Drug Information
Drug General Information | |||||
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Drug ID |
D0F4JL
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Former ID |
DNC007822
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Drug Name |
NSC-661755
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Indication | Discovery agent | Terminated | [1] | ||
Structure |
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Download2D MOL |
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Canonical SMILES |
CC1CC2=C(C(=CC(=C2C(N1)C)O)O)C3=CC(=C(C4=C(C=C(C=C34)C)<br />OC)O)C5=C(C6=C(C=C(C=C6C(=C5)C7=C8CC(NC(C8=C(C=C7O)O)C)<br />C)C)OC)O.CC(=O)O
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InChI |
1S/C46H48N2O8.C2H4O2/c1-19-9-25-27(41-31-13-21(3)47-23(5)39(31)33(49)17-35(41)51)15-29(45(53)43(25)37(11-19)55-7)30-16-28(26-10-20(2)12-38(56-8)44(26)46(30)54)42-32-14-22(4)48-24(6)40(32)34(50)18-36(42)52;1-2(3)4/h9-12,15-18,21-24,47-54H,13-14H2,1-8H3;1H3,(H,3,4)/t21-,22-,23-,24-;/m0./s1
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InChIKey |
IHCBLDDSPLYUGN-JPIABUGISA-N
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Target and Pathway | |||||
Target(s) | Arachidonate 12-lipoxygenase, 12S-type | Target Info | Inhibitor | [2] | |
Arachidonate 15-lipoxygenase | Target Info | Inhibitor | [2] | ||
BioCyc Pathway | Lipoxin biosynthesisPWY66-397:Resolvin D biosynthesis | ||||
Lipoxin biosynthesis | |||||
KEGG Pathway | Arachidonic acid metabolism | ||||
Metabolic pathways | |||||
Serotonergic synapse | |||||
Inflammatory mediator regulation of TRP channelshsa00590:Arachidonic acid metabolism | |||||
Linoleic acid metabolism | |||||
NetPath Pathway | IL4 Signaling Pathway | ||||
PANTHER Pathway | Inflammation mediated by chemokine and cytokine signaling pathwayP00031:Inflammation mediated by chemokine and cytokine signaling pathway | ||||
Pathway Interaction Database | IL4-mediated signaling events | ||||
PathWhiz Pathway | Arachidonic Acid MetabolismPW000044:Arachidonic Acid Metabolism | ||||
WikiPathways | Arachidonic acid metabolism | ||||
Eicosanoid SynthesisWP2650:Arachidonic acid metabolism | |||||
Eicosanoid Synthesis | |||||
References | |||||
REF 1 | Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800004041) | ||||
REF 2 | Bioorg Med Chem. 2007 Nov 15;15(22):6900-8. Epub 2007 Aug 22.Discovery of platelet-type 12-human lipoxygenase selective inhibitors by high-throughput screening of structurally diverse libraries. | ||||
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