diamthazole: RN given refers to parent cpd; structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]
| ID Source | ID |
|---|---|
| PubMed CID | 8708 |
| CHEMBL ID | 1184360 |
| CHEBI ID | 103934 |
| SCHEMBL ID | 467444 |
| MeSH ID | M0045880 |
| Synonym |
|---|
| HMS1473K01 |
| OPREA1_308992 |
| asterol |
| OPREA1_588999 |
| IDI1_019539 |
| CHEMDIV3_000221 |
| 7162-33-6 |
| 6-(2-diethylaminoethyloxy)-n,n-dimethyl-1,3-benzothiazol-2-amine |
| benzothiazole, 6-(2-diethyl-aminoethoxy)-2-dimethylamino- |
| NCGC00160485-01 |
| dimazole , |
| EC-000.1451 |
| 95-27-2 |
| NCGC00160485-02 |
| diamthazole |
| AKOS001483000 |
| BRD-K03978601-300-01-6 |
| 6-[2-(diethylamino)ethoxy]-n,n-dimethyl-1,3-benzothiazol-2-amine |
| CHEBI:103934 |
| 2-benzothiazolamine, 6-[2-(diethylamino)ethoxy]-n,n-dimethyl- |
| unii-2kl01r8zv1 |
| dimazole [inn] |
| einecs 202-406-5 |
| 2kl01r8zv1 , |
| diamethazole |
| dimazolo |
| 2-benzothiazolamine, 6-(2-(diethylamino)ethoxy)-n,n-dimethyl- |
| 6-(2-diethylaminoethoxy)-2-dimethylaminobenzothiazole |
| dimazolum [inn-latin] |
| diamthazole [inn:ban] |
| dimazolo [dcit] |
| dimazol [inn-spanish, french] |
| dimazol |
| 6-(2-diethylaminoethoxy)-2-dimethylaminobenzothiazol |
| dimazolum |
| 6-(2-diethylaminoethylaminoethoxy)-2-dimethylaminobenzothiazole |
| dtxsid1046182 , |
| cas-95-27-2 |
| dtxcid9026182 |
| tox21_111847 |
| STK525110 |
| CHEMBL1184360 |
| CCG-103023 |
| dimazole [who-dd] |
| SCHEMBL467444 |
| WGMYEOIMVYADRJ-UHFFFAOYSA-N |
| 6-[2-(diethylamino)ethoxy]-n,n-dimethyl-1,3-benzothiazol-2-amine # |
| 6-(2-diethylaminoethoxy)-n,n-dimethyl-1,3-benzothiazol-2-amine |
| Q5277172 |
| 6-(2-(diethylamino)ethoxy)-n,n-dimethylbenzo[d]thiazol-2-amine |
| DB13858 |
| EN300-18560030 |
| CS-0613910 |
| HY-148160 |
| Excerpt | Reference | Relevance |
|---|---|---|
| "The ATP-binding cassette transporter P-glycoprotein (P-gp) is known to limit both brain penetration and oral bioavailability of many chemotherapy drugs." | ( A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein. Ambudkar, SV; Brimacombe, KR; Chen, L; Gottesman, MM; Guha, R; Hall, MD; Klumpp-Thomas, C; Lee, OW; Lee, TD; Lusvarghi, S; Robey, RW; Shen, M; Tebase, BG, 2019) | 0.51 |
| Class | Description |
|---|---|
| benzothiazoles | |
| [compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res] | |
| Protein | Taxonomy | Measurement | Average (µ) | Min (ref.) | Avg (ref.) | Max (ref.) | Bioassay(s) |
|---|---|---|---|---|---|---|---|
| TDP1 protein | Homo sapiens (human) | Potency | 8.5473 | 0.0008 | 11.3822 | 44.6684 | AID686978; AID686979 |
| AR protein | Homo sapiens (human) | Potency | 13.7282 | 0.0002 | 21.2231 | 8,912.5098 | AID743042; AID743054 |
| pregnane X nuclear receptor | Homo sapiens (human) | Potency | 17.7828 | 0.0054 | 28.0263 | 1,258.9301 | AID1346985 |
| estrogen nuclear receptor alpha | Homo sapiens (human) | Potency | 24.0906 | 0.0002 | 29.3054 | 16,493.5996 | AID743079; AID743080; AID743091 |
| aryl hydrocarbon receptor | Homo sapiens (human) | Potency | 19.9682 | 0.0007 | 23.0674 | 1,258.9301 | AID743085; AID743122 |
| cytochrome P450, family 19, subfamily A, polypeptide 1, isoform CRA_a | Homo sapiens (human) | Potency | 29.8493 | 0.0017 | 23.8393 | 78.1014 | AID743083 |
| peripheral myelin protein 22 | Rattus norvegicus (Norway rat) | Potency | 36.1254 | 0.0056 | 12.3677 | 36.1254 | AID624032 |
| lamin isoform A-delta10 | Homo sapiens (human) | Potency | 1.4125 | 0.8913 | 12.0676 | 28.1838 | AID1487 |
| Cellular tumor antigen p53 | Homo sapiens (human) | Potency | 13.3332 | 0.0023 | 19.5956 | 74.0614 | AID651631 |
| Spike glycoprotein | Severe acute respiratory syndrome-related coronavirus | Potency | 15.8489 | 0.0096 | 10.5250 | 35.4813 | AID1479145 |
| [prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023] | |||||||
| Assay ID | Title | Year | Journal | Article |
|---|---|---|---|---|
| AID504749 | qHTS profiling for inhibitors of Plasmodium falciparum proliferation | 2011 | Science (New York, N.Y.), Aug-05, Volume: 333, Issue:6043 | Chemical genomic profiling for antimalarial therapies, response signatures, and molecular targets. |
| AID1346986 | P-glycoprotein substrates identified in KB-3-1 adenocarcinoma cell line, qHTS therapeutic library screen | 2019 | Molecular pharmacology, 11, Volume: 96, Issue:5 | A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein. |
| AID1296008 | Cytotoxic Profiling of Annotated Libraries Using Quantitative High-Throughput Screening | 2020 | SLAS discovery : advancing life sciences R & D, 01, Volume: 25, Issue:1 | Cytotoxic Profiling of Annotated and Diverse Chemical Libraries Using Quantitative High-Throughput Screening. |
| AID1346987 | P-glycoprotein substrates identified in KB-8-5-11 adenocarcinoma cell line, qHTS therapeutic library screen | 2019 | Molecular pharmacology, 11, Volume: 96, Issue:5 | A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein. |
| AID588519 | A screen for compounds that inhibit viral RNA polymerase binding and polymerization activities | 2011 | Antiviral research, Sep, Volume: 91, Issue:3 | High-throughput screening identification of poliovirus RNA-dependent RNA polymerase inhibitors. |
| AID540299 | A screen for compounds that inhibit the MenB enzyme of Mycobacterium tuberculosis | 2010 | Bioorganic & medicinal chemistry letters, Nov-01, Volume: 20, Issue:21 | Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis. |
| [information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] | ||||
| Timeframe | Studies, This Drug (%) | All Drugs % |
|---|---|---|
| pre-1990 | 15 (75.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 4 (20.00) | 24.3611 |
| 2020's | 1 (5.00) | 2.80 |
| [information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] | ||
According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be moderate demand-to-supply ratio for research on this compound.
| This Compound (17.07) All Compounds (24.57) |
| Publication Type | This drug (%) | All Drugs (%) |
|---|---|---|
| Trials | 0 (0.00%) | 5.53% |
| Reviews | 0 (0.00%) | 6.00% |
| Case Studies | 0 (0.00%) | 4.05% |
| Observational | 0 (0.00%) | 0.25% |
| Other | 21 (100.00%) | 84.16% |
| [information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] | ||