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Filtered Search Results
![eMolecules 100286-90-6 | IRINOTECAN HCL | AstaTech | MFCD01862255 | 623.150 | C33H39ClN4O6 | 98.000 | Cl.CCc1c2Cn3c(cc4c(COC(=O)[C@]4(O)CC)c3=O)-c2nc2ccc(OC(=O)N3CCC(CC3)N3CCCCC3)cc12 | 1g | 248482741](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502170691.JPG-250.jpg)
eMolecules 100286-90-6 | IRINOTECAN HCL | AstaTech | MFCD01862255 | 623.150 | C33H39ClN4O6 | 98.000 | Cl.CCc1c2Cn3c(cc4c(COC(=O)[C@]4(O)CC)c3=O)-c2nc2ccc(OC(=O)N3CCC(CC3)N3CCCCC3)cc12 | 1g | 248482741
IRINOTECAN HCL | AstaTech | 100286-90-6 | MFCD01862255 | 623.150 | C33H39ClN4O6 | 98.000 | Cl.CCc1c2Cn3c(cc4c(COC(=O)[C@]4(O)CC)c3=O)-c2nc2ccc(OC(=O)N3CCC(CC3)N3CCCCC3)cc12 | 1g | 248482741
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![eMolecules 1184-89-0 | Dibromochloronitromethane | Toronto Research Chemicals | MFCD11040919 | 253.270 | CBr2ClNO2[O-][N+](=O)C(Cl)(Br)Br | 100mg | 601593601](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502176078.JPG-250.jpg)
eMolecules 1184-89-0 | Dibromochloronitromethane | Toronto Research Chemicals | MFCD11040919 | 253.270 | CBr2ClNO2[O-][N+](=O)C(Cl)(Br)Br | 100mg | 601593601
Dibromochloronitromethane | Toronto Research Chemicals | 1184-89-0 | MFCD11040919 | 253.270 | CBr2ClNO2[O-][N+](=O)C(Cl)(Br)Br | 100mg | 601593601
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Medchemexpress LLC Eliglustat-d4 | 98.0% | 408.57 | 5 MG
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Eliglustat-d4 is the deuterium labeled Eliglustat. Eliglustat is a specific, potent, and orally active glucocerebroside synthase inhibitor with an IC50 of 24 nM. Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs.
- It is the deuterium labeled version of Eliglustat.
- It can be used as a tracer.
- It can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
- Deuteration has potential to affect the pharmacokinetic and metabolic profiles of drugs.
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Accela Chembio Inc Bis(pentafluorophenyl) Carbonate | 5g | 59483-84-0 | MFCD00368353 | 97+% | Shelf Life: 1440 Days | +4
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Bis(pentafluorophenyl) Carbonate | 5g | 59483-84-0 | MFCD00368353 | 97+% | Shelf Life: 1440 Days | +4
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Medchemexpress LLC ITX5061 | 1252679-52-9 | 99.7% | 620.16 | 50 MG
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ITX5061 is a type II inhibitor of p38 MAPK and an antagonist of scavenger receptor B1 (SR-B1). It is for research use only and not sold to patients.
- Inhibitor type: type II inhibitor of p38 MAPK and antagonist of scavenger receptor B1 (SR-B1).
- Biological activity (in vitro): inhibits mouse SR-B1 overexpressed in CHO cells with an IC50 of 0.77 μM.
- Biological activity (in vivo): increases HDL-C levels and decreases HDL-CE catabolism in mice.
- Appearance: solid.
- Color: light yellow to light brown.
- Shipping: room temperature in continental US; may vary elsewhere.
- Storage: 4°C, sealed storage, away from moisture. In solvent: -80°C for 6 months; -20°C for 1 month.
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eMolecules 632-79-1 | Tetrabromophthalic anhydride | Oakwood Chemicals | MFCD00005919 | 463.701 | C8Br4O3 | 95.000 | Brc1c2C(=O)OC(=O)c2c(Br)c(Br)c1Br | 25g | 480169571
Tetrabromophthalic anhydride | Oakwood Chemicals | 632-79-1 | MFCD00005919 | 463.701 | C8Br4O3 | 95.000 | Brc1c2C(=O)OC(=O)c2c(Br)c(Br)c1Br | 25g | 480169571
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Medchemexpress LLC HY-102014 5mg Medchemexpress, RN-18 CAS:431980-38-0 Purity:>98%
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Medchemexpress, HY-102014 5mg RN-18 CAS:431980-38-0 RN-18 is a HIV-1 viral infectivity factor (HIV-1 Vif) inhibitor with an IC50 of 6 μM in nonpermissive H9 cells. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC HY-10202A 50mg Medchemexpress, Tandutinib (hydrochloride) CAS: Purity:>98%
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Medchemexpress, HY-10202A 50mg Tandutinib (HCl) CAS: Tandutinib hydrochloride (MLN518 hydrochloride) is a potent and selective inhibitor of the FLT3 with an IC50 of 0.22 μM, and also inhibits c-Kit and PDGFR with IC50s of 0.17 μM and 0.20 μM, respectively. Tandutinib hydrochloride can be used for acute myelogenous leukemia (AML). Tandutinib hydrochloride has the ability to cross the blood-brain barrier[3]. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC HY-103533 5mg Medchemexpress, Gabazine CAS:104104-50-9 Purity:>98%
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Medchemexpress, HY-103533 5mg Gabazine CAS:104104-50-9 Gabazine is a selective and competitive antagonist of GABAA receptor, with an IC50 of ~0.2 μM for GABA receptor. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC Apabetalone | 1044870-39-4 | 99.34% | 370.40 | 100 MG
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Apabetalone (RVX-208) is an inhibitor of BET transcriptional regulators, specifically targeting the second bromodomain (BD2) with high selectivity. It enhances the production of ApoA-I in hepatocytes, leading to an increase in high-density lipoprotein cholesterol (HDL-C). Its mechanism involves binding to bromodomains of the BET family by competing for acetylated lysine binding sites. This epigenetic modulation of ApoA-I production suggests it as a potential therapeutic agent for atherosclerosis.
- Selective BET transcriptional regulator inhibitor
- Targets the second bromodomain (BD2)
- Increases ApoA-I production in liver cells
- Elevates high-density lipoprotein cholesterol (HDL-C)
- Acts via an epigenetic mechanism
- Investigated for atherosclerosis treatment
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Medchemexpress LLC Sb-3Ct 10 Mm 1 Ml In Dmso | HY-12354
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Sb-3Ct 10 Mm 1 Ml In Dmso
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Medchemexpress LLC Ibrutinib-mpea | 1710768-30-1 | MFCD31813735 | 99.7% | 581.71 | C32H39N9O2 | 10 MG
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Ibrutinib-MPEA is a synthetic derivative of ibrutinib used as a research reagent to probe Bruton's tyrosine kinase (BTK) biology and structure-activity relationships. It is supplied as a high-purity solid suitable for biochemical and cellular assay applications.
- High purity: 99.7%.
- Molecular weight: 581.71 g/mol.
- Molecular formula: C32H39N9O2.
- Supplied as a 10 mg vial for laboratory use.
- For research use only; not for human or veterinary applications.
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Medchemexpress LLC HY-12381 5mg Medchemexpress, ML224 CAS:1338824-21-7 Purity:>98%
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Medchemexpress, HY-12381 5mg ML224 CAS:1338824-21-7 Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC HY-16500 5mg Medchemexpress, Tolrestat CAS:82964-04-3 Purity:>98%
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Medchemexpress, HY-16500 5mg Tolrestat CAS:82964-04-3 Tolrestat is a potent, orally active aldose reductase inhibitor with IC50 of 35 nM. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC S-verapamil hydrochloride | 36622-28-3 | MFCD11045898 | 98.3% | C27H39ClN2O4 | 10MG
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(S)-Verapamil hydrochloride is the S-enantiomer of the calcium channel blocker verapamil, supplied as the hydrochloride salt for use in pharmacology and transporter research. It is reported to inhibit leukotriene C4 (LTC4) and calcein transport by the multidrug resistance protein MRP1 and is provided as a high-purity research reagent.
- Enantiomer-specific activity useful for stereoselective studies.
- Suitable for transporter and pharmacology assays.
- Hydrochloride salt form improves solubility in polar solvents.
- Reported inhibition of LTC4 and MRP1-mediated transport.
- High purity (98.3%) for reproducible experimental results.
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