General Information of Drug Off-Target (DOT) (ID: OTV729DT)

DOT Name Dehydrogenase/reductase SDR family member 7 (DHRS7)
Synonyms EC 1.1.1.-; Retinal short-chain dehydrogenase/reductase 4; retSDR4; Short chain dehydrogenase/reductase family 34C member 1; Protein SDR34C1
Gene Name DHRS7
UniProt ID
DHRS7_HUMAN
3D Structure
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2D Sequence (FASTA)
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3D Structure (PDB)
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EC Number
1.1.1.-
Pfam ID
PF00106
Sequence
MNWELLLWLLVLCALLLLLVQLLRFLRADGDLTLLWAEWQGRRPEWELTDMVVWVTGASS
GIGEELAYQLSKLGVSLVLSARRVHELERVKRRCLENGNLKEKDILVLPLDLTDTGSHEA
ATKAVLQEFGRIDILVNNGGMSQRSLCMDTSLDVYRKLIELNYLGTVSLTKCVLPHMIER
KQGKIVTVNSILGIISVPLSIGYCASKHALRGFFNGLRTELATYPGIIVSNICPGPVQSN
IVENSLAGEVTKTIGNNGDQSHKMTTSRCVRLMLISMANDLKEVWISEQPFLLVTYLWQY
MPTWAWWITNKMGKKRIENFKSGVDADSSYFKIFKTKHD
Function
NADPH-dependent oxidoreductase which catalyzes the reduction of a variety of compounds bearing carbonyl groups including steroids, retinoids and xenobiotics. Catalyzes the reduction/inactivation of 5alpha-dihydrotestosterone to 3alpha-androstanediol, with a possible role in the modulation of androgen receptor function. Involved in the reduction of all-trans-retinal to all-trans-retinol. Converts cortisone to 20beta-dihydrocortisone in vitro, although the physiological relevance of this activity is questionable. Reduces exogenous compounds such as quinones (1,2-naphtoquinone, 9,10-phenantrenequinone and benzoquinone) and other xenobiotics (alpha-diketones) in vitro, suggesting a role in the biotransformation of xenobiotics with carbonyl group. A dehydrogenase activity has not been detected so far. May play a role as tumor suppressor.
Tissue Specificity Found predominantly in the adrenal glands, liver, thyroid, prostate, small intestine, colon, stomach, kidney and brain . Lower levels observed in skeletal muscle, the lung and the spleen .

Molecular Interaction Atlas (MIA) of This DOT

Molecular Interaction Atlas (MIA) Jump to Detail Molecular Interaction Atlas of This DOT
This DOT Affected the Biotransformations of 12 Drug(s)
Drug Name Drug ID Highest Status Interaction REF
Estrone DM5T6US Approved Dehydrogenase/reductase SDR family member 7 (DHRS7) increases the reduction of Estrone. [17]
Oxcarbazepine DM5PU6O Approved Dehydrogenase/reductase SDR family member 7 (DHRS7) increases the reduction of Oxcarbazepine. [17]
Metyrapone DMI7FVQ Approved Dehydrogenase/reductase SDR family member 7 (DHRS7) increases the reduction of Metyrapone. [17]
Cortisone DMU5QZX Approved Dehydrogenase/reductase SDR family member 7 (DHRS7) increases the reduction of Cortisone. [17]
BRN-3548355 DM4KXT0 Investigative Dehydrogenase/reductase SDR family member 7 (DHRS7) increases the reduction of BRN-3548355. [17]
Benzoquinone DMNBA0G Investigative Dehydrogenase/reductase SDR family member 7 (DHRS7) increases the reduction of Benzoquinone. [17]
Phenanthrene-9,10-dione DMG8KS9 Investigative Dehydrogenase/reductase SDR family member 7 (DHRS7) increases the reduction of Phenanthrene-9,10-dione. [17]
4-ANDROSTENE-3-17-DIONE DMSE8NU Investigative Dehydrogenase/reductase SDR family member 7 (DHRS7) increases the reduction of 4-ANDROSTENE-3-17-DIONE. [17]
1,2-NAPHTHOQUINONE DMYXELH Investigative Dehydrogenase/reductase SDR family member 7 (DHRS7) increases the reduction of 1,2-NAPHTHOQUINONE. [17]
1H-Indole-2,3-dione DMOZ91H Investigative Dehydrogenase/reductase SDR family member 7 (DHRS7) increases the reduction of 1H-Indole-2,3-dione. [17]
Nitrobenzaldehyde DM4UHB5 Investigative Dehydrogenase/reductase SDR family member 7 (DHRS7) increases the reduction of Nitrobenzaldehyde. [17]
BENZIL DM5Y2M8 Investigative Dehydrogenase/reductase SDR family member 7 (DHRS7) increases the reduction of BENZIL. [17]
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⏷ Show the Full List of 12 Drug(s)
2 Drug(s) Affected the Post-Translational Modifications of This DOT
Drug Name Drug ID Highest Status Interaction REF
Valproate DMCFE9I Approved Valproate decreases the methylation of Dehydrogenase/reductase SDR family member 7 (DHRS7). [1]
Benzo(a)pyrene DMN7J43 Phase 1 Benzo(a)pyrene affects the methylation of Dehydrogenase/reductase SDR family member 7 (DHRS7). [11]
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14 Drug(s) Affected the Gene/Protein Processing of This DOT
Drug Name Drug ID Highest Status Interaction REF
Ciclosporin DMAZJFX Approved Ciclosporin increases the expression of Dehydrogenase/reductase SDR family member 7 (DHRS7). [2]
Doxorubicin DMVP5YE Approved Doxorubicin increases the expression of Dehydrogenase/reductase SDR family member 7 (DHRS7). [3]
Cupric Sulfate DMP0NFQ Approved Cupric Sulfate decreases the expression of Dehydrogenase/reductase SDR family member 7 (DHRS7). [4]
Cisplatin DMRHGI9 Approved Cisplatin increases the expression of Dehydrogenase/reductase SDR family member 7 (DHRS7). [5]
Ivermectin DMDBX5F Approved Ivermectin decreases the expression of Dehydrogenase/reductase SDR family member 7 (DHRS7). [6]
Quercetin DM3NC4M Approved Quercetin increases the expression of Dehydrogenase/reductase SDR family member 7 (DHRS7). [7]
Temozolomide DMKECZD Approved Temozolomide decreases the expression of Dehydrogenase/reductase SDR family member 7 (DHRS7). [8]
Arsenic trioxide DM61TA4 Approved Arsenic trioxide increases the expression of Dehydrogenase/reductase SDR family member 7 (DHRS7). [9]
Amphotericin B DMTAJQE Approved Amphotericin B decreases the expression of Dehydrogenase/reductase SDR family member 7 (DHRS7). [10]
Bisphenol A DM2ZLD7 Investigative Bisphenol A increases the expression of Dehydrogenase/reductase SDR family member 7 (DHRS7). [12]
Milchsaure DM462BT Investigative Milchsaure decreases the expression of Dehydrogenase/reductase SDR family member 7 (DHRS7). [13]
Coumestrol DM40TBU Investigative Coumestrol decreases the expression of Dehydrogenase/reductase SDR family member 7 (DHRS7). [14]
chloropicrin DMSGBQA Investigative chloropicrin decreases the expression of Dehydrogenase/reductase SDR family member 7 (DHRS7). [15]
Deguelin DMXT7WG Investigative Deguelin increases the expression of Dehydrogenase/reductase SDR family member 7 (DHRS7). [16]
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⏷ Show the Full List of 14 Drug(s)

References

1 Integrative omics data analyses of repeated dose toxicity of valproic acid in vitro reveal new mechanisms of steatosis induction. Toxicology. 2018 Jan 15;393:160-170.
2 Integrating multiple omics to unravel mechanisms of Cyclosporin A induced hepatotoxicity in vitro. Toxicol In Vitro. 2015 Apr;29(3):489-501.
3 Bringing in vitro analysis closer to in vivo: studying doxorubicin toxicity and associated mechanisms in 3D human microtissues with PBPK-based dose modelling. Toxicol Lett. 2018 Sep 15;294:184-192.
4 Physiological and toxicological transcriptome changes in HepG2 cells exposed to copper. Physiol Genomics. 2009 Aug 7;38(3):386-401.
5 Activation of AIFM2 enhances apoptosis of human lung cancer cells undergoing toxicological stress. Toxicol Lett. 2016 Sep 6;258:227-236.
6 Quantitative proteomics reveals a broad-spectrum antiviral property of ivermectin, benefiting for COVID-19 treatment. J Cell Physiol. 2021 Apr;236(4):2959-2975. doi: 10.1002/jcp.30055. Epub 2020 Sep 22.
7 Comparison of phenotypic and transcriptomic effects of false-positive genotoxins, true genotoxins and non-genotoxins using HepG2 cells. Mutagenesis. 2011 Sep;26(5):593-604.
8 Temozolomide induces activation of Wnt/-catenin signaling in glioma cells via PI3K/Akt pathway: implications in glioma therapy. Cell Biol Toxicol. 2020 Jun;36(3):273-278. doi: 10.1007/s10565-019-09502-7. Epub 2019 Nov 22.
9 Gene expression profile induced by arsenic trioxide in chronic lymphocytic leukemia cells reveals a central role for heme oxygenase-1 in apoptosis and regulation of matrix metalloproteinase-9. Oncotarget. 2016 Dec 13;7(50):83359-83377.
10 Differential expression of microRNAs and their predicted targets in renal cells exposed to amphotericin B and its complex with copper (II) ions. Toxicol Mech Methods. 2017 Sep;27(7):537-543. doi: 10.1080/15376516.2017.1333554. Epub 2017 Jun 8.
11 Air pollution and DNA methylation alterations in lung cancer: A systematic and comparative study. Oncotarget. 2017 Jan 3;8(1):1369-1391. doi: 10.18632/oncotarget.13622.
12 Alternatives for the worse: Molecular insights into adverse effects of bisphenol a and substitutes during human adipocyte differentiation. Environ Int. 2021 Nov;156:106730. doi: 10.1016/j.envint.2021.106730. Epub 2021 Jun 27.
13 Transcriptional profiling of lactic acid treated reconstructed human epidermis reveals pathways underlying stinging and itch. Toxicol In Vitro. 2019 Jun;57:164-173.
14 Pleiotropic combinatorial transcriptomes of human breast cancer cells exposed to mixtures of dietary phytoestrogens. Food Chem Toxicol. 2009 Apr;47(4):787-95.
15 Transcriptomic analysis of human primary bronchial epithelial cells after chloropicrin treatment. Chem Res Toxicol. 2015 Oct 19;28(10):1926-35.
16 Neurotoxicity and underlying cellular changes of 21 mitochondrial respiratory chain inhibitors. Arch Toxicol. 2021 Feb;95(2):591-615. doi: 10.1007/s00204-020-02970-5. Epub 2021 Jan 29.
17 Biochemical properties of human dehydrogenase/reductase (SDR family) member 7. Chem Biol Interact. 2014 Jan 25;207:52-7. doi: 10.1016/j.cbi.2013.11.003. Epub 2013 Nov 16.