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Filtered Search Results
Sigma Aldrich 2-Isopropylphenol
MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.
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| Boiling Point | 212°C to 213°C (lit.) |
|---|---|
| Percent Purity | 98% |
| Linear Formula | (CH3)2 CHC6H4OH |
| CAS | 88-69-7 |
| Molecular Weight (g/mol) | 136.19 |
| MDL Number | MFCD00002224 |
| Refractive Index | n20/D 1.526 (literature) |
| RTECS Number | SL5900000 |
| Recommended Storage | Room Temperature |
| Molecular Formula | C9H12O |
| EINECS Number | 201-852-8 |
| Density | 1.012 g/mL (at 25°C (literature)) |
| Melting Point | 12°C to 16°C (lit.) |
Sigma Aldrich 3-Chloro-4-(trifluoromethylthio)aniline
MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.
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| CAS | 64628-74-6 |
|---|
Medchemexpress LLC ML-193 | 713121-80-3 | 99.7% | 527.59 | 1 ML
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ML-193 (CID 1261822) is a potent and selective antagonist of GPR55, demonstrating more than 27-fold selectivity for GPR55 over GPR35, CB1, and CB2. It has been shown to improve motor and sensorimotor deficits in Parkinson's disease (PD) rat models.
- Inhibits β-arrestin trafficking induced by L-α-lysophosphatidylinositol and ML186.
- Decreases LPI-mediated ERK1/2 phosphorylation in U2OS cells.
- Attenuates GPR55 agonists induced increases in hNSCs proliferation rates.
- Attenuates ML184-induced increases in hNSCs differentiation.
- Attenuates sensorimotor deficits and slip steps in Parkinson's disease rat models.
- Increases motor coordination in Parkinson's disease rat models.
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Chem-Impex International, Inc. 2,4,6-Triisopropylbenzenesulfonyl chloride | MFCD00007433 | 100G
2,4,6-Triisopropylbenzenesulfonyl chloride, MFCD00007433, 100G
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Chem-Impex International, Inc. 1,3-Bis(2,6-diisopropylphenyl)imidazolinium chloride | MFCD07369796 | 5G
1,3-Bis(2,6-diisopropylphenyl)imidazolinium chloride, MFCD07369796, 5G
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Medchemexpress LLC Foropafant | 136468-36-5 | 100.0% | 100 MG
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Foropafant is a highly potent, competitive, selective, and orally active antagonist of the platelet-activating factor (PAF) receptor. It is characterized by a Ki value of 57 pM for [3H]PAF binding, which is significantly lower than unlabeled PAF, and effectively inhibits PAF-induced aggregation in both rabbit and human platelets. This product is intended for research use only and should be handled by qualified personnel.
- Highly potent and selective PAF receptor antagonist
- Orally active compound
- Inhibits PAF-induced platelet aggregation
- Suitable for various research applications
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Medchemexpress LLC Az194 | 2241651-99-8 | 99.8% | 567.63 | C34H31F2N3O3 | 5 MG
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AZ194 is a research small-molecule inhibitor of the CRMP2-Ubc9 interaction and the NaV1.7 sodium channel (IC50 = 1.2 μM). It blocks SUMOylation of CRMP2 and selectively reduces NaV1.7 surface expression, producing antinociceptive effects in preclinical pain models. Supplied as a white to off-white solid for laboratory research use.
- Inhibits CRMP2-Ubc9 interaction and NaV1.7 (IC50 = 1.2 μM).
- Molecular weight: 567.63 g/mol.
- Chemical formula: C34H31F2N3O3.
- High purity (>99.8%) suitable for research applications.
- Appearance: white to off-white solid.
- Soluble in DMSO at approximately 33.33 mg/mL; may require ultrasonic assistance.
- Storage recommendations: powder at -20°C or 4°C; aliquot solutions and store at -80°C.
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eMolecules 51202-00-7 | 2-Chloro-4-isopropylphenol | MFCD16997172 | 1g
Ambeed | 2-Chloro-4-isopropylphenol | 1g | 602849145 | A1136688 | 51202-00-7 | MFCD16997172 | 170.640 | C9H11ClO
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eMolecules 1253643-88-7 | Medchem Express | DiAzKs | 5mg | 587658734 | HY-D0853 | MFCD28133397 | 272.305 | C11H20N4O4
AstaTech | (3-FLUORO-4-(4-METHYLPIPERAZIN-1-YL)PHENYL)BORONIC ACID PINACOL ESTER | 0.25g | 273174405 | 77012 | 95.000 | 1408088-34-5 | MFCD22988988 | 320.220 | C17H26BFN2O2
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Medchemexpress LLC HY-14463 10mg Medchemexpress, Onalespib CAS:912999-49-6 Purity:>98%
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Medchemexpress, HY-14463 10mg Onalespib CAS:912999-49-6 Onalespib (AT13387) is a long-acting second-generation Hsp90 inhibitor with a Kd of 0.71 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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eMolecules 1110781-88-8 | Medchem Express | Ro 5212773 | 5mg | 680109508 | HY-110098 | MFCD21605509 | 378.395 | C20H21F3N2O2
Ambeed | (5-Formyl-2-methylphenyl)boronic acid | 100mg | 718039769 | A401980 | 1186398-35-5 | MFCD16295249 | 163.970 | C8H9BO3
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eMolecules 81090-34-8 | 4-Bromo-2-isopropylaniline | Oakwood Chemical | MFCD11845955 | 214.106 | C9H12BrN | 94.000 | CC(C)c1cc(Br)ccc1N | 1g | 537688227
4-Bromo-2-isopropylaniline | Oakwood Chemical | 81090-34-8 | MFCD11845955 | 214.106 | C9H12BrN | 94.000 | CC(C)c1cc(Br)ccc1N | 1g | 537688227
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Medchemexpress LLC HY-33353 10mg Medchemexpress, GSK-4716 CAS:101574-65-6 Purity:>98%
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Medchemexpress, HY-33353 10mg GSK-4716 CAS:101574-65-6 GSK-4716 is a selective ERRβ/γ agonist. 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 1572414-83-5 | Medchem Express | ML-323 | 5mg | 446268600 | HY-17543 | MFCD28099817 | 384.487 | C23H24N6
Medchem Express | KNK437 | 5mg | 446254960 | HY-100110 | 218924-25-5 | MFCD24369049 | 245.234 | C13H11NO4
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Medchemexpress LLC Brite-338733 | 503105-88-2 | 98.9% | 433.59 | 10 MG
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BRITE-338733 is an inhibitor of E. coli RecA ATPase activity (IC50: 4.7 μM). It also inhibits the ATP hydrolysis activity of RSC chromatin remodeling enzyme by binding to its ATP-binding pocket and DNA (IC50: 0.316 μM). BRITE-338733 exhibits cytotoxicity against MCF-7 and MDA-MB-231 breast cancer cells. It can be used in studies on antibacterial adjuvants and anticancer research.
- Exhibits strong and stable binding affinity for the ATPase domain of Sth1, the catalytic subunit of the yeast RSC complex.
- Potently inhibits the ATP hydrolysis activity of purified yeast RSC complex.
- Exhibits cytotoxicity against human breast cancer cell lines MCF-7 and MDA-MB-231.
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