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Filtered Search Results
eMolecules EMOLECULES INC
NC3962245 1-2-PYRIDINYL-4-PIPERIDINAMINE
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![eMolecules 8-azabicyclo[3.2.1]octan-2-one hydrochloride | 2007921-32-4 | MFCD30471643 | 1g](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502147489.JPG-250.jpg)
eMolecules 8-azabicyclo[3.2.1]octan-2-one hydrochloride | 2007921-32-4 | MFCD30471643 | 1g
J&W PharmLab LLC | 8-azabicyclo[3.2.1]octan-2-one hydrochloride | 1g | 599148070 | 60R1131S | 98.000 | 2007921-32-4 | MFCD30471643 | 161.630 | C7H12ClNO
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![eMolecules Medchem Express / Boc-bipiperidine-ethynylbenzoic acid / 5mg / 742367649 / HY-139661 / / 2308497-81-4 / [null] / 412.530 / C24H32N2O4](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502458721.PNG-250.jpg)
eMolecules Medchem Express / Boc-bipiperidine-ethynylbenzoic acid / 5mg / 742367649 / HY-139661 / / 2308497-81-4 / [null] / 412.530 / C24H32N2O4
Medchem Express / Boc-bipiperidine-ethynylbenzoic acid / 5mg / 742367649 / HY-139661 / / 2308497-81-4 / [null] / 412.530 / C24H32N2O4
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Chem-Impex International, Inc. 1-Boc-4-aminopiperidine | MFCD01076201 | 100G
1-Boc-4-aminopiperidine, MFCD01076201, 100G
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Medchemexpress LLC N1-(4-methylphenyl)-N2-(2,2,6,6-tetramethyl-4-piperidinyl)ethanediamide | 144217-65-2 | 99.0% | 317.43 | C18H27N3O2 | 100 MG
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YYA-021 is a small-molecule CD4 mimic that inhibits HIV entry, exhibiting high anti-HIV activity and low cytotoxicity. It is provided for research use to study HIV entry mechanisms, antiviral screening, and cell-based assay development.
- Small-molecule CD4 mimic that targets gp120-mediated entry.
- Inhibits HIV entry with demonstrated antiviral activity.
- Low cytotoxicity suitable for cell-based assays.
- Well-characterized chemical properties: C18H27N3O2; molecular weight 317.43.
- High purity for research applications (>98.9%).
- Stable solid; recommended storage at -20°C (powder) and -80°C (in solvent).
- Supplied in milligram quantities convenient for assay development.
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Chembridge Corporation TERT-BUTYL 4-AMINOPIPERIDINE-1
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tert-butyl 4-amino-1-piperidinecarboxylate hydrochloride; CAS: 189819-75-8
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Medchemexpress LLC HY-50940 10mg Medchemexpress, AT7519 CAS:844442-38-2 Purity:>98%
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Medchemexpress, HY-50940 10mg AT7519 CAS:844442-38-2 AT7519 as a potent inhibitor of CDKs, with IC50s of 210, 47, 100, 13, 170, and <10 nM for CDK1, CDK2, CDK4 to CDK6, and CDK9, 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 HY-100388 100mg Medchemexpress, SHP099 CAS:1801747-42-1 Purity:98%
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Medchemexpress,HY-100388 100mg SHP099 CAS:1801747-42-1 Formula:C16H19Cl2N5 SHP099 is a potent, selective, orally available SHP2 inhibitor with an IC50 of 70 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 HY-13223 100mg , Crenolanib CP-868596 CAS:670220-88-9 Purity:98%
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Medchemexpress, HY-13223 100mg Crenolanib CP-868596 CAS:670220-88-9 Formula:C26H29N5O2 Kd: 2.1 nM (PDGFRα), 3.2 nM (PDGFRβ), 0.74 nM (FLT3) Purity:98% Crenolanib is a potent and selective inhibitor of PDGFRα/β , FLT3 with K d of 2.1 nM/3.2 nM, 0.74 nM, respectively, sensitive to D842V mutation not V561D mutation, and > 100-fold more selective for PDGFR than c-Kit, VEGFR-2, TIE-2, FGFR-2, EGFR, erbB2, and Src. 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 Alectinib S2762-50mg
Alectinib is a potent ALK inhibitor with IC50 of 1 9 nM in cell-free assays sensitive to L1196M mutation and higher selectivity for ALK than PF-02341066 NVP-TAE684 and PHA-E429
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![eMolecules [(3S)-1-methylpiperidin-3-yl]methanamine dihydrochloride | 1400744-19-5 | MFCD21641985 | 1g](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502136917.JPG-250.jpg)
eMolecules [(3S)-1-methylpiperidin-3-yl]methanamine dihydrochloride | 1400744-19-5 | MFCD21641985 | 1g
Pharmablock | [(3S)-1-methylpiperidin-3-yl]methanamine dihydrochloride | 1g | 551059902 | PB00921-01 | | 1400744-19-5 | MFCD21641985 | 201.140 | C7H18Cl2N2
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![eMolecules N-CBZ-8-AZABICYCLO[3.2.1]OCTANE-3-CARBOXYLIC ACID | 1159822-23-7 | MFCD27940040 | 1g](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502172150.JPG-250.jpg)
eMolecules N-CBZ-8-AZABICYCLO[3.2.1]OCTANE-3-CARBOXYLIC ACID | 1159822-23-7 | MFCD27940040 | 1g
AstaTech | N-CBZ-8-AZABICYCLO[3.2.1]OCTANE-3-CARBOXYLIC ACID | 1g | 112524949 | 57099 | 97.000 | 1159822-23-7 | MFCD27940040 | 289.331 | C16H19NO4
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eMolecules 4-AMINOPIPERIDIN-2-ONE HCL | 1260883-24-6 | MFCD12913634 | 1g
AstaTech | 4-AMINOPIPERIDIN-2-ONE HCL | 1g | 233622788 | 27397 | 95.000 | 1260883-24-6 | MFCD12913634 | 150.610 | C5H11ClN2O
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Medchemexpress LLC DDO-2213 | 2378768-36-4 | C24H27ClFN7O | 5 MG
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DDO-2213 is an orally active and potent WDR5-MLL1 inhibitor, with an IC50 of 29 nM and a Kd value of 72.9 nM for the WDR5 protein. It selectively inhibits MLL (mixed lineage leukemia) histone methyltransferase activity and the proliferation of MLL translocation-harboring cells. DDO-2213 can be used for MLL fusion leukemia research.
- Orally active
- Potent WDR5-MLL1 inhibitor
- Selectively inhibits MLL histone methyltransferase activity
- Inhibits proliferation of MLL translocation-harboring cells
- Useful for MLL fusion leukemia research
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Medchemexpress LLC DDO-2213 | 2378768-36-4 | C24H27ClFN7O | 100 MG
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DDO-2213 is an orally active and potent WDR5-MLL1 inhibitor. It selectively inhibits MLL histone methyltransferase activity and the proliferation of MLL translocation-harboring cells.
- Orally active and potent WDR5-MLL1 inhibitor
- Selectively inhibits MLL histone methyltransferase activity
- Inhibits proliferation of MLL translocation-harboring cells
- Suitable for MLL fusion leukemia research
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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