BDBM50368352 Cerubidine::DAUNORUBICIN
SMILES COc1cccc2C(=O)c3c(O)c4C[C@](O)(C[C@H](O[C@H]5C[C@H](N)[C@H](O)[C@H](C)O5)c4c(O)c3C(=O)c12)C(C)=O
InChI Key InChIKey=STQGQHZAVUOBTE-VGBVRHCVSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 14 hits for monomerid = 50368352
TargetMultidrug resistance-associated protein 1(Human)
University of Texas M. D. Anderson Cancer Center
Curated by ChEMBL
University of Texas M. D. Anderson Cancer Center
Curated by ChEMBL
Affinity DataKi: 70nMAssay Description:TP_TRANSPORTER: inhibition of LTC4 uptake in membrane vesicles from SR3A cellsMore data for this Ligand-Target Pair
TargetMultidrug resistance-associated protein 1(Human)
University of Texas M. D. Anderson Cancer Center
Curated by ChEMBL
University of Texas M. D. Anderson Cancer Center
Curated by ChEMBL
Affinity DataKi: 950nMAssay Description:TP_TRANSPORTER: inhibition of DNP-SG uptake in membrane vesicles from GLC4/ADR cellsMore data for this Ligand-Target Pair
Affinity DataKi: 2.50E+3nMAssay Description:TP_TRANSPORTER: inhibition of Taxol transepithelial transport (basal to apical) in Caco-2 cellsMore data for this Ligand-Target Pair
Affinity DataKi: 4.94E+4nMAssay Description:TP_TRANSPORTER: inhibition of Vinblastine transepithelial transport (basal to apical) in MRP2-expressing MDCK cellsMore data for this Ligand-Target Pair
Affinity DataKi: 1.11E+5nMAssay Description:TP_TRANSPORTER: inhibition of Digoxin transepithelial transport (basal to apical) in MDR1-expressing MDCK cellsMore data for this Ligand-Target Pair
TargetHistone deacetylase 8(Human)
National Institute of Pharmaceutical Education and Research (NIPER)
Curated by ChEMBL
National Institute of Pharmaceutical Education and Research (NIPER)
Curated by ChEMBL
Affinity DataIC50: 220nMAssay Description:Inhibition of HDAC8 (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 1.90E+3nMAssay Description:Inhibitory concentration against Clostridium histolyticum CollagenaseMore data for this Ligand-Target Pair
Affinity DataIC50: 2.36E+5nMAssay Description:Inhibition of HIV1 recombinant reverse transcriptase p66/p51 expressed in Escherichia coliMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of acid-mediated aggregation of TTR V30M mutant (unknown origin) expressed in Escherichia coli pretreated for 30 mins at pH 7 followed by ...More data for this Ligand-Target Pair
TargetHistone deacetylase 1(Human)
National Institute of Pharmaceutical Education and Research (NIPER)
Curated by ChEMBL
National Institute of Pharmaceutical Education and Research (NIPER)
Curated by ChEMBL
Affinity DataIC50: 47nMAssay Description:Inhibition of HDAC1 (unknown origin)More data for this Ligand-Target Pair
TargetHistone deacetylase 6(Human)
National Institute of Pharmaceutical Education and Research (NIPER)
Curated by ChEMBL
National Institute of Pharmaceutical Education and Research (NIPER)
Curated by ChEMBL
Affinity DataIC50: 20nMAssay Description:Inhibition of HDAC6 (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 2.36E+5nMAssay Description:Inhibition of HIV1 RTMore data for this Ligand-Target Pair
TargetMultidrug resistance-associated protein 1(Human)
University of Texas M. D. Anderson Cancer Center
Curated by ChEMBL
University of Texas M. D. Anderson Cancer Center
Curated by ChEMBL
Affinity DataIC50: 8.00E+3nMAssay Description:TP_TRANSPORTER: inhibition of E217betaG uptake (E217betaG: 0.05 uM) in membrane vesicle from MRP1-expressing HeLa cellsMore data for this Ligand-Target Pair
Affinity DataIC50: 1.39E+5nMAssay Description:Inhibition of HIV-1 reverse transcriptase using Poly(rA).p(dT) (12 to 18) as substrate after 30 mins by single point PCR assayMore data for this Ligand-Target Pair