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Filtered Search Results
eMolecules 223749-46-0 | Medchem Express | HMR 1556 | 5mg | 482203866 | HY-106369 | MFCD12756323 | 411.44 | C17H24F3NO5S
Medchem Express | Gelsemine | 5mg | 441682058 | HY-N0388 | 509-15-9 | 322.408 | C20H22N2O2
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Accela Chembio Inc Bis(pentafluorophenyl) Carbonate | 25g | 59483-84-0 | MFCD00368353 | 97+% | Shelf Life: 1440 Days | +4
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Bis(pentafluorophenyl) Carbonate | 25g | 59483-84-0 | MFCD00368353 | 97+% | Shelf Life: 1440 Days | +4
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Medchemexpress LLC Tucatinib hemiethanolate | 1429755-56-5 | 98.8% | 503.57 | 100 MG
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Tucatinib hemiethanolate is a potent, orally active, and selective HER2 inhibitor. With an IC50 of 8 nM, it selectively targets HER2, showing approximately 500-fold selectivity over EGFR in cell-based assays. This compound is intended for research use only.
- Potent, orally active, and selective HER2 inhibitor
- Selectively inhibits receptor tyrosine kinase HER2 relative to EGFR
- Blocks proliferation and phosphorylation of HER2 and its downstream effector Akt
- Demonstrated anti-tumor activity and improved survival in animal models
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Medchemexpress LLC AMTB hydrochloride | 926023-82-7 | 99.2% | 430.99 | C23H27ClN2O2S | 5 MG
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AMTB hydrochloride is a research-grade small molecule that selectively blocks TRPM8 ion channels and also inhibits voltage-gated sodium channels. Supplied as a white to off-white solid with high chemical purity, it is intended for in-vitro and in-vivo research applications investigating TRPM8-mediated physiology and pharmacology.
- Selective TRPM8 channel blocker and non-selective voltage-gated sodium channel inhibitor.
- High purity: 99.18%.
- White to off-white solid form suitable for formulation.
- Soluble in DMSO (up to 100 mg/mL) with sonication.
- In vivo formulation protocols available for concentrations ≥ 2.5 mg/mL.
- Supplied in small research pack sizes, including 5 mg.
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eMolecules 63019-39-6 | 3-Hydroxychrysene | Toronto Research Chemicals | MFCD01736446 | 244.293 | C18H12OOc1ccc2ccc3c4ccccc4ccc3c2c1 | 100mg | 483412499
3-Hydroxychrysene | Toronto Research Chemicals | 63019-39-6 | MFCD01736446 | 244.293 | C18H12OOc1ccc2ccc3c4ccccc4ccc3c2c1 | 100mg | 483412499
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Medchemexpress LLC Arn-21934 | 2230854-93-8 | 98.1% | 360.46 | 100 MG
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ARN-21934 is a potent, highly selective, and blood-brain barrier (BBB) penetrant inhibitor specifically targeting human topoisomerase II α over β. It inhibits DNA relaxation with an IC50 of 2 μM, making it significantly more potent than the anticancer agent Etoposide. ARN-21934 demonstrates a favorable in vivo pharmacokinetic profile and is considered a promising lead compound for anticancer research.
- High potency and selectivity: Potently and selectively inhibits human topoisomerase II α.
- Blood-brain barrier penetrant: Able to cross the blood-brain barrier.
- Favorable pharmacokinetic profile: Exhibits good clearance values and a half-life of 149 minutes in circulation.
- Anticancer potential: Shows antiproliferation activity against various human cancer cell lines.
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Medchemexpress LLC 5-O-Methylvisammioside | 84272-85-5 | 452.45 | 50 MG
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5-O-Methylvisammioside is a natural compound isolated from Saposhnikovia divaricata.
- Natural compound
- Isolated from Saposhnikovia divaricata
- Purity: 99.90%
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Medchemexpress LLC HY-18706 10mg Medchemexpress, Tranilast (trans-) CAS:70806-55-2 Purity:>98%
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Medchemexpress, HY-18706 10mg Tranilast (trans-) CAS:70806-55-2 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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eMolecules 79714-31-1 | Medchem Express | Risarestat | 5mg | 415687763 | HY-16433 | MFCD01940023 | 323.41 | C16H21NO4S
Medchem Express | Risarestat | 5mg | 415687763 | HY-16433 | 79714-31-1 | MFCD01940023 | 323.410 | C16H21NO4S
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Medchemexpress LLC LY367385 hydrochloride | 2829282-00-8 | 99.4% | 245.66 g·mol⁻¹ | C10H12ClNO4 | 5 MG
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LY367385 hydrochloride is a selective metabotropic glutamate receptor 1a (mGluR1a) antagonist used as a research reagent in neuropharmacology. It inhibits quisqualate-induced phosphoinositide hydrolysis (IC50 = 8.8 μM) and is provided as a solid for in vitro and formulation studies.
- High purity: 99.44%.
- Molecular weight: 245.66 g·mol⁻¹.
- CAS number: 2829282-00-8.
- Soluble in DMSO (125 mg/mL) and water (12.5 mg/mL) with ultrasonic aid.
- In vivo formulation protocols produce clear solutions ≥2.08 mg/mL in common vehicles.
- Storage: solid at 4°C; stock solutions at -80°C (6 months) or -20°C (1 month).
- Available in small-scale packages suitable for research, including 5 mg.
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eMolecules 173392-87-5 | 4-(N-Nonyloxy)phenylboronic acid | Combi-Blocks | MFCD04039033 | 264.170 | C15H25BO3 | 98.000 | CCCCCCCCCOc1ccc(cc1)B(O)O | 1g | 117526339
4-(N-Nonyloxy)phenylboronic acid | Combi-Blocks | 173392-87-5 | MFCD04039033 | 264.170 | C15H25BO3 | 98.000 | CCCCCCCCCOc1ccc(cc1)B(O)O | 1g | 117526339
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Medchemexpress LLC Dapoxetine-d7 hydrochloride | 2699607-47-9 | 100.0% | 1 MG
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Dapoxetine-d7 hydrochloride is the deuterium labeled form of Dapoxetine hydrochloride, a short-acting selective serotonin reuptake inhibitor (SSRI). This compound is intended for research use only.
- Utilized as a tracer
- Serves as an internal standard for quantitative analysis through techniques such as NMR, GC-MS, or LC-MS
- Short-acting selective serotonin reuptake inhibitor (SSRI)
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Sigma Aldrich Fine Chemicals Biosciences Neostigmine methyl sulfate | 51-60-5 | MFCD00011796 | 5G
Neostigmine methyl sulfate | Mol Wt: 334.39 | 51-60-5 | MFCD00011796 | 5G
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Medchemexpress LLC HG-7-85-01-NH2 | 1258391-29-5 | 98.1% | 50 MG
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HG-7-85-01-NH2 is a small-molecule ligand derived from an ABL inhibitor. It serves as a target protein ligand for synthesizing the heterobifunctional molecule SNIPER and can bind to an IAP ligand via a linker to form SNIPER(ABL)-033. The resulting SNIPER(ABL)-033 effectively degrades BCR-ABL protein.
- Derived from an ABL inhibitor.
- Functions as a target protein ligand for SNIPER synthesis.
- Forms a heterobifunctional molecule when linked to an IAP ligand.
- Used in the formation of SNIPER(ABL)-033, which degrades BCR-ABL protein.
- Intended for research use only.
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Medchemexpress LLC Trifarotene | 895542-09-3 | 99.1% | 459.58 g/mol | C29H33NO4 | 100 MG
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Trifarotene is a selective retinoic acid receptor γ (RARγ) agonist supplied as a white to off-white solid for research use. It is intended for in vitro and in vivo studies of RAR/RXR signaling and related pathways and is not for human therapeutic use.
- High purity (≈99.1% by LCMS)
- Chemical formula C29H33NO4, molecular weight 459.58 g/mol
- Soluble in DMSO (≈250 mg/mL) and formulatable for in vivo dosing
- Stable under recommended powder and solution storage conditions
- Suitable for receptor pharmacology and preclinical studies
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