aftin-4: increases production of amyloid-beta protein (1-42)
ID Source | ID |
---|---|
PubMed CID | 5289296 |
CHEMBL ID | 1235702 |
SCHEMBL ID | 19111944 |
MeSH ID | M0582982 |
Synonym |
---|
CHEMBL1235702 |
(2r)-2-({6-[benzyl(methyl)amino]-9-isopropyl-9h-purin-2-yl}amino)butan-1-ol |
(2r)-2-({6-[benzyl(methyl)amino]-9-isopropyl-9h-purin-2-yl}amino)-1-butanol |
n6-methyl-(r)-roscovitine |
bdbm10909 |
DB04776 |
(2r)-2-({6-[benzyl(methyl)amino]-9-(propan-2-yl)-9h-purin-2-yl}amino)butan-1-ol |
aftin-4 |
r-2-[6-(benzyl-methyl-amino)-9-isopropyl-9h-purin-2-ylamino]-butan-1-ol |
(2r)-2-[[6-[benzyl(methyl)amino]-9-propan-2-ylpurin-2-yl]amino]butan-1-ol |
866893-90-5 |
CS-0034791 |
HY-111267 |
(r)-2-((6-(benzyl(methyl)amino)-9-isopropyl-9h-purin-2-yl)amino)butan-1-ol |
(2r)-2-({6-[benzyl(methyl)amino]-9-(1-methylethyl)-9h-purin-2-yl}amino)butan-1-ol |
BCP29117 |
SCHEMBL19111944 |
aftin 4 |
AFTIN4 , |
BS-18191 |
Q27095514 |
C76827 |
1-butanol,2-[[9-(1-methylethyl)-6-[methyl(phenylmethyl)amino]-9h-purin-2-yl]amino]-, (2r)- |
EX-A4242 |
AKOS037649399 |
Protein | Taxonomy | Measurement | Average | Min (ref.) | Avg (ref.) | Max (ref.) | Bioassay(s) |
---|---|---|---|---|---|---|---|
G2/mitotic-specific cyclin-B | Marthasterias glacialis (spiny starfish) | IC50 (µMol) | 556.6667 | 0.0040 | 2.1093 | 9.4000 | AID1796565 |
G1/S-specific cyclin-E1 | Homo sapiens (human) | IC50 (µMol) | 556.6667 | 0.0010 | 1.0404 | 10.0000 | AID1796565 |
Cyclin-dependent kinase 2 | Homo sapiens (human) | IC50 (µMol) | 556.6667 | 0.0004 | 1.0444 | 10.0000 | AID1796565 |
Mitogen-activated protein kinase 1 | Homo sapiens (human) | IC50 (µMol) | 556.6667 | 0.0003 | 1.6878 | 9.2000 | AID1796565 |
Casein kinase I isoform alpha | Rattus norvegicus (Norway rat) | IC50 (µMol) | 556.6667 | 0.1600 | 1.0450 | 3.0000 | AID1796565 |
Cyclin-dependent-like kinase 5 | Homo sapiens (human) | IC50 (µMol) | 556.6667 | 0.0002 | 1.1832 | 10.0000 | AID1796565 |
Dual specificity tyrosine-phosphorylation-regulated kinase 1A | Homo sapiens (human) | IC50 (µMol) | 556.6667 | 0.0031 | 0.7140 | 9.0120 | AID1796565 |
Cyclin-dependent kinase 5 activator 1 | Homo sapiens (human) | IC50 (µMol) | 556.6667 | 0.0010 | 1.2898 | 10.0000 | AID1796565 |
Cyclin-dependent kinase 1 | Oryzias latipes (Japanese medaka) | IC50 (µMol) | 556.6667 | 0.0040 | 2.1093 | 9.4000 | AID1796565 |
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023] |
Protein | Taxonomy | Measurement | Average | Min (ref.) | Avg (ref.) | Max (ref.) | Bioassay(s) |
---|---|---|---|---|---|---|---|
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023] |
Assay ID | Title | Year | Journal | Article |
---|---|---|---|---|
AID1796565 | Kinase Inhibition Assay from Article 10.1074/jbc.M500805200: \\Crystal structure of pyridoxal kinase in complex with roscovitine and derivatives.\\ | 2005 | The Journal of biological chemistry, Sep-02, Volume: 280, Issue:35 | Crystal structure of pyridoxal kinase in complex with roscovitine and derivatives. |
AID712278 | Agonist activity at N-type Cav2.2 channel expressed in tsA201 cell assessed as calcium current by whole-cell patch clamp method | 2012 | ACS medicinal chemistry letters, Dec-13, Volume: 3, Issue:12 | Synthesis and biological evaluation of a selective N- and p/q-type calcium channel agonist. |
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (20.00) | 29.6817 |
2010's | 4 (80.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
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 | 5 (100.00%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |