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Filtered Search Results
Medchemexpress LLC HY-100639 5mg Medchemexpress, Roflumilast N-oxide CAS:292135-78-5 Purity:>98%
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Medchemexpress, HY-100639 5mg Roflumilast N-oxide CAS:292135-78-5 Roflumilast N-oxide is a PDE type 4 inhibitor. 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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Selleck Chemical LLC Pioglitazone HCl S2046-200mg
Pioglitazone HCl (AD-4833 U-72107E) is an inhibitor of cytochrome P450 (CYP)2C8 and CYP3A4 enzymes Pioglitazone HCl inhibits CYP2C8 CYP3A4 and CYP2C9 with Ki of 1 7 M 11 8 M and 32 1 M respectively Pioglitazone HCl is also a selective peroxisome proliferator-activated receptor-gamma (PPAR ) agonist with EC50 of 0 93 M and 0 99 M for human PPAR and mouse PPAR respectively Pioglitazone HCl inhibits mitochondrial iron uptake lipid peroxidation and subsequent ferroptosis
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Biotang Inc Rociletinib, Free Base, > 99%, 10MG, AVL-301;CNX-419;CO-1686. M.W. 555.55. C27H28F3N7O3. CAS#1374640-70-6
Rociletinib, Free Base, > 99%, 10MG, AVL-301;CNX-419;CO-1686. M.W. 555.55. C27H28F3N7O3. CAS#1374640-70-6
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Medchemexpress LLC FR194738 FR BS10MM 1ML SOLN
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MedChemExpress | FR194738 free base | 10 mM * 1 mL in DMSO Solution | HY-100303 10 mM * 1 mL in DMSO | Purity: 99.79% | 204067-45-8 | MW: 439.65
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Medchemexpress LLC HY-50709 50mg , A939572 stearoyl-CoA desaturase (SCD) inhibitor;SCD-inhibitor CAS:1032229-33-6 Purity:98%
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Medchemexpress, HY-50709 50mg A939572 stearoyl-CoA desaturase (SCD) inhibitor;SCD-inhibitor CAS:1032229-33-6 Formula:C20H22ClN3O3 IC50: <4 nM (mSCD1), 37 nM (hSCD1) Purity:98% A939572 is a potent, and orally bioavailable SCD1 inhibitor with IC 50 values of <4 nM and 37 nM for mSCD1 and hSCD1 , respectively. 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 423150-91-8 | Medchem Express | BAY-4931 | 5mg | 788478388 | HY-148352 | MFCD02210727 | 421.84 | C22H16ClN3O4
Ambeed | 5-(Difluoromethyl)-2-fluorobenzonitrile | 100mg | 600846440 | A722620 | 934175-58-3 | MFCD18395398 | 171.122 | C8H4F3N
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Medchemexpress LLC 10-methyl-9-(phenoxycarbonyl) acridinium trifluoromethanesulfonate | 161006-14-0 | MFCD01320487 | 99.4% | 463.43 | C22H16F3NO5S | 5 MG
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10-Methyl-9-(phenoxycarbonyl) acridinium trifluoromethanesulfonate is an acridinium-based chemiluminescent reagent used in chemiluminescent assays for sensitive detection of enzymes, antigens, antibodies, and hormones. It converts to a fluorescent acridone upon oxidation and is supplied in small quantities for research and assay development.
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eMolecules 2411639-80-8 | 3,3-Dimethylindolin-4-amine dihydrochloride | 100mg
Ambeed | 45-Dimethoxyphthalic acid | 100mg | 687211752 | A308737 | 577-68-4 | MFCD08693608 | 226.184 | C10H10O6
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Medchemexpress LLC Mps1-IN-3 hydrochloride | 2989453-29-2 | 98.0% | 574.09 | C26H32ClN7O4S | 10MG
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Mps1-IN-3 hydrochloride is a potent, selective inhibitor of the Mps1 (TTK) kinase for biochemical and cellular research, with an in vitro IC50 of about 50 nM; it has been reported to inhibit glioblastoma cell proliferation and sensitize glioblastoma models to vincristine.
- Potent, selective Mps1 kinase inhibitor (IC50 ~50 nM).
- Reported to inhibit glioblastoma proliferation and sensitize to vincristine.
- High purity suitable for research (approximately 98.0%).
- Molecular weight 574.09 and formula C26H32ClN7O4S.
- Soluble in DMSO at ≥ 20 mg/mL for in vitro use.
- Stored sealed at -20°C; solutions stable at -80°C for long term.
- Supplied as a solid in small research sizes.
- Datasheet, SDS, certificate of analysis, and spectral data available.
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Medchemexpress LLC Pnd-1186 hydrochloride | 1356154-94-3 | 99.9% | 537.96 | 100 MG
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PND-1186 hydrochloride (VS-4718 hydrochloride) is a potent, highly-specific, and reversible inhibitor of FAK (Focal Adhesion Kinase) with an IC50 of 1.5 nM. This compound has demonstrated the ability to selectively promote tumor cell apoptosis. It is intended for research use only.
- Potent, highly-specific, and reversible fak inhibitor.
- Selectively promotes tumor cell apoptosis.
- Effective in inhibiting fak Tyr-397 phosphorylation in breast carcinoma cells.
- Shown to inhibit 4t1 subcutaneous tumor growth in animal models by inducing apoptosis.
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Medchemexpress LLC HY-10809 5mg Medchemexpress, Bitopertin CAS:845614-11-1 Purity:>98%
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Medchemexpress, HY-10809 5mg Bitopertin CAS:845614-11-1 Bitopertin is a potent, noncompetitive glycine reuptake inhibitor, inhibits glycine uptake at human GlyT1 with a concentration exhibiting IC50 of 25 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 MCOPPB trihydrochloride | 1108147-88-1 | 99.98% | 100 MG
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MCOPPB trihydrochloride is a nociceptin receptor agonist with a pKi of 10.07, demonstrating weaker activity at other opioid receptors. It is the trihydrochloride form of MCOPPB, which is described as a new nonpeptide nociceptin/orphanin FQ peptide (NOP)-receptor agonist. It has a pKi of 10.07 ± 0.01 for the human NOP receptor. This product is for research use only.
- Nociceptin receptor agonist
- Weaker activity at other opioid receptors
- Nonpeptide nociceptin/orphanin FQ peptide (NOP)-receptor agonist
- For research use only
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Medchemexpress LLC S -VERAPAMIL HYDRO 50 mg
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S -VERAPAMIL HYDRO 50MG
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Medchemexpress LLC P38A INHIBITOR 2 100 mg
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P38A INHIBITOR 2 100MG
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eMolecules EMOLECULES INC
5000471999 2 6-DIMETHOXYBENZENE-1-SUL 10G
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