(2S)-2-(5-{[(3-Methyl-1-oxo-1,2-dihydrobenzo[f]quinazolin-9-yl)me thyl]amino}-1-oxo-1,3-dihydro-2H-isoindol-2-yl)pentanedioic acid
Modify Date: 2025-10-09 17:42:10
![(2S)-2-(5-{[(3-Methyl-1-oxo-1,2-dihydrobenzo[f]quinazolin-9-yl)me thyl]amino}-1-oxo-1,3-dihydro-2H-isoindol-2-yl)pentanedioic acid Structure](https://image.chemsrc.com/caspic/139/139987-54-5.png)
(2S)-2-(5-{[(3-Methyl-1-oxo-1,2-dihydrobenzo[f]quinazolin-9-yl)me thyl]amino}-1-oxo-1,3-dihydro-2H-isoindol-2-yl)pentanedioic acid structure
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Common Name | (2S)-2-(5-{[(3-Methyl-1-oxo-1,2-dihydrobenzo[f]quinazolin-9-yl)me thyl]amino}-1-oxo-1,3-dihydro-2H-isoindol-2-yl)pentanedioic acid | ||
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| CAS Number | 139987-54-5 | Molecular Weight | 500.50300 | |
| Density | 1.5 g/cm3 | Boiling Point | 852.4ºC at 760 mmHg | |
| Molecular Formula | C27H24N4O6 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | 469.3ºC | |
| Name | (2S)-2-(5-{[(3-Methyl-1-oxo-1,2-dihydrobenzo[f]quinazolin-9-yl)me thyl]amino}-1-oxo-1,3-dihydro-2H-isoindol-2-yl)pentanedioic acid |
|---|
| Density | 1.5 g/cm3 |
|---|---|
| Boiling Point | 852.4ºC at 760 mmHg |
| Molecular Formula | C27H24N4O6 |
| Molecular Weight | 500.50300 |
| Flash Point | 469.3ºC |
| Exact Mass | 500.17000 |
| PSA | 152.95000 |
| LogP | 3.69380 |
| Vapour Pressure | 6.35E-31mmHg at 25°C |
| Index of Refraction | 1.728 |
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Name: Inhibition of Escherichia coli DHFR by spectrophotometry
Source: ChEMBL
Target: Dihydrofolate reductase
External Id: CHEMBL1819663
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Name: ST_JUDE_LEISH: Cytotoxicity at 2uM final concentration against transgenic Leishmania ...
Source: ChEMBL
Target: Glucose transporter
External Id: CHEMBL3436044
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Name: Inhibition of human DHFR by spectrophotometry
Source: ChEMBL
Target: Dihydrofolate reductase
External Id: CHEMBL1819662
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Name: ST_JUDE_LEISH: Cytotoxicity at 2uM final concentration against transgenic Leishmania ...
Source: ChEMBL
Target: Solute carrier family 2, facilitated glucose transporter member 1
External Id: CHEMBL3436042
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Name: Inhibition of Toxoplasma gondii DHFR by spectrophotometry
Source: ChEMBL
Target: Bifunctional dihydrofolate reductase-thymidylate synthase
External Id: CHEMBL1819664
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Name: ST_JUDE_LEISH: Cytotoxicity at 2uM final concentration against transgenic Leishmania ...
Source: ChEMBL
Target: Hexose transporter 1
External Id: CHEMBL3436043
|
|
Name: Experimentally measured binding affinity data (Ki) for protein-ligand complexes deriv...
Source: Shanghai Institute of Organic Chemistry
Target: N/A
External Id: PDBbind-Ki for protein-ligand complexes
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|
Name: Ratio of Vm and Km values, a measure of Substrate selectivity for hog liver folyl-pol...
Source: ChEMBL
Target: N/A
External Id: CHEMBL847699
|
|
Name: Inhibition of MTX uptake in MOLT-4 human T-cell leukemia cells
Source: ChEMBL
Target: MOLT-4
External Id: CHEMBL715935
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Name: The compound was tested for inhibitory activity against thymidylate synthase (purifie...
Source: ChEMBL
Target: Thymidylate synthase
External Id: CHEMBL811584
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