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Drug Details

General Information of the Drug (ID: DR9750)
Name
BRD4770
Synonyms
BRD4770; 1374601-40-7; Methyl 2-benzamido-1-(3-phenylpropyl)-1H-benzo[d]imidazole-5-carboxylate; BRD 4770; BRD-4770; methyl 2-benzamido-1-(3-phenylpropyl)benzimidazole-5-carboxylate; C25H23N3O3; GTPL7016; AOB3886; CHEMBL3970748; SCHEMBL16569005; EX-A692; CHEBI:131143; BDBM225263; BCP10433; 2282AH; MFCD23143627; NSC777671; s7591; ZINC95099914; AKOS026750266; BRD 4770;BRD-4770; CCG-268804; CS-3446; NSC-777671; SB19344; NCGC00351780-01; NCGC00351780-04; AS-16771; DA-35008; HY-16705; BRD4770, >=98% (HPLC); FT-0733814; A14401; J-690148; BRD-K72264770-001-01-6; Q27075478; methyl 2-benzamido-1-(3-phenylpropyl)-1H-1,3-benzodiazole-5-carboxylate; Methyl-2-(benzoylamino)-1-(3-phenylpropyl)-1H-benzimidazole-5-carboxylate; 2-(Benzoylamino)-1-(3-phenylpropyl)-1H-benzimidazole-5-carboxylic acid methyl ester
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Molecular Type
Small molecule
Disease Pancreatic cancer [ICD-11: 2C10] Investigative [1]
Structure
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2D MOL

3D MOL

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Formula
C25H23N3O3
PubChem CID
72193870
Canonical SMILES
COC(=O)C1=CC2=C(C=C1)N(C(=N2)NC(=O)C3=CC=CC=C3)CCCC4=CC=CC=C4
InChI
1S/C25H23N3O3/c1-31-24(30)20-14-15-22-21(17-20)26-25(27-23(29)19-12-6-3-7-13-19)28(22)16-8-11-18-9-4-2-5-10-18/h2-7,9-10,12-15,17H,8,11,16H2,1H3,(H,26,27,29)
InChIKey
UCGWYCMPZXDHNR-UHFFFAOYSA-N
ChEBI ID
CHEBI:131143
TTD Drug ID
D0LA0P
Combinatorial Therapeutic Effect(s) Validated Clinically or Experimentally
    α. A List of Natural Product(s) Able to Enhance the Efficacy of This Drug
          Gossypol      Gossypium herbaceum     Click to Show/Hide the Molecular Data of This NP
                 Achieving Therapeutic Synergy     Click to Show/Hide
                    Representative Experiment Reporting the Effect of This Combination [2]
                    Detail(s)  Combination Info  click to show the detail info of this combination
                    Molecule(s)
                    Regulation
Up-regulation Expression MAP1LC3A  Molecule Info 
Pathway MAP
                    Biological
                    Regulation
Increase Autophagosome formation
                    In-vitro Model MCF-7 CVCL_0031 Invasive breast carcinoma Homo sapiens
HPAC CVCL_3517 Pancreatic adenocarcinoma Homo sapiens
PANC-1 CVCL_0480 Pancreatic ductal adenocarcinoma Homo sapiens
HeLa CVCL_0030 Endocervical adenocarcinoma Homo sapiens
PC-3 CVCL_0035 Prostate carcinoma Homo sapiens
                    Experimental
                    Result(s)
The combination of gossypol and BRD4770 increased LC3-II levels and the autophagosome number in PANC-1 cells, and the compound combination appears to act in a BNIP3-dependent manner, suggesting that these compounds act together to induce autophagy-related cell death in pancreatic cancer cells.
References
Reference 1 A small-molecule probe of the histone methyltransferase G9a induces cellular senescence in pancreatic adenocarcinoma. ACS Chem Biol. 2012 Jul 20;7(7):1152-7.
Reference 2 Gossypol and an HMT G9a inhibitor act in synergy to induce cell death in pancreatic cancer cells. Cell Death Dis. 2013 Jun 27;4(6):e690.
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Cite NPCDR
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Correspondence

X. N. Sun, Y. T. Zhang, Y. Zhou, X. C. Lian, L. L. Yan, T. Pan, T. Jin, H. Xie, Z. M. Liang, W. Q. Qiu, J. X. Wang, Z. R. Li, F. Zhu*, X. B. Sui*. NPCDR: natural product-based drug combination and its disease-specific molecular regulation. Nucleic Acids Research. 50(D1): 1324-1333 (2020). PMID: 34664659

Prof. Feng ZHU  (zhufeng@zju.edu.cn)

College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, China


Prof. Xinbing SUI  (hzzju@hznu.edu.cn)

School of Pharmacy and Department of Medical Oncology, the Affiliated Hospital of Hangzhou Normal University, Hangzhou Normal University, Hangzhou, China