3-(N-benzylsulfamoyl)-4-bromo-N-(4-bromophenyl)benzamide: stimulates RAD51 DNA-binding activity to promote cancer cell death; structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]
ID Source | ID |
---|---|
PubMed CID | 1039737 |
CHEMBL ID | 1598912 |
SCHEMBL ID | 13186460 |
MeSH ID | M000598928 |
Synonym |
---|
EU-0034229 |
NCGC00141035-01 |
OPREA1_698256 |
OPREA1_166111 |
RS1 , |
HMS1917E02 |
AKOS000731000 |
3-(benzylsulfamoyl)-4-bromo-n-(4-bromophenyl)benzamide |
STL170129 |
3-[(benzylamino)sulfonyl]-4-bromo-n-(4-bromophenyl)benzamide |
rs-1 |
312756-74-4 |
rad51-stimulatory compound-1, rs-1 |
S8234 |
CHEMBL1598912 |
SCHEMBL13186460 |
4-bromo-n-(4-bromophenyl)-3-[[(phenylmethyl)amino]sulfonyl]benzamide |
AC-35367 |
3-(n-benzylsulfamoyl)-4-bromo-n-(4-bromophenyl)benzamide |
HY-19793 |
sr-01000395441 |
SR-01000395441-1 |
EX-A1010 |
DTXSID80359902 |
CS-5642 |
rad51-stimulatory compound-1 |
benzamide, 4-bromo-n-(4-bromophenyl)-3-[[(phenylmethyl)amino]sulfonyl]- |
rs-1, >=98% (hplc) |
J-018355 |
mfcd00348720 |
A16153 |
BCP18095 |
c20h16n2o3sbr2 |
HB5647 |
4-bromanyl-n-(4-bromophenyl)-3-[(phenylmethyl)sulfamoyl]benzamide |
J46 , |
CP-0069 |
CCG-96390 |
A912272 |
4-bromo-n-(4-bromophenyl)-3-(((phenylmethyl)amino)sulfonyl)benzamide |
R0215 |
Z275140708 |
Protein | Taxonomy | Measurement | Average (µ) | Min (ref.) | Avg (ref.) | Max (ref.) | Bioassay(s) |
---|---|---|---|---|---|---|---|
Chain A, Cruzipain | Trypanosoma cruzi | Potency | 39.8107 | 0.0020 | 14.6779 | 39.8107 | AID1476 |
glp-1 receptor, partial | Homo sapiens (human) | Potency | 10.0000 | 0.0184 | 6.8060 | 14.1254 | AID624417 |
Microtubule-associated protein tau | Homo sapiens (human) | Potency | 12.5893 | 0.1800 | 13.5574 | 39.8107 | AID1468 |
Smad3 | Homo sapiens (human) | Potency | 12.5893 | 0.0052 | 7.8098 | 29.0929 | AID588855 |
PINK1 | Homo sapiens (human) | Potency | 50.1187 | 2.8184 | 18.8959 | 44.6684 | AID624263 |
67.9K protein | Vaccinia virus | Potency | 28.1838 | 0.0001 | 8.4406 | 100.0000 | AID720579 |
Parkin | Homo sapiens (human) | Potency | 50.1187 | 0.8199 | 14.8306 | 44.6684 | AID624263 |
cellular tumor antigen p53 isoform a | Homo sapiens (human) | Potency | 15.6739 | 0.3162 | 12.4435 | 31.6228 | AID902; AID903; AID924 |
parathyroid hormone/parathyroid hormone-related peptide receptor precursor | Homo sapiens (human) | Potency | 31.6228 | 3.5481 | 19.5427 | 44.6684 | AID743266 |
Integrin beta-3 | Homo sapiens (human) | Potency | 11.2202 | 0.3162 | 11.4157 | 31.6228 | AID924 |
Integrin alpha-IIb | Homo sapiens (human) | Potency | 11.2202 | 0.3162 | 11.4157 | 31.6228 | AID924 |
Alpha-synuclein | Homo sapiens (human) | Potency | 0.5623 | 0.5623 | 9.3985 | 25.1189 | AID652106 |
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023] |
Assay ID | Title | Year | Journal | Article |
---|---|---|---|---|
AID651635 | Viability Counterscreen for Primary qHTS for Inhibitors of ATXN expression | |||
AID1745845 | Primary qHTS for Inhibitors of ATXN expression | |||
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. |
AID1178406 | Induction of RAD51 in cisplatin-treated neonatal human skin fibroblast assessed as increase in survival at 7.5 uM relative to untreated control | 2014 | Bioorganic & medicinal chemistry letters, Jul-15, Volume: 24, Issue:14 | Targeting the homologous recombination pathway by small molecule modulators. |
[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 | 3 (60.00) | 24.3611 |
2020's | 1 (20.00) | 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 weak demand-to-supply ratio for research on this compound.
| This Compound (13.13) All Compounds (24.57) |
Publication Type | This drug (%) | All Drugs (%) |
---|---|---|
Trials | 0 (0.00%) | 5.53% |
Reviews | 1 (20.00%) | 6.00% |
Case Studies | 0 (0.00%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 4 (80.00%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |