Drug General Information |
Drug ID |
D0Y6OA
|
Former ID |
DNC003732
|
Drug Name |
COUMATE
|
Indication |
Breast cancer [ICD9: 174, 175; ICD10:C50]
|
Phase 2 |
[1]
|
Structure |
|
Download
2D MOL
3D MOL
|
Target and Pathway |
Target(s) |
Carbonic anhydrase IV |
Target Info |
Inhibitor |
[2]
|
Carbonic anhydrase |
Target Info |
Inhibitor |
[2]
|
Carbonic anhydrase I |
Target Info |
Inhibitor |
[2]
|
Carbonic anhydrase XIV |
Target Info |
Inhibitor |
[2]
|
Carbonic anhydrase IX |
Target Info |
Inhibitor |
[2]
|
Carbonic anhydrase VI |
Target Info |
Inhibitor |
[2]
|
Steryl-sulfatase |
Target Info |
Inhibitor |
[3]
|
Carbonic anhydrase XII |
Target Info |
Inhibitor |
[2]
|
Cytochrome P450 19 |
Target Info |
Inhibitor |
[3]
|
Carbonic anhydrase II |
Target Info |
Inhibitor |
[2]
|
BioCyc Pathway
|
Superpathway of steroid hormone biosynthesis
|
Estradiol biosynthesis II
|
Estradiol biosynthesis I
|
KEGG Pathway
|
Nitrogen metabolism
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Proximal tubule bicarbonate reclamationhsa00910:Nitrogen metabolismhsa00910:Nitrogen metabolismhsa00910:Nitrogen metabolismhsa00910:Nitrogen metabolismhsa00140:Steroid hormone biosynthesishsa00910:Nitrogen metabolismhsa00140:Steroid hormone biosynthesis
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Metabolic pathways
|
Ovarian steroidogenesishsa00910:Nitrogen metabolism
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Proximal tubule bicarbonate reclamation
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Collecting duct acid secretion
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Gastric acid secretion
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Pancreatic secretion
|
Bile secretion
|
NetPath Pathway
|
TGF_beta_Receptor Signaling PathwayNetPath_25:FSH Signaling PathwayNetPath_16:IL4 Signaling Pathway
|
EGFR1 Signaling Pathway
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PANTHER Pathway
|
Androgen/estrogene/progesterone biosynthesis
|
Pathway Interaction Database
|
C-MYB transcription factor networkhif1_tfpathway:HIF-1-alpha transcription factor network
|
PathWhiz Pathway
|
Gastric Acid ProductionPW000045:Androgen and Estrogen MetabolismPW000045:Androgen and Estrogen Metabolism
|
Reactome
|
Erythrocytes take up carbon dioxide and release oxygen
|
Erythrocytes take up oxygen and release carbon dioxide
|
Reversible hydration of carbon dioxideR-HSA-1237044:Erythrocytes take up carbon dioxide and release oxygen
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Reversible hydration of carbon dioxideR-HSA-1475029:Reversible hydration of carbon dioxideR-HSA-1234158:Regulation of gene expression by Hypoxia-inducible Factor
|
Reversible hydration of carbon dioxideR-HSA-1475029:Reversible hydration of carbon dioxideR-HSA-1660662:Glycosphingolipid metabolismR-HSA-1475029:Reversible hydration of carbon dioxideR-HSA-211976:Endogenous sterolsR-HSA-1237044:Erythrocytes take up carbon dioxide and release oxygen
|
Reversible hydration of carbon dioxide
|
WikiPathways
|
Reversible Hydration of Carbon Dioxide
|
Uptake of Carbon Dioxide and Release of Oxygen by Erythrocytes
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Uptake of Oxygen and Release of Carbon Dioxide by ErythrocytesWP2770:Reversible Hydration of Carbon Dioxide
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Uptake of Oxygen and Release of Carbon Dioxide by ErythrocytesWP2770:Reversible Hydration of Carbon DioxideWP2877:Vitamin D Receptor Pathway
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Regulation of Hypoxia-inducible Factor (HIF) by OxygenWP2770:Reversible Hydration of Carbon DioxideWP697:Estrogen metabolism
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Vitamin D Receptor Pathway
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Sphingolipid metabolismWP2770:Reversible Hydration of Carbon Dioxide
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miR-targeted genes in muscle cell - TarBase
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miR-targeted genes in leukocytes - TarBase
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miR-targeted genes in epithelium - TarBaseWP702:Metapathway biotransformation
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Tryptophan metabolism
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Oxidation by Cytochrome P450
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Ovarian Infertility Genes
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Metabolism of steroid hormones and vitamin D
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FSH signaling pathway
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Integrated Breast Cancer Pathway
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Phase 1 - Functionalization of compoundsWP2770:Reversible Hydration of Carbon Dioxide
|
Uptake of Oxygen and Release of Carbon Dioxide by Erythrocytes
|
References |
REF 1 | Irosustat: a first-generation steroid sulfatase inhibitor in breast cancer. Expert Rev Anticancer Ther. 2011 Feb;11(2):179-83. |
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REF 2 | Bioorg Med Chem Lett. 2008 Aug 1;18(15):4282-6. Epub 2008 Jul 5.Carbonic anhydrase inhibitors. Interaction of the antitumor sulfamate EMD 486019 with twelve mammalian carbonic anhydrase isoforms: Kinetic and X-ray crystallographic studies. |
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REF 3 | J Med Chem. 2010 Mar 11;53(5):2155-70.Highly potent first examples of dual aromatase-steroid sulfatase inhibitors based on a biphenyl template. |