MedChemExpress MCE - Products
MedChemExpress (MCE) offers a wide range of high-quality research chemicals and biochemicals (novel life-science reagents, reference compounds and natural compounds) for scientific use.
| Product | Description | |
|---|---|---|
| IM-2 | IM-2 is an ADC linker used in the synthesis of antibody-drug conjugates (ADCs) [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2813269-89-3. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-160157. |  |
| IM-250 | IM-250 is an orally active helicase-primase inhibitor. IM-250 is effective against HSV infection. IM-250 inhibits HSV-1 infection in Vero cells (IC 50 : ~20 nM) [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2305750-23-4. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-150306. | |
| IMAB027 | IMAB027 (ASP1650) is a specific anti- CLDN6 mAb, while CLDN6 ( Claudin 6 ) is a tight junction membrane protein, aberrantly expressed in various human cancer types, ovarian cancers particularly. IMAB 027 shows anti-tumor activity, and induces apoptosis in CLDN6 + ovarian and testicular cancer cell lines [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: ASP1650. CAS No. 1650599-68-0. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99413. | |
| Imaradenant | AZD4635 (HTL1071) is a potent, selective and orally active adenosine A2A receptor ( A2AR ) antagonist. AZD4635 binds to human A2AR with a K i of 1.7 nM and shows >30-fold selectivity over other adenosine receptors [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: HTL1071; AZD4635. CAS No. 1321514-06-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-101980. | |
| Imatinib | Imatinib (STI571) is an orally bioavailable tyrosine kinases inhibitor that selectively inhibits BCR/ABL , v-Abl , PDGFR and c-kit kinase activity. Imatinib (STI571) works by binding close to the ATP binding site, locking it in a closed or self-inhibited conformation, therefore inhibiting the enzyme activity of the protein semicompetitively [1] [2] [3] [4]. Imatinib also is an inhibitor of SARS-CoV and MERS-CoV [5]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: STI571; CGP-57148B. CAS No. 152459-95-5. Pack Sizes: 10 mM * 1 mL; 200 mg; 500 mg; 1 g; 5 g. Product ID: HY-15463. | |
| Imatinib Mesylate | Imatinib Mesylate (STI571 Mesylate) is a tyrosine kinases inhibitor that inhibits c-Kit , Bcr-Abl , and PDGFR ( IC 50 =100 nM) tyrosine kinases. Uses: Scientific research. Group: Signaling pathways. Alternative Names: STI571 Mesylate; CGP-57148B Mesylate. CAS No. 220127-57-1. Pack Sizes: 10 mM * 1 mL; 200 mg; 500 mg; 1 g; 5 g. Product ID: HY-50946. | |
| Imazalil | Imazalil (Enilconazole) is a fungicide. Imazalil has oral activity and strongly activates mPXR but not mCAR in mouse liver. Imazalil is commonly used to protect various agricultural crops against fungal attack. Imazalil induces developmental abnormalities, gut microbiota dysbiosis, and hepatic metabolism disorder [1] [2] [3]. Uses: Scientific research. Group: Natural products. Alternative Names: Enilconazole. CAS No. 35554-44-0. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg; 1 g; 5 g; 10 g. Product ID: HY-B1134. | |
| Imazamox | Imazamox (CL29926) is a systemic herbicide that inhibits the production of acetolactate synthase (ALS) in plants with high selectivity, high activity, safety and broadspectrum activity, which would then inhibit plant growth and ultimately lead to plant death [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CL29926; (±)-Imazamox. CAS No. 114311-32-9. Pack Sizes: 10 mM * 1 mL; 10 mg; 50 mg; 100 mg. Product ID: HY-100427. | |
| Imazapic | Imazapic is a selective herbicide used to control perennial grasses and some broadleaf weeds. Uses: Scientific research. Group: Signaling pathways. CAS No. 104098-48-8. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-B1860. | |
| Imazethapyr | Imazethapyr is an imidazolinone herbicide used in crops. Imazethapyr can protect crops from damage by weeds and annual grasses [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 81335-77-5. Pack Sizes: 10 mM * 1 mL; 50 mg. Product ID: HY-133188. | |
| IMD-0354 | IMD-0354 (IKK2 Inhibitor V) is a selective IKKβ inhibitor which inhibits NF-κB activity [1]. IMD0354 inhibits TNF-α induced NF-κB transcription activity with an IC 50 of 1.2 uM [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: IKK2 Inhibitor V. CAS No. 978-62-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-10172. | |
| Imdevimab | Imdevimab (REGN10987) is a human monoclonal antibody to target SARS-CoV-2 virus, which causes COVID-19. Imdevimab lacks efficacy against COVID-19 variants. Imdevimab can be used in combination with Casirivimab (HY-P99341), it reduces viral load and improves diseases [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: REGN10987. CAS No. 2415933-40-1. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99342. | |
| iMDK | iMDK is a potent PI3K inhibitor and inhibits the growth factor MDK (also known as midkine or MK). iMDK suppresses non-small cell lung cancer (NSCLC) cooperatively with A MEK inhibitor without harming normal cells and mice[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 881970-80-5. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-110171. | |
| Imeglimin hydrochloride | Imeglimin hydrochloride (EMD 387008) is an oral glucose-lowering agent. Imeglimin also reduces reactive oxygen species ( ROS ) production, increases mitochondrial DNA and improves mitochondrial function [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: EMD 387008 hydrochloride. CAS No. 775351-61-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-14771A. | |
| Imepitoin | Imepitoin (AWD 131-138) is a new low-affinity partial benzodiazepine receptor agonist with potent anticonvulsant and anxiolytic properties in rodent models. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AWD 131-138. CAS No. 188116-07-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-14953. | |
| Imexon | Imexon (BM 06002) is an iminopyrrolidone aziridine with anti-cancer activity. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BM 06002. CAS No. 59643-91-3. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-15385. | |
| Imgatuzumab | Imgatuzumab (RG 7160) is a humanized monoclonal antibody against the EGFR. Imgatuzumab acts as an immunomodulator. Imgatuzumab can be used in research of cancer [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: RG 7160; RO 5083945; Anti-EGFR Recombinant Antibody. CAS No. 959963-46-3. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99295. | |
| Imidacloprid | Imidacloprid is an effective and widely used neonicotinoid pesticide to control pests of cereals, vegetables, tea and cotton. Uses: Scientific research. Group: Signaling pathways. CAS No. 138261-41-3. Pack Sizes: 10 mM * 1 mL; 100 mg; 200 mg; 500 mg. Product ID: HY-B0838. | |
| Imidafenacin | Imidafenacin (KRP-197; ONO-8025) is a potent and selective inhibitor of M3 receptors. Uses: Scientific research. Group: Signaling pathways. Alternative Names: KRP-197; ONO-8025. CAS No. 170105-16-5. Pack Sizes: 10 mM * 1 mL; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0662. | |
| Imidapril | Imidapril (TA-6366 free base) is an orally active angiotensin-converting enzyme (ACE) and MMP-9 inhibitor. Imidapril suppresses the conversion of angiotensin I to angiotensin II and thereby reduces total peripheral resistance and systemic blood pressure. Imidapril can be used for hypertension, type 1 diabetic, nephropathy and chronic heart failure research [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: TA-6366 free base. CAS No. 89371-37-9. Pack Sizes: 5 mg; 10 mg. Product ID: HY-B1451A. | |
| Imidapril hydrochloride | Imidapril hydrochloride (TA-6366) is an orally active angiotensin-converting enzyme (ACE) and MMP-9 inhibitor. Imidapril hydrochloride suppresses the conversion of angiotensin I to angiotensin II and thereby reduces total peripheral resistance and systemic blood pressure. Imidapril hydrochloride can be used for hypertension, type 1 diabetic, nephropathy and chronic heart failure research [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: TA-6366. CAS No. 89396-94-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B1451. | |
| Imidazenil | Imidazenil is a partial positive allosteric modulator of GABA A receptors with anxiolytic, antipanic and anticonvulsant activities. Uses: Scientific research. Group: Signaling pathways. CAS No. 151271-08-8. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-121393. | |
| Imidazol-1-yl-acetic acid | Imidazol-1-yl-acetic acid is an endogenous metabolite. Uses: Scientific research. Group: Natural products. CAS No. 22884-10-2. Pack Sizes: 500 mg; 1 g. Product ID: HY-W010448. | |
| Imidazole | Imidazole (Glyoxaline; 1,3-Diaza-2,4-cyclopentadiene) is a heterocyclic aromatic compound. Imidazole bearing molecules have been used as corrosion, acetylcholinesterase (AChEI) and xanthine oxidase (XO) inhibitors, performing biological activities such as antifungal, antituberculosis, anti-inflammatory, antioxidant, and analgesic, amongst many others. Imidazole inhibits the enzymatic conversion of the endoperoxides (PGG 2 and PGH 2 ) to thromboxane A2 by platelet microsomes. Imidazole derivatives exhibits inhibition on SARS-CoV-2 3CL Pro enzyme, which is promising for research in the field of Alzheimers disease, gout, COVID-19 and thrombo-embolic disease [1] [2] [3]. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: Glyoxaline; 1,3-Diaza-2,4-cyclopentadiene. CAS No. 288-32-4. Pack Sizes: 10 mM * 1 mL; 5 g. Product ID: HY-D0837. | |
| Imidazoleacetic acid | Imidazoleacetic acid is an endogenous ligand that stimulates imidazole receptors. Uses: Scientific research. Group: Natural products. Alternative Names: Imidazolyl-4-acetic acid. CAS No. 645-65-8. Pack Sizes: 10 mg; 25 mg; 50 mg. Product ID: HY-113413. | |
| Imidazoleacetic acid hydrochloride | Imidazoleacetic acid hydrochloride is a γ-aminobutyric acid receptor agonist. Imidazoleacetic acid hydrochloride inhibits GABA-T in a non-competitive manner, with a K i value of 0.34 mM. Imidazoleacetic acid hydrochloride increases total free GABA in brain [1] [2] [3]. Uses: Scientific research. Group: Natural products. Alternative Names: Imidazolyl-4-acetic acid hydrochloride. CAS No. 3251-69-2. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g. Product ID: HY-W007686. | |
| Imidazole ketone erastin | Imidazole ketone erastin is a potent, selective, and metabolically stable inhibitor of the cystine-glutamate antiporter, system xc- and an activator of ferroptosis. Imidazole ketone erastin has anti-tumor activity[1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: IKE. CAS No. 1801530-11-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-114481. | |
| Imidazolidinyl urea | Imidazolidinyl urea is a commonly used antibacterial preservative in cosmetics and pharmaceuticals that releases formaldehyde through decomposition. Imidazolidinyl urea can also be used in the preparation of multifunctional hydrogels for the care of infectious wounds. Imidazolidinyl urea has broad-spectrum antibacterial activity, which mainly inhibits the reproduction of gram-negative bacteria and gram-positive bacteria, and restricts the growth of yeast and mold to a certain extent. Imidazolidinyl urea can induce non-histaminergic allergy by MRGPRX2 activation of mast cells [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 39236-46-9. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g. Product ID: HY-B1158. | |
| Imidocarb | Imidocarb is a potent antiprotozoal agent. Imidocarb is active against the parasite B. bovis with an IC 50 of 87 μg/mL [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 27885-92-3. Pack Sizes: 10 mM * 1 mL; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-135611. | |
| Imidocarb dipropionate | Imidocarb dipropionate is a potent antiprotozoal agent. Imidocarb dipropionate is active against the parasite B. bovis with an IC 50 of 87 μg/mL [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 55750-06-6. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-107496. | |
| Iminodiacetic acid | Iminodiacetic acid (IDA) is a chelating agent that strongly binds transition metals [1]. Iminodiacetic acid can be used for removal of toxic metal ions from water [2]. Iminodiacetic acid can serve as a biomarker to potentially predict the severity of ARDS (acute respiratory distress syndrome) [3]. Uses: Scientific research. Group: Natural products. CAS No. 142-73-4. Pack Sizes: 10 mM * 1 mL; 5 g; 10 g. Product ID: HY-W012683. | |
| Iminodibenzyl | Iminodibenzyl is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 494-19-9. Pack Sizes: 10 mM * 1 mL; 25 g. Product ID: HY-B2131. | |
| Iminostilbene | Iminostilbene is a chemical precursor of carbamazepine. Additionally, Iminostilbene is an orally active inhibitor of PKM2 (Pyruvate Kinase M2) and COX2 (Cyclooxygenase-2). Iminostilbene exerts its effects by inhibiting PKM2 and its interaction with HIF-1α and STAT3 , reducing COX2 and iNOS expression, and decreasing LPS-induced release of IL-1β , IL-6 , TNF-α , and MCP-1 , thereby suppressing macrophage-mediated inflammatory responses and improving myocardial ischemia/reperfusion (MI/R) injury. Iminostilbene holds promise for research in inflammation regulation, cardiovascular diseases (such as MI/R injury), and macrophage-mediated immune-related diseases [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 256-96-2. Pack Sizes: 10 mM * 1 mL; 500 mg. Product ID: HY-N7064. | |
| Imipenem | Imipenem (MK0787), a stable crystalline derivative of thienamycin, is an antibiotic and has the excellent activity against a broad range of gram-positive and gram-negative aerobic and anaerobic bacteria. Imipenem can be used for the research of carbapenem-nonsusceptible and P. aeruginosa biofilm infections [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: N-Formimidoyl thienamycin; MK0787. CAS No. 64221-86-9. Pack Sizes: 25 mg; 50 mg; 100 mg. Product ID: HY-B1369A. | |
| Imipenem monohydrate | Imipenem monohydrate, a stable crystalline derivative of thienamycin, is an antibiotic and has the excellent activity against a broad range of gram-positive and gram-negative aerobic and anaerobic bacteria. Imipenem monohydrate can be used for the research of carbapenem-nonsusceptible and P. aeruginosa biofilm infections [1] [2] [3]. Uses: Scientific research. Group: Natural products. Alternative Names: N-Formimidoyl thienamycin monohydrate; MK0787 monohydrate. CAS No. 74431-23-5. Pack Sizes: 25 mg; 50 mg; 100 mg; 500 mg. Product ID: HY-B1369. | |
| Imipramine | Imipramine is an orally active tertiary amine tricyclic antidepressant. Imipramine is a Fascin1 inhibitor with antitumor activities. Imipramine also inhibits serotonin transporter with an IC 50 value of 32 nM. Imipramine stimulates U-87MG glioma cells autophagy and induces HL-60 cell apoptosis. Imipramine shows neuroprotective and immunomodulatory effects [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Signaling pathways. CAS No. 50-49-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B1490A. | |
| Imipramine-d4 hydrochloride | Imipramine-d 4 (hydrochloride) is the deuterium labeled Imipramine hydrochloride. Imipramine hydrochloride is an orally active tertiary amine tricyclic antidepressant. Imipramine hydrochloride is a Fascin1 inhibitor with antitumor activities. Imipramine hydrochloride also inhibits serotonin transporter with an IC50 value of 32 nM. Imipramine hydrochloride stimulates U-87MG glioma cells autophagy and induces HL-60 cell apoptosis. Imipramine hydrochloride shows neuroprotective and immunomodulatory effects[1][2][3][4][5][6]. Uses: Scientific research. Group: Isotope-labeled compounds. CAS No. 61361-33-9. Pack Sizes: 1 mg. Product ID: HY-B1490S. | |
| Imipramine hydrochloride | Imipramine hydrochloride is an orally active tertiary amine tricyclic antidepressant. Imipramine hydrochloride is a Fascin1 inhibitor with antitumor activities. Imipramine hydrochloride also inhibits serotonin transporter with an IC 50 value of 32 nM. Imipramine hydrochloride stimulates U-87MG glioma cells autophagy and induces HL-60 cell apoptosis. Imipramine hydrochloride shows neuroprotective and immunomodulatory effects [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Signaling pathways. CAS No. 113-52-0. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-B1490. | |
| Imiquimod | Imiquimod (R 837), an immune response modifier, is a selective toll like receptor 7 (TLR7) agonist. Imiquimod exhibits antiviral and antitumor effects in vivo. Imiquimod can be used for the research of external genital, perianal warts, cancer and COVID-19 [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: R 837. CAS No. 99011-02-6. Pack Sizes: 100 mg; 200 mg; 500 mg. Product ID: HY-B0180. | |
| Imiquimod hydrochloride | Imiquimod hydrochloride (R 837 hydrochloride), an immune response modifier, is a selective toll like receptor 7 (TLR7) agonist. Imiquimod hydrochloride exhibits antiviral and antitumor effects in vivo. Imiquimod hydrochloride can be used for the research of external genital, perianal warts, cancer and COVID-19 [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: R 837 hydrochloride. CAS No. 99011-78-6. Pack Sizes: 10 mM * 1 mL; 100 mg; 200 mg; 500 mg. Product ID: HY-B0180A. | |
| Imiquimod maleate | Imiquimod maleate (R 837 maleate), an immune response modifier, is a selective toll like receptor 7 (TLR7) agonist. Imiquimod maleate exhibits antiviral and antitumor effects in vivo. Imiquimod maleate can be used for the research of external genital, perianal warts, cancer and COVID-19 [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: R 837 maleate. CAS No. 896106-16-4. Pack Sizes: 10 mM * 1 mL; 100 mg; 200 mg; 500 mg. Product ID: HY-B0180B. | |
| Imlunestrant | Imlunestrant (LY-3484356) is an orally active, potent and selective estrogen receptor degrader (SERD) with pure antagonistic properties. Imlunestrant results in sustained inhibition of ER-dependent gene transcription and cell growth. Imlunestrant can be used for the research of ER-positive (ER+) advanced breast cancer (aBC) and endometrial endometrioid cancer (EEC) [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: LY-3484356. CAS No. 2408840-26-4. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-145572. | |
| Imlunestrant tosylate | Imlunestrant (LY-3484356) tosylate is an orally active, potent and selective estrogen receptor degrader (SERD) with pure antagonistic properties. Imlunestrant tosylate results in sustained inhibition of ER-dependent gene transcription and cell growth. Imlunestrant tosylate can be used for the research of ER-positive (ER+) advanced breast cancer (aBC) and endometrial endometrioid cancer (EEC) [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: LY-3484356 tosylate. CAS No. 2408840-41-3. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-145572A. | |
| IMM-01 | IMM-01 is a mammalian Diaphanous (mDia)-related formins agonist that inhibits DID-DAD (diaphanous inhibitory domain-diaphanous autoregulatory domain) binding with an IC 50 of 140 nM. IMM-01 acts by disrupting the autoinhibitory bond between the DID and DAD domain and thus activates formins. IMM-01 shows anticancer effects [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 218795-74-5. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-124808. | |
| Immepip dihydrobromide | Immepip dihydrobromide is a H3 agonist. Immepip dihydrobromide can reduce cortical histamine release. Immepip dihydrobromide can be used for the research of neurological diseases [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 164391-47-3. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-101321A. | |
| Imofinostat | MPT0E028 is an orally active and selective HDAC inhibitor with IC 50 s of 53.0 nM, 106.2 nM, 29.5 nM for HDAC1, HDAC2 and HDAC6, respectively [1]. MPT0E028 reduces the viability of B-cell lymphomas by inducing apoptosis and possesses potent direct Akt targeting ability and reduces Akt phosphorylation in B-cell lymphoma. MPT0E028 has good anticancer activity [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: MPT0E028. CAS No. 1338320-94-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-124295. | |
| IMP-1088 | IMP-1088 is a potent human N-myristoyltransferases NMT1 and NMT2 dual inhibitor with IC50s of <1 nM for HsNMT1 and HsNMT2. IMP-1088 has a Kd of <210 pM for HsNMT1. IMP-1088 efficiently blocks rhinovirus replication by blocking rhinovirus virus-encoded protein (VP0) N-myristoylation. IMP-1088 protects host cells from the cytotoxic effects of viral infection[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2059148-82-0. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-112258. | |
| IMP-1710 | IMP-1710 is a potent and selective deubiquitylating enzyme UCHL1 inhibitor with an IC50 value of 38 nM. IMP-1710 has antifibrotic activity. IMP-1710 is a UCHL1 probe to identify and quantify target proteins in intact human cells[1]. IMP-1710 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. IMP-1710 can be used in the research of idiopathic pulmonary fibrosis[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2383117-96-0. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-138995. | |
| IMP2-IN-1 | IMP2-IN-1 (compound 4) is a potent IMP2 inhibitor with IC50 value of 81.3~127.5 for IMP2 RNA sequence. IMP2-IN-1 reduces IMP2 in SW480 cells. IMP2-IN-1 significantly reduces the viability of both differentiated and non-differentiated Huh7 cells[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1480482-51-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-146178. | |
| Imperatorin | Imperatorin is an effective of NO synthesis inhibitor ( IC 50 =9.2 μmol), which also is a BChE inhibitor ( IC 50 =31.4 μmol). Imperatorin is a weak agonist of TRPV1 with EC 50 of 12.6±3.2 μM. Uses: Scientific research. Group: Natural products. Alternative Names: Ammidin. CAS No. 482-44-0. Pack Sizes: 10 mM * 1 mL; 25 mg; 50 mg; 100 mg. Product ID: HY-N0285. | |
| Importazole | Importazole is a small molecule inhibitor of the nuclear transport receptor importin-&beta. Uses: Scientific research. Group: Signaling pathways. CAS No. 662163-81-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-101091. | |
| IMR-1 | IMR-1 is a novel class of Notch inhibitor targeting the transcriptional activation with an IC 50 of 26 μM. IMR-1 prevents the recruitment of Mastermind-like 1 (Maml1) to the Notch Ternary Complex (NTC) on chromatin, inhibits Notch target gene transcription and dramatically inhibits tumor growth [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 310456-65-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-100431. | |
| IMR-1A | IMR-1A, a acid metabolite of IMR-1, is a Notch inhibitor with an IC 50 of 0.5 μM. IMR-1A has a 50-fold increase in potency with respect to IMR-1. IMR-1 can metabolize in vivo to IMR-1A [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 331862-41-0. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-100431A. | |
| Imrecoxib | Imrecoxib (BAP-909) is a novel and selective cyclooxygenase 2 ( COX-2 ) inhibitor with an IC 50 value of 18 nM, it also inhibits COX1- activity with an IC 50 value of 115 nM. Imrecoxib (BAP-909) has anti-inflammatory effect [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BAP-909. CAS No. 395683-14-4. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-114200. | |
| IMS2186 | IMS2186 is an anti-choroidal neovascularization (CNV) agent that inhibits angiogenesis upstream of VEGF. IMS2186 can arrest cancer cell cycle in G2/M phase, thus exerting anti-proliferation and anti-angiogenesis effects. IMS2186 has no intraocular toxicity and reduces the amount of eye leakage and diseased cells [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1031206-36-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg. Product ID: HY-101990. | |
| Imsidolimab | Imsidolimab (ANB 019) is a high-affinity, humanized monoclonal antibody of anti- IL-36R. Imsidolimab antagonizes IL-36 cytokine signal transduction. Imsidolimab has potential application in generalized pustular psoriasis (GPP) and other inflammatory skin diseases [1] [2]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: ANB 019. CAS No. 2102543-86-0. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99659. | |
| IMT1 | IMT1 is a first-in-class specific and noncompetitive human mitochondrial RNA polymerase (POLRMT) inhibitor. IMT1 causes a conformational change of POLRMT, which blocks substrate binding and transcription in a dose-dependent way in vitro. IMT1 reduces deoxynucleoside triphosphate levels and citric acid cycle intermediates, resulting in a marked depletion of cellular amino acid levels. IMT1 has the potential for mitochondrial transcription disorders related diseases[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2304621-31-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-134539. | |
| IMT1B | IMT1B (LDC203974) is an orally active, noncompetitive and specific allosteric inhibitor of mitochondrial RNA polymerase (POLRMT) and inhibits mitochondrial DNA (mtDNA) expression. IMT1B has anti-tumour effects[1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: LDC203974. CAS No. 2304621-06-3. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-137067. | |
| IN-1130 | IN-1130 is a highly selective transforming growth factor-? type I receptor kinase (ALK5) inhibitor with an IC50 of 5.3 nM for ALK5-mediated Smad3 phosphorylation. IN-1130 inhibits ALK5 phosphorylation of casein (IC50=36 nM) and p38? mitogen-activated protein kinase (IC50=4.3 ?M). IN-1130 suppresses renal fibrosis in obstructive nephropathy and blocks breast cancer lung metastasis[1][2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 868612-83-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-18758. | |
| Inarigivir ammonium | Inarigivir (ORI-9020) ammonium is a dinucleotide antiviral drug that can significantly reduce liver HBV DNA in transgenic mice expressing hepatitis B virus. Inarigivir (ORI-9020) ammonium acts as a RIG-I (Retinoic acid-inducible gene-I) agonist to activate cellular innate immune responses [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ORI-9020 ammonium; SB-9000 ammonium. CAS No. 2172788-92-8. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-101954A. | |
| Inavolisib | Inavolisib (GDC-0077) is a potent, orally active, and selective PI3Kα inhibitor ( IC 50 =0.038 nM). Inavolisib exerts its activity by binding to the ATP binding site of PI3K, thereby inhibiting the phosphorylation of PIP2 to PIP3. Inavolisib is more selective for mutant versus wild-type PI3K&alpha. Inavolisib can be used for the study of breast cancer [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GDC-0077; RG6114. CAS No. 2060571-02-8. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-101562. | |
| Inaxaplin | Inaxaplin (VX-147) is an orally active apolipoprotein L1 ( APOL1 ) function inhibitor (WO2020131807, compound 2). Inaxaplin can be used for the research of kidney disease [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: VX-147. CAS No. 2446816-88-0. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-132820. | |
| Inbakicept | Inbakicept is a dimeric human IL-15 receptor alpha (IL-15 Ra) sushi domain/human IgG1 Fc fusion protein and is an IL-15 superagonist complex. Inbakicept is able to form complex N-803 (Nogapendekin alfa inbakicept) with the IL-15 antibody Nogapendekin alfa in a 1:2 ratio. N-803 mimics the function of IL-15 and amplifies anti-CD20 mAb-mediated NK cell responses and antibody-dependent cellular cytotoxicity (ADCC). N-803 also increases degranulation and IFNγ production in cells [1]. Uses: Scientific research. Group: Inhibitory antibodies. CAS No. 2135939-52-3. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99661. | |
| Incadronic acid | Incadronic acid inhibits growth of Dictyostelium discoideum with an IC 50 of 1.6 μM. Incadronic acid binds the farnesyl diphosphate synthase ( FPPS ) in Leishmania major with the K i of 23 nM. Incadronic acid inhibits the bone resorption and reduces bone loss, that can be used in osteoporosis research. Incadronic acid inhibits the proliferation of cells RAW264.7, PC-3 and MCF-7 with IC 50 of 48 to 228.6 μM [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 124351-85-5. Pack Sizes: 1 mg; 5 mg. Product ID: HY-149149. | |
| INCB054329 | INCB054329 is a potent BET inhibitor. Uses: Scientific research. Group: Signaling pathways. CAS No. 1628607-64-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-112504. | |
| INCB-057643 | INCB-057643 is a novel, orally bioavailable BET inhibitor. Uses: Scientific research. Group: Signaling pathways. CAS No. 1820889-23-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-111485. | |
| INCB086550 | INCB086550 is a potent, oral, small-molecule PD-L1 inhibitor with IC 50s value of 3.1, 4.9 and 1.9 nM for human, cynomolgus, and rat, respectively. INCB086550 promotes the dimerization of cell-surface PD-L1 and induces PD-L1 entry into Golgi vesicles then traffick to the nucleus. INCB086550 can be used for multiple cancers research [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: PD-1/PD-L1-IN-8. CAS No. 2230911-59-6. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-134884. | |
| INCB3344 | INCB3344 is a potent, selective and orally bioavailable CCR2 antagonist with IC50 values of 5.1 nM (hCCR2) and 9.5 nM (mCCR2) in binding antagonism and 3.8 nM (hCCR2) and 7.8 nM (mCCR2) in antagonism of chemotaxis activity. Uses: Scientific research. Group: Signaling pathways. CAS No. 1262238-11-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-50674. | |
| Incensole | Incensole, a 14-membered diterpenoid, is isolated from both essential oils and resins of frankincense. Incensole has shown anti-inflammatory and anti-depression activities due to their ability to activate ion channels in the brain to alleviate anxiety or depression [1]. Uses: Scientific research. Group: Natural products. CAS No. 22419-74-5. Pack Sizes: 5 mg; 10 mg. Product ID: HY-N4097. | |
| Incensole Acetate | Incensole acetate is a main constituent of Boswellia carterii resin , has neuroprotective effects against neuronal damage in traumatic and ischemic head injury. Incensole acetate reduces Aβ25 - 35-triggered apoptosis in hOBNSCs [1]. Uses: Scientific research. Group: Natural products. CAS No. 34701-53-6. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-N4098. | |
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