Cell Culture Media, Supplements, and Reagents
Medchemexpress LLC Cdk9-in-13 | 2768712-71-4 | 99.94% | 461.60 | 100 MG
CDK9-IN-13 (compound 38) is a potent and selective CDK9 inhibitor, with an IC50 of <3 nM. It exhibits short half-lives in rodents. It is suitable for laboratory centrifugation and storage.
- Potent and selective cdk9 inhibitor
- Ic50 of <3 nm
- Short half-lives in rodents
- Cdk1: 0.14 μm
- Cdk2: 0.72 μm
- Cdk7: 0.40 μm
- Cdk12: 0.055 μm
Medchemexpress LLC CDK9-IN-13 | 2768712-71-4 | 99.9% | 461.60 | 50 MG
CDK9-IN-13 is a potent and selective CDK9 inhibitor, demonstrating an IC50 of <3 nM. It also shows inhibitory activity against CDK1, CDK2, CDK7, and CDK12. The compound exhibits short half-lives in rodents and is intended for research use only.
- Potent and selective CDK9 inhibitor
- Inhibits CDK1, CDK2, CDK7, and CDK12
- Suitable for research use only
- Short half-lives in rodents
- Store powder at -20°C for 3 years or 4°C for 2 years
- Store in solvent at -80°C for 6 months or -20°C for 1 month
- Soluble in DMSO (2.5 mg/mL)
Medchemexpress LLC HY-100022 1mg Medchemexpress, Tomivosertib CAS:1849590-01-7 Purity:>98%
Medchemexpress, HY-100022 1mg Tomivosertib CAS:1849590-01-7 Tomivosertib (eFT508) is a potent, highly selective, and orally active MNK1 and MNK2 inhibitor, with IC50s of 1-2 nM against both isoforms. Tomivosertib (eFT508) treatment leads to a dose-dependent reduction in eIF4E phosphorylation at serine 209 (IC50=2-16 nM) in tumor cell lines. Tomivosertib (eFT508) also dramatically downregulates PD-L1 protein abundance[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.
Sigma Aldrich Fine Chemicals Biosciences 4-Hexylresorcinol analytical standard | 136-77-6 | MFCD00002284 | 25MG
4-Hexylresorcinol analytical standard | Purity: >=98.0% (GC) | Mol Wt: 194.27 | 136-77-6 | MFCD00002284 | 25MG
Selleck Chemical LLC Clomipramine HCl 50mg 17321-77-6
Clomipramine HCl is a hydrochloride salt of clomipramine which is a serotonin transporter (SERT), norepinephrine transporter (NET) dopamine transporter (DAT) blocker with Ki of 0.14, 54 and 3 nM, respectively. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
Medchemexpress LLC HPK1-IN-7 | 2320462-65-3 | 99.33% | 458.47 | 100 MG
HPK1-IN-7 is a potent, orally active hematopoietic progenitor kinase 1 inhibitor with excellent family and kinome selectivity. It demonstrates robust efficacy in tumor models in combination with anti-PD1.
- Potent and selective inhibitor
- Orally active
- Shows selectivity against IRAK4 and GLK
- Enhances anti-PD1 efficacy in syngeneic tumor models
Medchemexpress LLC HY-100463 10mg Medchemexpress, TPI-1 CAS:79756-69-7 Purity:>98%
Medchemexpress, HY-100463 10mg TPI-1 CAS:79756-69-7 TPI-1, also known as Tyrosine Phosphatase Inhibitor 1, is a SHP-1 inhibitor; inhibits recombinant SHP-1 with an IC50 of 40 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.
![Medchemexpress LLC 3-[(4-chlorophenyl)methoxy]-N-[(1S)-1-phenylethyl]thiophene-2-carboxamide | 1203680-76-5 | MFCD18086887 | >98.0% | 371.88 g/mol | C20H18ClNO2S | 10 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000298301.png-250.jpg)
Medchemexpress LLC 3-[(4-chlorophenyl)methoxy]-N-[(1S)-1-phenylethyl]thiophene-2-carboxamide | 1203680-76-5 | MFCD18086887 | >98.0% | 371.88 g/mol | C20H18ClNO2S | 10 MG
AS1949490 (3-[(4-chlorophenyl)methoxy]-N-[(1S)-1-phenylethyl]thiophene-2-carboxamide) is a potent, orally active, and selective inhibitor of SHIP2 phosphatase used for research into insulin signaling and metabolic disease. It increases Akt phosphorylation, glucose consumption, and glucose uptake in cellular models. Intended for research use only, it has a molecular weight of 371.88 g/mol and CAS 1203680-76-5.
- Selective SHIP2 inhibitor with nanomolar activity for mouse and human SHIP2.
- Promotes Akt phosphorylation and increases glucose uptake in cells.
- Suitable for metabolic and diabetes research applications.
- Molecular formula C20H18ClNO2S and molecular weight 371.88 g/mol.
- Typical supplier-reported purity ≥98% (HPLC).
- Powder stable at -20 °C; in solution stable at -80 °C (6 months) or -20 °C (1 month).
Medchemexpress LLC Suprofen | 40828-46-4 | 99.1% | 50 MG
Suprofen (TN-762) is a non-steroidal anti-inflammatory drug (NSAID) and an ibuprofen-type anti-inflammatory analgesic and antipyretic. It inhibits prostaglandin synthesis and has been proposed as an anti-arthritic. It is intended for research use only.
- Non-steroidal anti-inflammatory drug (NSAID)
- Inhibits prostaglandin synthesis
- Purity of 99.1%
- Molecular weight: 260.31
- Chemical formula: C14H12O3S
- Solid, white to off-white appearance
- Recommended storage as powder: -20°C for 3 years, 4°C for 2 years
- Recommended storage in solvent: -80°C for 2 years, -20°C for 1 year
- Soluble in DMSO at ≥ 100 mg/mL
- For research use only
Medchemexpress LLC IL-17 modulator 4 | 2446803-65-0 | 99.0% | C27H34N6O2 | 100 MG
IL-17 modulator 4 | 2446803-65-0 | 99.0% | C27H34N6O2 | 100 MG
Medchemexpress LLC HY-13439 5mg Medchemexpress, SR144528 CAS:192703-06-3 Purity:>98%
Medchemexpress, HY-13439 5mg SR144528 CAS:192703-06-3 SR144528 is a potent and selective CB2 receptor antagonist with a Ki of 0.6 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.
eMolecules Medchem Express / Gamma-Mangostin / 5mg / 518571349 / HY-N1957 / / 31271-07-5 / MFCD00951752 / 396.439 / C23H24O6
Medchem Express / Gamma-Mangostin / 5mg / 518571349 / HY-N1957 / / 31271-07-5 / MFCD00951752 / 396.439 / C23H24O6
Apexbio Technology LLC Tylosin phosphate 1405-53-4 50mg
Tylosin phosphate (CAS 1405-53-4) is a small-molecule inhibitor targeting bacterial ribosomal subunits It is designed to interfere with bacterial translation thereby inhibiting bacterial protein synthesis Tylosin phosphate exerts its biological activity primarily through binding to ribosomal subunits of Gram-positive bacteria In in vitro studies tylosin phosphate demonstrates inhibitory activity with reported IC50 values generally ranging between 0 5 5 g/mL depending on bacterial strain and assay conditions Based on these pharmacological properties tylosin phosphate holds research potential in studies of antibiotic resistance mechanisms antibacterial spectrum evaluation and as an antibiotic additive to explore growth promotion and therapeutic utility in poultry swine and bovine models
eMolecules Medchem Express / Pyr3 / 5mg / 446259346 / HY-108465 / / 1160514-60-2 / MFCD00178741 / 456.630 / C16H11Cl3F3N3O3
Medchem Express / Pyr3 / 5mg / 446259346 / HY-108465 / / 1160514-60-2 / MFCD00178741 / 456.630 / C16H11Cl3F3N3O3
eMolecules Medchem Express / ML218 / 5mg / 437898989 / HY-103309 / / 1346233-68-8 / MFCD23704169 / 369.330 / C19H26Cl2N2O
Medchem Express / ML218 / 5mg / 437898989 / HY-103309 / / 1346233-68-8 / MFCD23704169 / 369.330 / C19H26Cl2N2O