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Filtered Search Results
eMolecules 596812-34-9 | 4-tert-Butyl-4'-fluorobenzhydrol | Oakwood Chemical | MFCD06201331 | 258.336 | C17H19FO | 97.000 | CC(C)(C)c1ccc(cc1)C(O)c1ccc(F)cc1 | 1g | 537680196
4-tert-Butyl-4'-fluorobenzhydrol | Oakwood Chemical | 596812-34-9 | MFCD06201331 | 258.336 | C17H19FO | 97.000 | CC(C)(C)c1ccc(cc1)C(O)c1ccc(F)cc1 | 1g | 537680196
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eMolecules 1204707-73-2 | Medchem Express | SRT3190 | 10mg | 446262255 | HY-13021 | MFCD19443645 | 475.53 | C18H23F2N5O4S2
AstaTech | 9-BROMO-23-DIIODO-56-DIHYDROBENZO[F]IMIDAZO[12-D][14]OXAZEPINE | 1g | 696740899 | E70262 | 95.000 | 1282516-68-0 | MFCD28358731 | 516.903 | C11H7BrI2N2O
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Medchemexpress LLC PRX-07034 hydrochloride | 903580-39-2 | 99.0% | C21H29Cl2N3O4S | 10MG
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PRX-07034 hydrochloride is a research-grade, selective 5-HT6 receptor antagonist supplied as a white to off-white solid. It is intended for laboratory research to support studies of cognition and memory and is not for human use.
- Potent 5-HT6 receptor antagonist (Ki = 4-8 nM; IC50 = 19 nM).
- High purity (98.97%) suitable for research applications.
- White to off-white solid, easy to weigh and handle.
- Stable when stored sealed and away from moisture; recommended storage at -20°C.
- Intended for preclinical and in vitro research use only.
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Medchemexpress LLC HY-107455 1mg Medchemexpress, A-485 CAS:1889279-16-6 Purity:>98%
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Medchemexpress, HY-107455 1mg A-485 CAS:1889279-16-6 A-485 is a potent and selective catalytic inhibitor of p300/CBP with IC50s of 9.8 nM and 2.6 nM for p300 and CBP histone acetyltransferase (HAT), 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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Medchemexpress LLC Abemaciclib metabolite M20 (LSN3106726) | 2138499-06-4 | 95.9% | 50 MG
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Abemaciclib metabolite M20 is the active metabolite of Abemaciclib and acts as a selective CDK4/6 inhibitor for the treatment of cancer. It is for research use only.
- Active metabolite of abemaciclib
- Selective CDK4/6 inhibitor
- Induces senescence in breast cancer cells
- Inhibits growth and cell cycle progression of NSCLC, colorectal, and breast cancer cells
- IC50 value for CDK4 and CDK6 in the range of 1-3 nM
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STA Pharmaceutical Fmoc-L-2-Chloro-4-fluorophe | 5 g | CAS 1217789-59-7 | MDL MFCD12198164
Fmoc-L-2-Chloro-4-fluorophe is a Amino Acid reagent (Subcategory: Phe) sold by WuXi TIDES. Offered in 5 g. Store at 4 °C. SDS available for reference.
Specifications
- CAS: 1217789-59-7
- MDL: MFCD12198164
- InChIKey: SPOFFSUHDCOUGW-QFIPXVFZSA-N
- Molecular Weight: 439.867
- Molecular Formula: C24H19ClFNO4
- Purity: ≥95%
- Container Type: 30 mL HDPE
- Pack Size: 5 g
- Net Weight: 5 g
- Gross Weight: 16.5 g
- Commodity Code: 29242970
- Country Of Origin: China
- IUPAC: (S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(2-chloro-4-fluorophenyl)propanoic acid
- SMILES: FC1=CC(Cl)=C(C[C@H](NC(OCC2C3=CC=CC=C3C4=CC=CC=C42)=O)C(O)=O)C=C1
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eMolecules 885060-08-2 | Medchem Express | (R)-Filanesib | 5mg | 446265114 | HY-15187A | MFCD23097098 | 420.48 | C20H22F2N4O2S
Medchem Express | (R)-Filanesib | 5mg | 446265114 | HY-15187A | 885060-08-2 | MFCD23097098 | 420.480 | C20H22F2N4O2S
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Medchemexpress LLC Abemaciclib metabolite M20 | 2138499-06-4 | 98.2% | 100 MG
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Abemaciclib metabolite M20 (LSN3106726) is the active metabolite of Abemaciclib and a selective CDK4/6 inhibitor for the treatment of cancer. It induces senescence in breast cancer cells at concentrations of 200 nM and 500 nM over 6-8 days.
- Induces senescence in breast cancer cells.
- Inhibits the growth and cell cycle progression of non-small cell lung cancer (NSCLC) cells, colorectal cancer (CRC) cells, and breast cancer cells.
- IC50 value for CDK4 and CDK6 is in the range of 1-3 nM.
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Aobchem 2-Chloro-6-fluorophenylboronic acid, AOBCHEM USA 11446-25G. 313545-32-3. MFCD04039892
2-Chloro-6-fluorophenylboronic acid, AOBCHEM USA 11446-25G. 313545-32-3. MFCD04039892
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eMolecules 879487-87-3 | R268712 | MFCD28963939 | 50mg
Ambeed | R268712 | 50mg | 572143336 | A158772 | 879487-87-3 | MFCD28963939 | 363.396 | C20H18FN5O
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STA Pharmaceutical Fmoc-(R)-3-Amino-4-(pentafluoro-phenyl)-butyric acid | 10 g | CAS 269398-94-9 | MDL MFCD01860941
Fmoc-(R)-3-Amino-4-(pentafluoro-phenyl)-butyric acid is a Amino Acid reagent (Subcategory: Beta AA) sold by WuXi TIDES. Offered in 10 g. Store at 4 °C. SDS available for reference.
Specifications
- CAS: 269398-94-9
- MDL: MFCD01860941
- InChIKey: HCBMYXPXBOUBBR-GFCCVEGCSA-N
- Molecular Weight: 491.414
- Molecular Formula: C25H18F5NO4
- Purity: ≥95%
- Container Type: 60 mL HDPE
- Pack Size: 10 g
- Net Weight: 10 g
- Gross Weight: 25 g
- Commodity Code: 29242970
- Country Of Origin: China
- IUPAC: (R)-3-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-(perfluorophenyl)butanoic acid
- SMILES: FC1=C(C(F)=C(C(F)=C1C[C@@H](NC(OCC2C3=CC=CC=C3C4=CC=CC=C42)=O)CC(O)=O)F)F
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eMolecules 3069-42-9 | Trimethoxy(octadecyl)silane | MFCD00043060 | 25g
Medchem Express | GS-6201 | 5mg | 506403356 | HY-10081 | 752222-83-6 | 446.434 | C21H21F3N6O2
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eMolecules 7116-38-3 | Ethyl 3-(4-fluorophenyl)propanoate | Combi-Blocks | MFCD07772966 | 196.221 | C11H13FO2 | 98.000 | CCOC(=O)CCc1ccc(F)cc1 | 25g | 517060717
Ethyl 3-(4-fluorophenyl)propanoate | Combi-Blocks | 7116-38-3 | MFCD07772966 | 196.221 | C11H13FO2 | 98.000 | CCOC(=O)CCc1ccc(F)cc1 | 25g | 517060717
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Matrix Scientific 2,3-DIFLUOROPHENYLBORONIC A-5G
2,3-Difluorophenylboronic acid, 98%; 5g,C6H5BF2O2, MFCD01863170, mw 157.91, [121219-16-7]
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![Medchemexpress LLC N-[3-[(3,4-dihydro-2,4-dioxo-3-propylthieno[3,2-d]pyrimidin-1(2H)-yl)methyl]phenyl]-benzeneacetamide | 2098776-03-3 | 98.4% | C24H23N3O3S | 10MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000260013.png-250.jpg)
Medchemexpress LLC N-[3-[(3,4-dihydro-2,4-dioxo-3-propylthieno[3,2-d]pyrimidin-1(2H)-yl)methyl]phenyl]-benzeneacetamide | 2098776-03-3 | 98.4% | C24H23N3O3S | 10MG
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FEN1-IN-SC13 is a small-molecule inhibitor of flap endonuclease 1 (FEN1) used for preclinical research into DNA replication, repair, and antitumor effects. It inhibits FEN1 activity in vitro and in cells, impairing DNA processing and increasing sensitivity to DNA-damaging agents. Supplied as a powder with high reported purity for laboratory research use only.
- Potent FEN1 inhibition in vitro and in cells.
- Interferes with DNA replication and repair pathways.
- Demonstrated antitumor activity in xenograft models.
- High purity suitable for biochemical and cellular assays.
- Powder form with recommended low-temperature storage.
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