N,N-dimethylaminoisopropanol: RN given refers to parent cpd without isomeric designation
ID Source | ID |
---|---|
PubMed CID | 37511 |
CHEMBL ID | 3186209 |
SCHEMBL ID | 8389 |
MeSH ID | M0099734 |
Synonym |
---|
108-16-7 |
nsc-3163 |
n,n-(dimethylamino)-2-propanol |
dimethylisopropanolamine |
2-propanol,1-(dimethylamino)- |
wln: qy1 & 1n1 & 1 |
nsc3163 |
n,n-dimethyl-2-hydroxypropylamine |
dimethyl(2-hydroxypropyl)amine |
1,1-(dimethylamino)propanol-2 |
1-(dimethylamino)-2-propanol |
n,n-dimethylisopropanolamine |
2-propanol, 1-(dimethylamino)- |
dimepranol [inn] |
einecs 203-556-4 |
ai3-18202 |
2-propanol, 1,1-(dimethylamino)- |
nsc 3163 |
brn 1209244 |
n,n-dimethylaminoisopropanol |
1,1-dimethylaminopropanol-2 |
dimepranolum [inn-latin] |
1-(dimethylamino)propan-2-ol |
1-dimethylamino-2-propanol, >=99% |
NCGC00166041-01 |
dimepranol |
1-dimethylamino-2-propanol |
D0660 |
dtxsid5031210 , |
tox21_112297 |
dtxcid3011210 |
cas-108-16-7 |
AKOS005206825 |
4-04-00-01666 (beilstein handbook reference) |
unii-ox17195h4t |
ec 203-556-4 |
ox17195h4t , |
dimepranolum |
FT-0640183 |
FT-0605825 |
1-dimethylamino-propan-2-ol |
1-dimethylaminopropan-2-ol |
1-(n,n-dimethylamino)-2-propanol |
1-dimethyamino-2-propanol |
racemic 1-dimethylamino-2-propanol |
SCHEMBL8389 |
dimethyl isopropanolamine |
(+/-)-1-(n,n-dimethylamino)-2-propanol |
n,n-dimethylamino-2-propanol |
1-methyl-2-(dimethylamino)ethanol |
n,n-dimethyl-2-hydroxy-1-propanamine |
dimethyl isopropanolamine [inci] |
2-(dimethylamino)-1-methylethanol |
dl-1-(dimethylamino)-2-propanol |
3-(dimethylamino)-2-propanol |
dma-2p |
2-propanol, 1-(dimethylamino)-, (+/-)- |
extendex 50 |
2-(dimethylamino)-1-methyl-1-ethanol |
(+/-)-1-(dimethylamino)-2-propanol |
3-dimethylamino-2-propanol |
1,1-dimethylaminopropan-2-ol |
W-108726 |
CHEMBL3186209 |
mfcd00004532 |
SR-01000944920-1 |
sr-01000944920 |
1-dimethylamino-2-propanol, 99% |
Q26841310 |
AMY13331 |
SB74230 |
SB46768 |
BS-22423 |
1-dimethylamino-2-propanol(dimepranol) |
2-propanol, 1-[di(methyl-d3)amino]- |
mfcd00065951 |
(r)-1-(dimethylamino)-2-propanol |
SY164931 |
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 |
Excerpt | Relevance | Reference |
---|---|---|
" This metabolite accounted for 50% of the administered dose in orally dosed animals and 31% in iv dosed animals." | ( Inosiplex: metabolism and excretion of the dimethylaminoisopropanol and p-acetamidobenzoic acid components in rhesus monkeys. Pfadenhauer, EH; Streeter, DG, ) | 0.13 |
Protein | Taxonomy | Measurement | Average (µ) | Min (ref.) | Avg (ref.) | Max (ref.) | Bioassay(s) |
---|---|---|---|---|---|---|---|
estrogen nuclear receptor alpha | Homo sapiens (human) | Potency | 16.5880 | 0.0002 | 29.3054 | 16,493.5996 | AID743075; AID743079 |
[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. |
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. |
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. |
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. |
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 1 (14.29) | 18.7374 |
1990's | 1 (14.29) | 18.2507 |
2000's | 2 (28.57) | 29.6817 |
2010's | 2 (28.57) | 24.3611 |
2020's | 1 (14.29) | 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 weak demand-to-supply ratio for research on this compound.
| This Compound (12.57) 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 | 8 (100.00%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |