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Search for Small Molecules by SMILES, name, CAS, MFCD, ID, InChI Key
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IUPAC Name: 
N-[(1-cyclobutyl-1H-pyrazol-4-yl)methyl]-2,3,5,6-tetrafluoro-4-methoxyaniline
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Enamine Ltd
Ships from: Ukraine
To:
TBD 104
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Zoom the structure CSSS15281904801 Add to cart
IUPAC Name: 
1,2,4,5-tetrafluoro-3-nitro-6-[(4-phenylbut-3-yn-1-yl)oxy]benzene
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ChemBridge Corp.
Ships from: United States
To:
14 days 68
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Description: Name: 1,2,4,5-tetrafluoro-3-nitro-6-[(4-phenyl-3-butyn-1-yl)oxy]benzene; Stereochemistry: achiral; Compound state: solid
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Zoom the structure CSSS00132632482 Add to cart
IUPAC Name: 
5-{4-[2,6-difluoro-4-(2-methoxyethoxy)phenyl]piperazin-1-yl}-3-methyl-3H,4H,7H-[1,2,3]triazolo[4,5-d]pyrimidin-7-one
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MedChemExpress
Ships from: United States
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10 days 345
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Description: Names: Basroparib; STP1002; Product Description: Basroparib is an orally active poly (ADP-ribose) polymerase (PARP) inhibitor with an IC 50 of 5.8 nM for TNKS1 , exhibiting antitumor activity .; Target: PARP; CAS: 1858179-75-5
MedChemExpress EU
Ships from: Sweden
To:
10 days 363
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Description: Names: Basroparib; STP1002; Product Description: Basroparib is an orally active poly (ADP-ribose) polymerase (PARP) inhibitor with an IC50 of 5.8 nM for TNKS1, exhibiting antitumor activity; Target: PARP; CAS: 1858179-75-5
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Zoom the structure CSSS06657275931 Add to cart
IUPAC Name: 
1-phenyl-N-(2,3,6-trifluoro-4-{[3-(2-{[(3S,5S)-5-fluoropiperidin-3-yl]amino}pyrimidin-4-yl)pyridin-2-yl]oxy}phenyl)methanesulfonamide
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MedChemExpress
Ships from: United States
To:
10 days 460
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Description: Names: G-5758; Product Description: G-5758 is an orally available IRE1α inhibitor with an IC 50 of 38 nM for XBP1s. G-5758 is well tolerated in multiple myeloma models (KMS-11) at oral doses up to 500 mg/kg in rats. G-5758 exhibits pharmacodynamics comparable to that of induced IRE1 knockdown .; Target: IRE1;Liposome; CAS: 2413455-99-7
MedChemExpress EU
Ships from: Sweden
To:
10 days 484
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Description: Names: G-5758; Product Description: G-5758 is an orally available IRE1α inhibitor with an IC50 of 38 nM for XBP1s. G-5758 is well tolerated in multiple myeloma models (KMS-11) at oral doses up to 500 mg/kg in rats. G-5758 exhibits pharmacodynamics comparable to that of induced IRE1 knockdown; Target: IRE1;Liposome; CAS: 2413455-99-7
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Zoom the structure CSSS20456218544 Add to cart
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