 4u) is a potent Carboxylesterase Notum inhibitor (antagonist) with IC50 less than or equal to 10 nM. |
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V18831 | CRT-0105950 | 1661845-86-8 | CRT0105950 is a potent LIMK inhibitor (antagonist) with IC50s of 0.3 nM and 1 nM for LIMK1 and LIMK2 inhibition, respectively. |
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V12460 | CYM-50769 | 1421365-63-0 | CYM 50769 is a non-peptide selective antagonist of neuropeptide B/W receptor 1 (NPBWR1). |
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V11837 | EN106 | 757192-67-9 | EN106 is a potent FEMIB inhibitor. |
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V36344 | GSK484 free base | 1652629-23-6 | GSK484 is a novel, potent, selective and reversible peptidylarginine deiminase 4 (PAD4) inhibitor which showes high affinity binding to PAD4 with IC50s of 50 nM in the absence of Calcium. |
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V34671 | Hexakis(p-bromophenoxy)cyclotriphosphazene | 4376-72-1 | Hexakis(p-bromophenoxy)cyclotriphosphazene is a useful chemical compound. |
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V60054 | HIF-2α Translation Inhibitor | 882268-69-1 | HIF-2α-IN-4 is a potent HIF-2α translation inhibitor (antagonist) with IC50 of 5 μM. |
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V17133 | IL-17 modulator 4 | 2446803-65-0 | IL-17 modulator 4 is a precursor to IL-17 modulator 1 . |
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V22210 | IN04 | 838816-57-2 | IN04, also know asMethyl 3-(2-((5-(3,5-dimethoxyphenyl)-1,3,4-oxadiazol-2-yl)thio)acetamido)benzoate, is a novel and potent inhibitor of Leucine rich repeat kinase 1 (LRRK1), suppressing osteoclasts (OC) function with no effect on OC formation. |
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V16229 | KN 1022 | 205255-11-4 | KN-1022 also known as1-Piperazinecarboxamide, 4-(6,7-dimethoxy-4-quinazolinyl)-N-(4-nitrophenyl)- is aBioactive molecules. |
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V60064 | Lecithins, egg | 93685-90-6 | Lecithins, egg is a novel and potent. |
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V24834 | OATD-01 | 2088453-21-6 | OATD-01 is a novel, selective andhighly active CHIT1 (chitinase1, hAMCase IC50=9nM, hCHIT1 IC50=26nM) inhibitor with both an excellent PK profile in multiple species and selectivity against a panel of other off-targets. |
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V107935 | Pargeverine hydrochloride | 2765-97-1 | Pargeverine hydrochloride (also known as propinox hydrochloride ) is an antispasmodic compound that has been studied for the treatment of gastrointestinal, uterine, and gallbladder disorders. |
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V34667 | TH-263 | 313520-94-4 | TH-263 is adiaryl sulfonamide derivativeused as anegative control for the type III allosteric LIM-kinase (LIMK) inhibitors TH-257, TH-255 and TH-251. |
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V60041 | WAY-116749 | 380872-69-5 | WAY-116749 also name asEthyl 2-[[2-(3-oxo-2,4-dihydro-1H-quinoxalin-2-yl)acetyl]amino]-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylate |
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V60005 | Follicle-stimulating hormone | 146479-72-3 | Follicle-stimulating hormone (FSH) is a heterodimeric glycoprotein expressed by gonadotrophs in the anterior pituitary. |
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V7876 | Ozagrel sodium | 130952-46-4 | Ozagrel (also known as OKY-046) sodium salt is an antiplatelet agent working as a thromboxane A2 synthesis inhibitor. |
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V107939 | Hydrolyzed collagen (cattle) | 92113-31-0 | |
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V107940 | Collagen hydrolysate(fish) | 92113-31-0 | |
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V17003 | Lasmiditan succinate (COL144, LY573144) | 439239-92-6 | Lasmiditan succinate (COL-144, LY-573144) is a novel and selective 5-HT(1F) receptor agonist with Ki of 2.1 nM versus Ki of 1043 nM and 1357 nM at the 5-HT(1B) and 5-HT(1D) receptors, respectively. |