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Thalidomide-O-amido-PEG2-C2-NH2 (TFA)
Catalog No. A21634 E3 ligase ligand-linker conjugateThalidomide-O-amido-PEG2-C2-NH2 TFA is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and 2-unit PEG linker used in PROTAC technology. 了解更多 -
Mirogabalin
Catalog No. A21626 Mirogabalin (DS-5565) is a novel, preferentially selective α2δ-1 ligand characterized by high potency and selectivity to the α2δ-1 subunit of voltage-sensitive calcium channel complexes in the CNS. 了解更多 -
Nanatinostat
Catalog No. A21625 HDAC inhibitorNanatinostat (CHR-3996) is a potent, class I selective and orally active histone deacetylase (HDAC) inhibitor with an IC50 of 8 nM. 了解更多 -
Pardoprunox hydrochloride
Catalog No. A21624 partial dopamine D2 and D3 receptor agonistPardoprunox hydrochloride is a novel partial dopamine D2 and D3 receptor agonist and serotonin 5-HT1A receptor agonist, D2 (pKi = 8.1) and D3 receptor (pKi = 8.6) partial agonist and 5-HT1A receptor (pKi = 8.5) full agonist. 了解更多 -
Acetoacetic acid sodium salt
Catalog No. A21621 Acetoacetic acid sodium salt is a metabolite of non-esterified fatty acids, involved in the development of human diabetes. Acetoacetic acid sodium salt induces oxidative stress to inhibit the assembly of very low density lipoprotein in bovine hepatocytes. 了解更多 -
Dasotraline
Catalog No. A21618 triple reuptake inhibitorDasotraline is a triple reuptake inhibitor that blocks dopamine, norepinephrine, and serotonin transporters with IC50 values of 4, 6, and 11 nM, respectively. 了解更多 -
Ecteinascidin-Analog-1
Catalog No. A21614 Ecteinascidin-Analog-1 is a useful intermediate for chemical sythesis of Ecteinascidin analogues; Ecteinascidins is a family of tetrahydroisoquinoline alkaloids with wide range of antitumor and antimicrobial activities. 了解更多 -
Cyantraniliprole D3
Catalog No. A21610 Cyantraniliprole D3 is the deuterium labeled Cyantraniliprole, which is an insecticide of the ryanoid class. 了解更多 -
Norepinephrine hydrochloride
Catalog No. A21605 β1-selective adrenergic receptor agonistNorepinephrine hydrochloride (Levarterenol hydrochloride; L-Noradrenaline hydrochloride) is a β1-selective adrenergic receptor agonist with EC50 of 5.37 μM. 了解更多 -
5-Hydroxy Propafenone D5 Hydrochloride
Catalog No. A21604 5-Hydroxy Propafenone D5 Hcl is the deuterium labeled 5-Hydroxy Propafenone. 了解更多 -
BAY1217389
Catalog No. A21595 MPS1 kinase inhibitorBAY 1217389 is a potent, and selective inhibitor of the monopolar spindle 1 (MPS1) kinase with an IC50 value less than 10 nM. 了解更多 -
Notch inhibitor 1
Catalog No. A21591 Notch inhibitorNotch inhibitor 1 is a potent Notch inhibitor, with IC50s of 7.8 and 8.5 nM for Notch 1 and Notch 3, respectively. Used in the research of cancer. 了解更多 -
Bupropion morpholinol D6
Catalog No. A21587 Bupropion morpholinol D6 is a useful labeled metabolite of Bupropion. 了解更多 -
EHNA hydrochloride
Catalog No. A21585 Adenosine deaminase inhibitorEHNA hydrochloride is a specific inhibitor of adenosine deaminase, prevents dAdo degradation and increases mitochondrial dATP levels in fibroblasts. 了解更多 -
Ipragliflozin L-Proline
Catalog No. A21579 SGLT2 inhibitorIpragliflozin (L-Proline) is a highly potent and selective SGLT2 inhibitor with an IC50 of 2.8 nM; little and NO potency for SGLT1/3/4/5/6. 了解更多 -
SCH 546738
Catalog No. A21554 CXCR3 antagonistSCH 546738 is a potent, orally active and non-competitive CXCR3 antagonist, the affinity constant (Ki) of SCH 546738 binding to human CXCR3 receptor is determined to be 0.4 nM in multiple experiments. 了解更多 -
Gusperimus trihydrochloride
Catalog No. A21551 Gusperimus trihydrochloride (Spanidin) is a derivative of the antitumor antibiotic spergualin with immunosuppressant activity. 了解更多 -
BMS-983970
Catalog No. A21547 pan-Notch inhibitorBMS-983970 is an oral pan-Notch inhibitor for the treatment of multiplecancers. 了解更多 -
Diethyl aminoethyl hexanoate citrate
Catalog No. A21544 plant growth regulatorDiethyl aminoethyl hexanoate citrate is a compound that is widely used as a plant growth regulator. 了解更多 -
Omadacycline hydrochloride
Catalog No. A21540 Omadacycline hydrochloride is novel, aminomethyl tetracycline antibiotic being developed for the treatment of community-acquired bacterial infections. The ED50 for Escherichia coli is 2.02 mg/kg. 了解更多 -
Taribavirin
Catalog No. A21525 inosine monophosphate dehydrogenase inhibitorTaribavirin is an orally active inosine monophosphate dehydrogenase inhibitor, has activity against a wide range of viruses, especially the hepatitis C virus and influenza virus. 了解更多 -
(S)-(-)-Citronellal
Catalog No. A21520 (S)-(-)-Citronellal ((-)-Citronellal) is a monoterpenoid compound found in Corymbia citriodora and Cymbopogon nardus essential oils. 了解更多 -
5'-GTP trisodium salt hydrate
Catalog No. A21514 signal transducing G proteins activator5'-GTP trisodium salt hydrate is an activator of the signal transducing G proteins and also serves as an energy-rich precursor of mononucleotide units in the enzymatic biosynthesis of DNA and RNA. 了解更多 -
Beclabuvir
Catalog No. A21511 HCV NS5B RNA-dependent RNA polymerase inhibitorBeclabuvir is an allosteric inhibitor that binds to thumb site 1 of the hepatitis C virus (HCV) NS5B RNA-dependent RNA polymerase, and inhibits recombinant NS5B proteins from HCV genotypes 1, 3, 4, and 5 with IC50 of < 28 nM. 了解更多 -
Tecarfarin sodium
Catalog No. A21509 VKOR antagonistTecarfarin sodium (ATI-5923 sodium) is a novel orally active non-competitive vitamin K epoxide reductase (VKOR) antagonist, impairs the activation of the vitamin K-dependent clotting factors II, VII, IX and X. 了解更多 -
Rhosin
Catalog No. A21504 RhoA subfamily Rho GTPases inhibitorRhosin is a potent, specific RhoA subfamily Rho GTPases inhibitor, which specifically binds to RhoA to inhibit RhoA-GEF interaction with a Kd of ~ 0.4 uM, and does not interact with Cdc42 or Rac1, nor the GEF, LARG. Rhosin induces cell apoptosis. 了解更多 -
Prinomastat
Catalog No. A21501 metalloproteinase inhibitorPrinomastat (AG3340) is a broad spectrum, potent, orally active metalloproteinase (MMP) inhibitor with IC50s of 79, 6.3 and 5.0 nM for MMP-1, MMP-3 and MMP-9, respectively. 了解更多 -
UAA crosslinker 1 hydrochloride
Catalog No. A21496 UAA crosslinker 1 hydrochloride is an amber codon used for non-canonical amino acids (ncAAs) incorporation. The ncAAs can be incorporated into proteins in vivo by making use of the promiscuous activity of certain wildtype and engineered aminoacyl-tRNA synthetases. 了解更多 -
Docebenone
Catalog No. A21493 5-LO (5-lipoxygenase) inhibitorDocebenone (AA 861) is a potent, selective and orally active 5-LO (5-lipoxygenase) inhibitor. 了解更多 -
Macozinone
Catalog No. A21488 DprE inhibitorMacozinone (PBTZ169) is a bactericidal benzothiazinone and a potent DprE1 (decaprenylphosphoryl-β-d-ribose 2??-oxidase) inhibitor. 了解更多 -
Givinostat hydrochloride
Catalog No. A21487 HDAC inhibitorGivinostat hydrochloride (ITF-2357 hydrochloride) is a HDAC inhibitor with an IC50 of 198 and 157 nM for HDAC1 and HDAC3, respectively. 了解更多 -
Delavirdine
Catalog No. A21469 non-nucleoside reverse transcriptase inhibitorDelavirdine(U 90152) is a potent non-nucleoside reverse transcriptase inhibitor (NNRTI). 了解更多 -
β-Apo-13-carotenone D3
Catalog No. A21462 RXRα antagonistβ-Apo-13-carotenone D3 is the deuterium labeled β-Apo-13-carotenone. β-Apo-13-carotenone (D'Orenone) is a naturally occurring β-apocarotenoid functioned as an antagonist of RXRα. 了解更多 -
Betamethasone hydrochloride
Catalog No. A21455 Betamethasone (hydrochloride) is a glucocorticoid steroid with anti-inflammatory and immunosuppressive properties. 了解更多 -
(-)-Talarozole
Catalog No. A21451 retinoic acid metabolism inhibitor(-)-Talarozole is a potent inhibitor of retinoic acid metabolism extracted from patent WO 1997049704 A1. 了解更多
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