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Filtered Search Results
eMolecules 169751-73-9 | Ambeed | tert-Butyl 14-(tosyloxy)-36912-tetraoxatetradecan-1-oate | 100mg | 633662538 | A388377 | MFCD27977499 | 462.55 | C21H34O9S
Medchem Express | Glycolithocholic acid (sodium) | 5mg | 758391287 | HY-116374A | 24404-83-9 | MFCD00036744 | 455.615 | C26H42NNaO4
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Medchemexpress LLC ASN007 benzenesulfonate | 2055597-39-0 | 99.7% | 632.11 | C28H31ClFN7O5S | 5 MG
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ASN007 benzenesulfonate is the benzenesulfonate salt of ASN007, a potent ERK1/2 inhibitor used for preclinical research into MAPK/ERK pathway biology and cancers driven by RAS mutations. It is supplied as a high-purity research reagent for in vitro and in vivo studies.
- Potent ERK1/2 inhibition with low single-digit nanomolar IC50 values.
- Suitable for research of RAS- and MAPK/ERK-driven cancer models.
- Benzenesulfonate salt form for improved handling and stability.
- High purity (≈99.7%) suitable for biological studies.
- Molecular weight 632.11 and formula C28H31ClFN7O5S.
- Available in small reagent pack sizes for dose-response and pilot studies.
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Medchemexpress LLC Pulrodemstat benzenesulfonate | 2097523-60-7 | 99.6% | 10 MG
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Pulrodemstat benzenesulfonate (CC-90011) is a potent, selective, reversible, and orally active inhibitor of lysine specific demethylase-1 (LSD1) with an IC50 of 0.25 nM. It exhibits less enzymatic inhibition against LSD2, MAO-A, and MAO-B. This compound induces differentiation in acute myeloid leukemia (AML) and small cell lung cancer (SCLC) cells and demonstrates potent anticancer activity.
- Potent, selective, reversible, and orally active LSD1 inhibitor
- IC50 of 0.25 nM for LSD1
- Induces acute myeloid leukemia (AML) and small cell lung cancer (SCLC) cell differentiation
- Potent anticancer activity
- Less enzymatic inhibition against LSD2, MAO-A, and MAO-B
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![eMolecules 115314-17-5 | (R)-(-)-Glycidyl nosylate | Combi-Blocks | MFCD00013436 | 259.230 | C9H9NO6S | 97.000 | [O-][N+](=O)c1cccc(c1)S(=O)(=O)OC[C@H]1CO1 | 1g | 205387783](https://assets.fishersci.com/TFS-Assets/CCG/product-images/VN00128114-384134766.PNG-250.jpg)
eMolecules 115314-17-5 | (R)-(-)-Glycidyl nosylate | Combi-Blocks | MFCD00013436 | 259.230 | C9H9NO6S | 97.000 | [O-][N+](=O)c1cccc(c1)S(=O)(=O)OC[C@H]1CO1 | 1g | 205387783
(R)-(-)-Glycidyl nosylate | Combi-Blocks | 115314-17-5 | MFCD00013436 | 259.230 | C9H9NO6S | 97.000 | [O-][N+](=O)c1cccc(c1)S(=O)(=O)OC[C@H]1CO1 | 1g | 205387783
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eMolecules 512-35-6 | Benzenesulfonic anhydride | Combi-Blocks | MFCD00054601 | 298.330 | C12H10O5S2 | 96.000 | O=S(=O)(OS(=O)(=O)c1ccccc1)c1ccccc1 | 1g | 267199818
Benzenesulfonic anhydride | Combi-Blocks | 512-35-6 | MFCD00054601 | 298.330 | C12H10O5S2 | 96.000 | O=S(=O)(OS(=O)(=O)c1ccccc1)c1ccccc1 | 1g | 267199818
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Chemscene ChemScene | Ethoxydiphenylphosphine | 500G | CS-W010380 | 0.97 | 719-80-2| MFCD00009087 | 230.25
ChemScene | Ethoxydiphenylphosphine | 500G | CS-W010380 | 0.97 | 719-80-2| MFCD00009087 | 230.25
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Medchemexpress LLC Pulrodemstat benzenesulfonate | 2097523-60-7 | 99.6% | 50 MG
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Pulrodemstat benzenesulfonate is a potent, selective, reversible, and orally active inhibitor of lysine specific demethylase-1 (LSD1) with an IC50 of 0.25 nM. It induces differentiation in acute myeloid leukemia (AML) and small cell lung cancer (SCLC) cells, demonstrating potent anticancer activity.
- Potent, selective, reversible, and orally active LSD1 inhibitor
- Less enzymatic inhibition against LSD2, MAO-A, and MAO-B
- Induces differentiation in AML and SCLC cells
- Demonstrates potent anticancer activity
- Shows potent induction of CD11b in THP-1 cell line
- Exhibits antiproliferative activity in AML kasumi-1 cells
- Suppression of GRP observed in a dose-dependent manner
- Potent antiproliferative activity in SCLC cells
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Matrix Scientific 3-BUTYNYL P-TOLUENESULFONAT-5G
3-Butynyl p-toluenesulfonate, 98%; 5g,C11H12O3S, MFCD00041687, mw 224.28, [23418-85-1]
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Enovation Chemicals LLC METHANESULFONIC ACID,1-BROM 5G
Methanesulfonic acid,1-bromo-,sodium salt | Purity 97% | 34239-78-6 | MFCD00154894 | 5g
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eMolecules 164365-88-2 | 4-(Boc-amino)butyl Bromide | AA Blocks LLC | MFCD06201020 | 252.152 | C9H18BrNO2 | 0.000 | CC(C)(C)OC(=O)NCCCCBr | 100mg | 795062973
4-(Boc-amino)butyl Bromide | AA Blocks LLC | 164365-88-2 | MFCD06201020 | 252.152 | C9H18BrNO2 | 0.000 | CC(C)(C)OC(=O)NCCCCBr | 100mg | 795062973
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Medchemexpress LLC HY-108006 5mg Medchemexpress, Mirogabalin besylate CAS:1138245-21-2 Purity:>98%
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Medchemexpress, HY-108006 5mg Mirogabalin besylate CAS:1138245-21-2 Mirogabalin besylate is a selective and orally available ligand for the α2δ subunit of voltage-gated calcium channels, with Kds of 13.5 nM, 22.7 nM, 27 nM, and 47.6 nM for human α2δ-1, human α2δ-2, rat α2δ-1, and rat α2δ-2, respectively. 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 168021-79-2 | Medchem Express | Disufenton sodium | 10mg | 446262544 | HY-13244 | MFCD09833648 | 381.32 | C11H13NNa2O7S2
Medchem Express | HS271 | 5mg | 588504707 | HY-131903 | 2410393-15-4 | 435.451 | C21H24F3N5O2
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![eMolecules AstaTech / TERT-BUTYL 6-(TOSYLOXY)-2-AZASPIRO[3.3]HEPTANE-2-CARBOXYLATE / 0.1g / 793957256 / AT23473 / 95.000 / 1558037-97-0 / [null] / 367.460 / C18H25NO5S](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502461246.JPG-250.jpg)
eMolecules AstaTech / TERT-BUTYL 6-(TOSYLOXY)-2-AZASPIRO[3.3]HEPTANE-2-CARBOXYLATE / 0.1g / 793957256 / AT23473 / 95.000 / 1558037-97-0 / [null] / 367.460 / C18H25NO5S
AstaTech / TERT-BUTYL 6-(TOSYLOXY)-2-AZASPIRO[3.3]HEPTANE-2-CARBOXYLATE / 0.1g / 793957256 / AT23473 / 95.000 / 1558037-97-0 / [null] / 367.460 / C18H25NO5S
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Medchemexpress LLC ASN007 benzenesulfonate (ERK-IN-3 benzenesulfonate) | 2055597-39-0 | 99.7% | 632.11 | 100 MG
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ASN007 (ERK-IN-3) benzenesulfonate is a potent and orally active inhibitor of ERK. It demonstrates potent inhibition of ERK1/2 with low single-digit nanomolar IC50 values. This compound exhibits significant antiproliferative activity against various tumor cells and is suitable for research into cancers driven by RAS mutations.
- Potent and orally active ERK inhibitor
- Inhibits ERK1/2 with low single-digit nM IC50 values
- Exhibits significant antiproliferative activity against various tumor cells
- Useful for research of cancers driven by RAS mutations
- Inhibits the phosphorylation of ERK1/2 substrates (e.g., RSK1, FRA1, Elk1) in various cell lines
- Induces G0/G1 phase cell cycle arrest in various cells
- Significantly inhibits tumor growth and shows good tolerance in nude mice bearing BRAF and KRAS mutant xenograft tumors
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eMolecules 75-75-2 | METHANESULFONIC ACID | AstaTech96.100 | CH4O3S | 95.000 | CS(O)(=O)=O | 100g | 718056367
METHANESULFONIC ACID | AstaTech | 75-75-296.100 | CH4O3S | 95.000 | CS(O)(=O)=O | 100g | 718056367
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