About 30 results found for searched term "AH1" (0.092 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M3549 | Orlistat | FAS |
| Tetrahydrolipstatin; Ro-18-0647 | ||
| Orlistat is an irreversible inhibitor of pancreatic and gastric lipases with IC50 of 122 ng/ml for PL from human duodenal juice. | ||
| M5775 | Metaxalone | Others |
| AHR438; NSC170959 | ||
| Metaxalone(AHR438; NSC170959) has muscle relaxation function and is an MOR agonist. | ||
| M5921 | Ranitidine hydrochloride | Histamine Receptor |
| AH19065 Hydrochloride | ||
| Ranitidine hydrochloride is a potent, selective and orally active histamine H2-receptor antagonist with an IC50 of 3.3 μM. | ||
| M7594 | AH 11110 | Others |
| α1B-adrenoceptor ligand. | ||
| M7614 | AH13205 | Others |
| AH13205 is a selective, low potency agonist for the EP2 receptor. | ||
| M10600 | SAH-SOS1A TFA | Ras |
| SAH-SOS1A TFA is a peptide-based SOS1/KRAS protein interaction inhibitor. SAH-SOS1A TFA binds to wild-type and mutant KRAS (G12D, G12V, G12C, G12S, and Q61H) with nanomolar affinity (EC50=106-175 nM) and directly and independently blocks nucleotide association. | ||
| M10935 | Tetrahydroxyquinone | ROS |
| Tetrahydroxy-1,4-benzoquinone | ||
| Tetrahydroxyquinone (Tetrahydroxy-1,4-benzoquinone), an anti-cataract agent, is a benzoquinone with redox activity. Tetrahydroxyquinone can participate in the redox cycle with hemiquinone radicals, leading to reactive oxygen species (ROS) formation. | ||
| M13893 | Labetalol | Adrenergic Receptor |
| AH5158; Sch-15719W free base | ||
| Labetalol (AH5158) is an orally active selective α1- and non-selective β-adrenergic receptors competitive antagonist. | ||
| M17657 | 1β,2α,3β,19α-Tetrahydroxy-12-ursen-28-oic acid | Triterpenoids |
| 1β,2α,3β,19α-Tetrahydroxy-12-ursen-28-oic acid | ||
| M17962 | 1,2,3,7-Tetrahydroxy-8-methoxy-6-methyl-9,10-anthracenedione | Others |
| 1,2,3,7-Tetrahydroxy-8-methoxy-6-methyl-9,10-anthracenedione | ||
| M21354 | Recombinant Human SEMA3E (E. coli, N-His) | Other Proteins |
| SEMAH, Semaphorin-3E, SEMA3E, KIAA0331 | ||
| Protein Construct: DNA sequence encoding human SEMA3E (Arg32-Phe516) fused to an N-His tag. accession #: O15041. | ||
| M22340 | FAAH inhibitor 1 | Others |
| FAAH inhibitor 1 | ||
| M22486 | AH-7614 | GPR/FFAR |
| AH7614 | ||
| AH-7614 is a potent and selective FFA4 (GPR120) antagonist, with pIC50s of 7.1, 8.1, and 8.1 for human, mouse, and rat FFA4, respectively. AH-7614 has selectivity for FFA4 over FFA1 (pIC50<4.6). AH-7614 is able to block effects of both the polyunsaturated ω-6 fatty acid linoleic acid and the synthetic FFA4 agonist. | ||
| M25290 | Topsalysin | Others |
| PRX-302; PRX302 PSA-PAH1 | ||
| Topsalysin (PRX-302; PRX302; PSA-PAH1) is a PSA-activated protoxin, a pore-forming protein (synthetic proaerolysin) fusion protein with human prostate-specific antigen. Topsalysin has tumor suppression effect in mice modle. | ||
| M29135 | SAHM1 | Notch |
| SAHM1, a peptide mimetic of a dominant negative form of mastermind-like (MAML), inhibits canonical Notch transcription complex formation. SAHM1 can be used for the research of allergic airway inflammation in mice. | ||
| M29822 | Aha1/Hsp90-IN-1 | Microtubule |
| Aha1/Hsp90-IN-1 (Compound 17) is an Aha1/Hsp90 complex inhibitor. Aha1/Hsp90-IN-1 disrupts Aha1/Hsp90 interactions with an IC50 of 3.32 μM. Aha1/Hsp90-IN-1 inhibits tau aggregation. | ||
| M31064 | SAHM1 TFA | Notch |
| SAHM1 TFA is a Notch pathway inhibitor. SAHM1 TFA stabilizes hydrocarbon-stapled alpha helical peptide. SAHM1 TFA targets the protein-protein interface and prevents Notch complex assembly. | ||
| M41974 | AHR-10037 | COX |
| AHR-10037 is a non-steroidal anti-inflammatory agent with low gastric toxicity. | ||
| M43231 | AH1 | Others |
| AH1 is an immunodominant antigen derived from the gp70 product of an endogenous MuLV. | ||
| M43881 | 1-[4-(Tetrahydro-2,4-dioxo-1(2H)-pyrimidinyl)phenyl]-3-pyrrolidinecarboxaldehyde | Ligand for E3 Ligase |
| 1-[4-(Tetrahydro-2,4-dioxo-1(2H)-pyrimidinyl)phenyl]-3-pyrrolidinecarboxaldehyde | ||
| M43882 | 1-(4-(2,4-Dioxotetrahydropyrimidin-1(2H)-yl)phenyl)piperidine-4-carbaldehyde | Ligand for E3 Ligase |
| 4-Piperidinecarboxaldehyde, 1-[4-(tetrahydro-2,4-dioxo-1(2H)-pyrimidinyl)phenyl]- | ||
| 1-(4-(2,4-Dioxotetrahydropyrimidin-1(2H)-yl)phenyl)piperidine-4-carbaldehyde | ||
| M43884 | 1-[4-(Tetrahydro-2,4-dioxo-1(2H)-pyrimidinyl)phenyl]-4-piperidinecarboxylic acid | Ligand for E3 Ligase |
| 1-[4-(Tetrahydro-2,4-dioxo-1(2H)-pyrimidinyl)phenyl]-4-piperidinecarboxylic acid | ||
| M43887 | 1-(5-(2,4-Dioxotetrahydropyrimidin-1(2H)-yl)pyridin-2-yl)piperidine-4-carbaldehyde | Ligand for E3 Ligase |
| 4-Piperidinecarboxaldehyde, 1-[5-(tetrahydro-2,4-dioxo-1(2H)-pyrimidinyl)-2-pyridinyl]- | ||
| 1-(5-(2,4-Dioxotetrahydropyrimidin-1(2H)-yl)pyridin-2-yl)piperidine-4-carbaldehyde | ||
| M43892 | 3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)-4-fluorobenzoic acid | Ligand for E3 Ligase |
| Benzoic acid, 4-fluoro-3-(tetrahydro-2,4-dioxo-1(2H)-pyrimidinyl)- | ||
| 3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)-4-fluorobenzoic acid | ||
| M44217 | 3,7,23,24-tetrahydroxycucurbita-5,25-dien-19-al | Others |
| 3,7,23,24-tetrahydroxycucurbita-5,25-dien-19-al | ||
| M52462 | Biotin-Ahx-β-Amyloid (1-40) | Amyloid |
| Biotin-Ahx-β-Amyloid (1-40) is a biological active peptide. | ||
| M52472 | Biotinyl-Ahx-Amyloid β-Protein (1-42) | Amyloid |
| Biotinyl-Ahx-Amyloid β-Protein (1-42) is abiotinylated β-Amyloid (1-42), human (TFA). | ||
| M52904 | SAH-SOS1A | Ras |
| SAH-SOS1A is a peptide-based SOS1/KRAS protein interaction inhibitor. | ||
| M53455 | FITC-εAhx-HHV-2 Envelope Glycoprotein G (561-578) | Anti-infection |
| FITC-εAhx-HHV-2 Envelope Glycoprotein G (561-578) is a FITC labeled HHV-2 Envelope Glycoprotein G (561-578). | ||
| M54798 | 1,2,3,4-Tetrahydronorharman-1-one | Anti-infection |
| 1,2,3,4-Tetrahydronorharman-1-one is a manzamine alkaloid with activity against infectious and tropical parasitic diseases from an Indonesian sponge. | ||
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