ID Source | ID |
---|---|
PubMed CID | 10256643 |
CHEMBL ID | 537419 |
MeSH ID | M0169943 |
Synonym |
---|
MLS002153401 |
cgs 21680 (hydrochloride) |
HY-13201A |
REGID_FOR_CID_10256643 |
MLS001056776 |
smr000058796 |
cgs 21680 hydrochloride |
2-p-(2-carboxyethyl)phenethylamino-5'-n-ethylcarboxamidoadenosine hydrochloride |
3-{4-[2-({6-amino-9-[(2r,3r,4s,5s)-5-(ethylcarbamoyl)-3,4-dihydroxytetrahydrofuran-2-yl]-9h-purin-2-yl}amino)ethyl]phenyl}propanoic acid hydrochloride |
cgs 21680a |
124431-80-7 |
hydrochloride salt of (2-(p-2-carboxyethyl)phenethylamino)-5'-n-ethylcarboxamidoadenosine |
benzenepropanoic acid, 4-(2-((6-amino-9-(n-ethyl-beta-d-ribofuranuronamidosyl)-9h-purin-2-yl)amino)ethyl)-, monohydrochloride |
CHEMBL537419 |
BCP9000512 |
3-(4-(2-(6-amino-9-((2r,3r,4s,5s)-5-(ethylcarbamoyl)-3,4-dihydroxytetrahydrofuran-2-yl)-9h-purin-2-ylamino)ethyl)phenyl)propanoic acid hydrochloride |
CS-0425 |
S2153 , |
MLS006011122 |
4-[2-[[6-amino-9-(n-ethyl-?-d-ribofuranuronamidosyl)-9h-purin-2-yl]amino]ethyl]benzenepropanoic acid hydrochloride |
AC-32733 |
AKOS024456361 |
3-(4-(2-((6-amino-9-((2r,3r,4s,5s)-5-(ethylcarbamoyl)-3,4-dihydroxytetrahydrofuran-2-yl)-9h-purin-2-yl)amino)ethyl)phenyl)propanoic acid hydrochloride |
cgs 21680 hcl |
DTXSID2040999 |
mfcd00078573 |
J-005077 |
AS-75112 |
3-{4-[2-({6-amino-9-[(2r,3r,4s,5s)-5-(ethylcarbamoyl)-3,4-dihydroxyoxolan-2-yl]-9h-purin-2-yl}amino)ethyl]phenyl}propanoic acid hydrochloride |
3-[4-[2-[[6-amino-9-[(2r,3r,4s,5s)-5-(ethylcarbamoyl)-3,4-dihydroxyoxolan-2-yl]purin-2-yl]amino]ethyl]phenyl]propanoic acid;hydrochloride |
3-(4-(2-((6-amino-9-((2r,3r,4s,5s)-5-(ethylcarbamoyl)-3,4-dihydroxytetrahydro-furan-2-yl)-9h-purin-2-yl)amino)ethyl)phenyl)propanoic acid hydrochloride |
EX-A2473 |
cgs21680 hcl |
cgs21680hydrochloride |
benzenepropanoic acid, 4-[2-[[6-amino-9-(n-ethyl-beta-d-ribofuranuronamidosyl)-9h-purin-2-yl]amino]ethyl]-, hydrochloride (1:1) |
CCG-269942 |
Protein | Taxonomy | Measurement | Average (mM) | Bioassay(s) |
---|---|---|---|---|
Chain A, 2-oxoglutarate Oxygenase | Homo sapiens (human) | Potency | 28.1838 | AID2147 |
glp-1 receptor, partial | Homo sapiens (human) | Potency | 28.1838 | AID624417 |
serine-protein kinase ATM isoform a | Homo sapiens (human) | Potency | 39.8107 | AID485349 |
chromobox protein homolog 1 | Homo sapiens (human) | Potency | 112.2020 | AID540317 |
geminin | Homo sapiens (human) | Potency | 0.7079 | AID624297 |
Protein | Taxonomy | Measurement | Average (mM) | Bioassay(s) |
---|---|---|---|---|
high affinity choline transporter 1 isoform a | Homo sapiens (human) | IC50 | 0.8609 | AID504840; AID588401 |
Assay ID | Title | Year | Journal | Article |
---|---|---|---|---|
AID588499 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set | 2010 | Current protocols in cytometry, Oct, Volume: Chapter 13ISSN: 1934-9300 | Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening. |
AID588499 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set | 2006 | Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5 ISSN: 1552-4922 | Microsphere-based protease assays and screening application for lethal factor and factor Xa. |
AID588499 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set | 2010 | Assay and drug development technologies, Feb, Volume: 8, Issue:1 ISSN: 1557-8127 | High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors. |
AID588501 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set | 2010 | Current protocols in cytometry, Oct, Volume: Chapter 13ISSN: 1934-9300 | Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening. |
AID588501 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set | 2006 | Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5 ISSN: 1552-4922 | Microsphere-based protease assays and screening application for lethal factor and factor Xa. |
AID588501 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set | 2010 | Assay and drug development technologies, Feb, Volume: 8, Issue:1 ISSN: 1557-8127 | High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors. |
AID588497 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set | 2010 | Current protocols in cytometry, Oct, Volume: Chapter 13ISSN: 1934-9300 | Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening. |
AID588497 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set | 2006 | Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5 ISSN: 1552-4922 | Microsphere-based protease assays and screening application for lethal factor and factor Xa. |
AID588497 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set | 2010 | Assay and drug development technologies, Feb, Volume: 8, Issue:1 ISSN: 1557-8127 | High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors. |
AID651635 | Viability Counterscreen for Primary qHTS for Inhibitors of ATXN expression | 2022 | The Journal of biological chemistry, 08, Volume: 298, Issue:8 ISSN: 1083-351X | |
AID1745845 | Primary qHTS for Inhibitors of ATXN expression | 2022 | The Journal of biological chemistry, 08, Volume: 298, Issue:8 ISSN: 1083-351X | |
AID504812 | Inverse Agonists of the Thyroid Stimulating Hormone Receptor: HTS campaign | 2010 | Endocrinology, Jul, Volume: 151, Issue:7 ISSN: 1945-7170 | A small molecule inverse agonist for the human thyroid-stimulating hormone receptor. |
AID504810 | Antagonists of the Thyroid Stimulating Hormone Receptor: HTS campaign | 2010 | Endocrinology, Jul, Volume: 151, Issue:7 ISSN: 1945-7170 | A small molecule inverse agonist for the human thyroid-stimulating hormone receptor. |
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 | 3 (60.00) | 24.3611 |
2020's | 1 (20.00) | 2.80 |
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% |
Condition | Indicated | Studies | First Year | Last Year | Average Age | Relationship Strength | Trials | pre-1990 | 1990's | 2000's | 2010's | post-2020 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
Inflammation | 0 | 2010 | 2010 | 14.0 | high | 0 | 0 | 0 | 1 | 0 | 0 | |
Innate Inflammatory Response | 0 | 2010 | 2010 | 14.0 | high | 0 | 0 | 0 | 1 | 0 | 0 |