FMX
FAMOXADONE
Created: | 2002-02-25 |
Last modified: | 2020-06-05 |
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Chemical Details | |
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Formal Charge | 0 |
Atom Count | 46 |
Chiral Atom Count | 1 |
Bond Count | 49 |
Aromatic Bond Count | 18 |
Chemical Component Summary | |
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Name | FAMOXADONE |
Synonyms | 5-METHYL-5-(4-PHENOXYPHENYL)-3-(PHENYLAMINO)-2,4-OXAZOLIDINEDIONE |
Systematic Name (OpenEye OEToolkits) | (5S)-5-methyl-5-(4-phenoxyphenyl)-3-phenylazanyl-1,3-oxazolidine-2,4-dione |
Formula | C22 H18 N2 O4 |
Molecular Weight | 374.389 |
Type | NON-POLYMER |
Chemical Descriptors | |||
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Type | Program | Version | Descriptor |
SMILES | ACDLabs | 10.04 | O=C2OC(C(=O)N2Nc1ccccc1)(c4ccc(Oc3ccccc3)cc4)C |
SMILES | CACTVS | 3.341 | C[C]1(OC(=O)N(Nc2ccccc2)C1=O)c3ccc(Oc4ccccc4)cc3 |
SMILES | OpenEye OEToolkits | 1.5.0 | CC1(C(=O)N(C(=O)O1)Nc2ccccc2)c3ccc(cc3)Oc4ccccc4 |
Canonical SMILES | CACTVS | 3.341 | C[C@]1(OC(=O)N(Nc2ccccc2)C1=O)c3ccc(Oc4ccccc4)cc3 |
Canonical SMILES | OpenEye OEToolkits | 1.5.0 | C[C@@]1(C(=O)N(C(=O)O1)Nc2ccccc2)c3ccc(cc3)Oc4ccccc4 |
InChI | InChI | 1.03 | InChI=1S/C22H18N2O4/c1-22(16-12-14-19(15-13-16)27-18-10-6-3-7-11-18)20(25)24(21(26)28-22)23-17-8-4-2-5-9-17/h2-15,23H,1H3/t22-/m0/s1 |
InChIKey | InChI | 1.03 | PCCSBWNGDMYFCW-QFIPXVFZSA-N |
Drug Info: DrugBank
DrugBank ID | DB07778 |
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Name | (S)-famoxadone |
Groups | experimental |
Synonyms |
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CAS number | 132584-12-4 |
Drug Targets
Name | Target Sequence | Pharmacological Action | Actions |
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Cytochrome c1, heme protein, mitochondrial | MAAAAASLRGVVLGPRGAGLPGARARGLLCSARPGQLPLRTPQAVALSSK... | unknown | |
Cytochrome b | MTPMRKTNPLMKLINHSFIDLPTPSNISAWWNFGSLLGACLILQITTGLF... | unknown | |
Cytochrome b-c1 complex subunit 1, mitochondrial | MAASVVCRAATAGAQVLLRARRSPALLRTPALRSTATFAQALQFVPETQV... | unknown | |
Cytochrome b-c1 complex subunit 2, mitochondrial | MKLLTRAGSFSRFYSLKVAPKVKATAAPAGAPPQPQDLEFTKLPNGLVIA... | unknown | |
Cytochrome b-c1 complex subunit 6, mitochondrial | MGLEDEQKMLTESGDPEEEEEEEEELVDPLTTVREQCEQLEKCVKARERL... | unknown | |
View More |
Drug Info/Drug Targets: DrugBank 3.0: a comprehensive resource for 'omics' research on drugs. Knox C, Law V, Jewison
T, Liu P, Ly S, Frolkis A, Pon A, Banco K, Mak C, Neveu V, Djoumbou Y, Eisner R, Guo AC, Wishart DS.
Nucleic Acids Res. 2011 Jan; 39 (Database issue):D1035-41. | PMID:21059682
Related Resource References
Resource Name | Reference |
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PubChem | 446845 |
ChEMBL | CHEMBL10118 |
ChEBI | CHEBI:106738 |
CCDC/CSD | XALTIN, XALTIN01 |