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Filtered Search Results
eMolecules 860624-90-4 | 5-Bromo-1H-indole-7-carboxylic acid | Ambeed | MFCD11845481 | 240.056 | C9H6BrNO2 | 97.000 | OC(=O)c1cc(Br)cc2cc[nH]c12 | 1g | 525163768
5-Bromo-1H-indole-7-carboxylic acid | Ambeed | 860624-90-4 | MFCD11845481 | 240.056 | C9H6BrNO2 | 97.000 | OC(=O)c1cc(Br)cc2cc[nH]c12 | 1g | 525163768
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Aobchem 5-Chloro-1H-indole | ≥95% | CAS 17422-32-1 | C8H6ClN | 25g
5-Chloro-1H-indole | ≥95% | CAS 17422-32-1 | C8H6ClN | 25g
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Aobchem 4-Bromo-7-isopropyl-1H-indole | 97% | CAS 1219741-52-2 | C11H12BrN | 500mg
4-Bromo-7-isopropyl-1H-indole | 97% | CAS 1219741-52-2 | C11H12BrN | 500mg
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Aobchem Methyl 1H-indole-5-carboxylate | ≥97% | CAS 1011-65-0 | C10H9NO2 | 10g
Methyl 1H-indole-5-carboxylate | ≥97% | CAS 1011-65-0 | C10H9NO2 | 10g
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eMolecules 3764-94-1 | 5-Chlorotryptamine hydrochloride | Chem-Impex | MFCD00130168 | 194.660 | C10H11ClN2 | 95.000 | NCCc1c[nH]c2ccc(Cl)cc12 | 1g | 112755555
5-Chlorotryptamine hydrochloride | Chem-Impex | 3764-94-1 | MFCD00130168 | 194.660 | C10H11ClN2 | 95.000 | NCCc1c[nH]c2ccc(Cl)cc12 | 1g | 112755555
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Medchemexpress LLC Nevadensin | 10176-66-6 | 344.32 | 5 MG
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Nevadensin (Lysionotin) is a natural flavonoid that acts as a selective human carboxylesterase 1 (hCE1) inhibitor with an IC50 of 2.64 μM, showing more selectivity for hCE1 than hCE2 (IC50 of 132.8 μM). It can induce apoptosis and DNA damage in cancer cells. This compound exhibits a range of pharmacological effects, including anti-inflammatory, anti-tumour, anti-hypertensive, anti-tubercular, antitussive, antioxidant, and anti-microbial activities.
- Natural flavonoid
- Selective human carboxylesterase 1 (hCE1) inhibitor
- Induces apoptosis and DNA damage in cancer cells
- Possesses anti-inflammatory activity
- Exhibits anti-tumour effects
- Has anti-hypertensive properties
- Demonstrates anti-tubercular activity
- Acts as an antitussive
- Functions as an antioxidant
- Shows anti-microbial activities
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Medchemexpress LLC Erenapurstat | 136164-66-4 | 99.67% | 378.46 | 50 MG
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Erenapurstat (E3330) is a direct, orally active and selective inhibitor of Ape-1 (apurinic/apyrimidinic endonuclease 1)/Ref-1 (redox factor-1) redox. It impairs tumor growth and blocks the activity of NF-κB, AP-1, and HIF-1α in pancreatic cancer, showing anticancer activities.
- Targets Ape-1 and Ref-1
- Inhibits growth of HUVECs, PCECs, and EPCs
- Reduces VEGF expression in pancreatic cancer cells
- Inhibits differentiation of BM-MSCs into CD31+ endothelial lineage cells
- Decreases cell viability in H1975 cells
- Inhibits growth and migration of pancreatic cancer cells
- Enhances intracellular ROS level and inhibits CD44 expression in PANC1 cells
- Neuroprotective against cisplatin-induced alterations
- Attenuates liver injury in rats
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eMolecules 850623-66-4 | Potassium trifluoro(4-isobutylphenyl)borate | Ambeed | MFCD04115761 | 240.120 | C10H13BF3K | 98.000 | [K+].CC(C)Cc1ccc(cc1)[B-](F)(F)F | 1g | 586036590
Potassium trifluoro(4-isobutylphenyl)borate | Ambeed | 850623-66-4 | MFCD04115761 | 240.120 | C10H13BF3K | 98.000 | [K+].CC(C)Cc1ccc(cc1)[B-](F)(F)F | 1g | 586036590
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Sigma Aldrich Fine Chemicals Biosciences 5-Benzyloxytryptamine hydrochloride 98% | 52055-23-9 | MFCD00012685 | 1G
5-Benzyloxytryptamine hydrochloride 98% | Purity: 98% | Mol Wt: 302.8 | 52055-23-9 | MFCD00012685 | 1G
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Medchemexpress LLC Sisunatovir hydrochloride | 1903763-83-6 | 98.6% | 482.90 g/mol | C23H23ClF4N4O | 5MG
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Sisunatovir hydrochloride is the hydrochloride salt of sisunatovir (RV521), an orally active respiratory syncytial virus (RSV) fusion protein inhibitor supplied as a research-grade solid for in vitro and in vivo antiviral studies. It has defined molecular properties and high analytical purity appropriate for pharmacology and virology research.
- Potent RSV fusion inhibitor for antiviral research.
- Provided as a hydrochloride salt in solid powder form.
- High purity suitable for in vitro and in vivo studies.
- Well characterized molecular weight and chemical formula.
- Available in small research-scale quantities for assay use.
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eMolecules 857969-66-5 | 5-Bromothiazolo[5,4-b]pyridine | ChemScene | MFCD17014628 | 215.070 | C6H3BrN2S | 97.000 | Brc1ccc2ncsc2n1 | 100mg | 632303341
5-Bromothiazolo[5,4-b]pyridine | ChemScene | 857969-66-5 | MFCD17014628 | 215.070 | C6H3BrN2S | 97.000 | Brc1ccc2ncsc2n1 | 100mg | 632303341
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eMolecules 1227374-66-4 | Ambeed | (11bR)-N-(26-Di(naphthalen-1-yl)-4-oxido-89101112131415-octahydrodinaphtho[21-d12-f][132]dioxaphosphepin-4-yl)-111-trifluoromethanesulfonamide | 50mg | 633658969 | A1006129 | 739.75 | C41H33F3NO5PS
Ambeed | 1-(Chloro(pyrrolidin-1-yl)methylene)pyrrolidin-1-ium hexafluorophosphate(V) | 5g | 600846473 | A723618 | 135540-11-3 | MFCD00191333 | 332.660 | C9H16ClF6N2P
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Medchemexpress LLC Farudodstat (ASLAN003) | 1035688-66-4 | 99.7% | 100 MG
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Farudodstat (ASLAN003) is an orally active and potent Dihydroorotate Dehydrogenase (DHODH) inhibitor with an IC50 of 35 nM for the human DHODH enzyme. Its mechanism of action involves inhibiting protein synthesis by activating AP-1 transcription factors. This compound induces apoptosis and significantly prolongs survival in acute myeloid leukemia (AML) xenograft mice.
- Exhibits antiproliferative activity against various human cell lines.
- Inhibits leukemic cell proliferation in vitro.
- Increases cleaved caspase 8.
- Decreases viability and induces differentiation in primary acute myeloid leukemia blasts and myelodysplastic syndrome samples.
- Inhibits protein synthesis by reducing O-propargyl-puromycin (OPP) incorporation and downregulating EIF4B and RPL6 proteins.
- Substantially reduces the number and size of disseminated tumors in vivo.
- Available as a white to off-white solid.
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Medchemexpress LLC Maralixibat chloride | 228113-66-4 | 99.6% | 710.41 | 5 MG
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Maralixibat chloride (SHP625) is an orally active ileal bile acid transporter (IBAT) inhibitor. It is used for the research of rare cholestatic liver diseases including Alagille syndrome (ALGS), progressive familial intrahepatic cholestasis (PFIC), and biliary atresia. It reduces elevations in sBA levels, improves liver function, and reduces liver tissue damage in cholestasis models.
- Orally active ileal bile acid transporter (IBAT) inhibitor
- Suitable for research into rare cholestatic liver diseases such as Alagille syndrome, progressive familial intrahepatic cholestasis, and biliary atresia
- Reduces elevations in sBA levels
- Improves liver function
- Reduces liver tissue damage in cholestasis models
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eMolecules 191403-66-4 | (S)-1-BENZYL-4-HYDROXY-2-PYRROLIDINONE | AstaTech | MFCD00672872 | 191.230 | C11H13NO2 | 97.000 | O[C@@H]1CN(Cc2ccccc2)C(=O)C1 | 0.25g | 200610938
(S)-1-BENZYL-4-HYDROXY-2-PYRROLIDINONE | AstaTech | 191403-66-4 | MFCD00672872 | 191.230 | C11H13NO2 | 97.000 | O[C@@H]1CN(Cc2ccccc2)C(=O)C1 | 0.25g | 200610938
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