In ZINC since | Heavy atoms | Benign functionality |
---|---|---|
October 26th, 2009 | 28 | No |
Popular Name: (E)-N-(2-aminophenyl)-3-[6-(3-phenylpropylamino)-3-pyridyl]prop-2-enamide (E)-N-(2-aminophenyl)-3-[6-(3-ph…
Type pH range | xlogP | Des A‑Pol Apolar desolvation (kcal/mol) | Des Pol Polar desolvation (kcal/mol) | H Don H-bond donors | H Acc H-bond acceptors | Chg Net charge | tPSA (Ų) | MWT Molecular weight (g/mol) | RB Rotatable bonds | DL |
---|---|---|---|---|---|---|---|---|---|---|
Ref Reference (pH 7) | 4.01 | 9.12 | -12.3 | 4 | 5 | 0 | 80 | 372.472 | 8 | ↓ |
Lo Low (pH 4.5-6) | 4.01 | 9.59 | -44.16 | 5 | 5 | 1 | 81 | 373.48 | 8 | ↓ |
Code | Description | Organism Class | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
HDAC1-2-E | Histone Deacetylase 1 (cluster #2 Of 4), Eukaryotic | Eukaryotes | 3000 | 0.28 | Binding ≤ 10μM |
Z80928-3-O | HCT-116 (Colon Carcinoma Cells) (cluster #3 Of 9), Other | Other | 2000 | 0.28 | Functional ≤ 10μM |
Uniprot | Swissprot | Description | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
HDAC1_HUMAN | Q13547 | Histone Deacetylase 1, Human | 3000 | 0.28 | Binding ≤ 10μM |
Z80928 | Z80928 | HCT-116 (Colon Carcinoma Cells) | 2000 | 0.28 | Functional ≤ 10μM |
Description | Species |
---|---|
Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants | |
Constitutive Signaling by NOTCH1 PEST Domain Mutants | |
deactivation of the beta-catenin transactivating complex | |
Downregulation of SMAD2/3:SMAD4 transcriptional activity | |
Factors involved in megakaryocyte development and platelet production | |
formation of the beta-catenin:TCF transactivating complex | |
G0 and Early G1 | |
HDACs deacetylate histones | |
NoRC negatively regulates rRNA expression | |
NOTCH1 Intracellular Domain Regulates Transcription | |
p75NTR negatively regulates cell cycle via SC1 | |
repression of WNT target genes | |
RNA Polymerase I Transcription Initiation | |
SMAD2/SMAD3:SMAD4 heterotrimer regulates transcription |
No pre-computed analogs available. Try a structural similarity search.