Skip to main content
  •   Home
  •   Download
  •   Manual
  •   Contact

Drug Details

General Information of the Drug (ID: DR7504)
Name
GW9662
Synonyms
GW9662; 22978-25-2; 2-Chloro-5-nitro-N-phenylbenzamide; GW 9662; 2-Chloro-5-nitrobenzanilide; GW-9662; benzamide, 2-chloro-5-nitro-N-phenyl-; UNII-UM18UZV2YD; MFCD01215270; UM18UZV2YD; MLS001056751; CHEBI:79993; 2-Chloro-5-nitro-N-phenyl-benzamide; 2-Chloro-5-nitro- N -phenylbenzamide; 2-Chloro-5-nitro-N-4-phenylbenzamide; SMR000326735; (2-chloro-5-nitrophenyl)-N-benzamide; SR-01000075999; Benzamide,2-chloro-5-nitro-N-phenyl-; Tocris-1508; Spectrum5_001989; Lopac-M-6191; DSSTox_CID_20723; DSSTox_RID_79570; DSSTox_GSID_40723; Lopac0_000798; BSPBio_001021; KBioGR_000361; KBioSS_000361; SCHEMBL420231; CHEMBL375270; cid_644213; GTPL3442; DTXSID8040723; BCBcMAP01_000086; BDBM55936; KBio2_000361; KBio2_002929; KBio2_005497; KBio3_000701; KBio3_000702; ZINC39173; EX-A595; Bio2_000341; Bio2_000821; HMS1362C03; HMS1792C03; HMS1990C03; HMS2235C11; HMS3262O18; HMS3267P20; HMS3372P17; HMS3403C03; HMS3412F15; HMS3649C18; HMS3651L10; HMS3676F15; AOB31774; BCP06354; 2-Chloro-5-nitrobenzanilide, 97%; METHYL15-METHYLHEPTADECANOATE; Tox21_301993; Tox21_500798; s2915; SBB006523; STL260137; AKOS000155195; CCG-204882; CS-1102; DB07863; LP00798; MCULE-8174475490; SDCCGSBI-0050775.P002; 2-chloranyl-5-nitro-N-phenyl-benzamide; IDI1_002096; Benzanilide, 2-chloro-5-nitro- (8CI); NCGC00015688-01; NCGC00015688-02; NCGC00015688-03; NCGC00015688-04; NCGC00015688-05; NCGC00015688-06; NCGC00015688-07; NCGC00015688-08; NCGC00015688-09; NCGC00015688-21; NCGC00025193-01; NCGC00025193-02; NCGC00025193-03; NCGC00025193-04; NCGC00025193-05; NCGC00025193-06; NCGC00025193-07; NCGC00255683-01; NCGC00261483-01; AC-31443; AK173264; AS-14069; GW9662, >98% (HPLC); HY-16578; ST055753; SY040458; AB0109180; CAS-22978-25-2; EU-0100798; FT-0664839; SW203813-2; Z6199; EC-000.2405; A11984; Benzamide, 2-chloro-5-nitro-N-phenyl- (9CI); C15627; J90030; M 6191; S-7731; J-014928; SR-01000075999-1; SR-01000075999-3; SR-01000075999-6; SR-01000075999-9; BRD-K93258693-001-02-5; BRD-K93258693-001-05-8; Q27077962; Z27782632
    Click to Show/Hide
Molecular Type
Small molecule
Disease Breast cancer [ICD-11: 2C60] Investigative [1]
Structure
Click to Download Mol
2D MOL

3D MOL

    Click to Show/Hide the Molecular Information and External Link(s) of This Natural Product
Formula
C13H9ClN2O3
PubChem CID
644213
Canonical SMILES
C1=CC=C(C=C1)NC(=O)C2=C(C=CC(=C2)[N+](=O)[O-])Cl
InChI
1S/C13H9ClN2O3/c14-12-7-6-10(16(18)19)8-11(12)13(17)15-9-4-2-1-3-5-9/h1-8H,(H,15,17)
InChIKey
DNTSIBUQMRRYIU-UHFFFAOYSA-N
CAS Number
CAS 22978-25-2
ChEBI ID
CHEBI:79993
TTD Drug ID
D00ACX
Combinatorial Therapeutic Effect(s) Validated Clinically or Experimentally
    α. A List of Natural Product(s) Able to Enhance the Efficacy of This Drug
          Gamma tocotrienol      Bixa orellana     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
Down-regulation Expression CCND1  Molecule Info 
Pathway MAP
Down-regulation Expression CDK4  Molecule Info 
Pathway MAP
Down-regulation Expression CDK6  Molecule Info 
Pathway MAP
Down-regulation Expression COX-2  Molecule Info 
Pathway MAP
Down-regulation Expression HPGDS  Molecule Info 
Pathway MAP
                    In-vitro Model MCF-7 CVCL_0031 Invasive breast carcinoma Homo sapiens
MDA-231 Breast cancer Homo sapiens
Neoplastic +SA cells derived from a mammary adenocarcinoma Mammary Adenocarcinoma Homo sapiens
                    Experimental
                    Result(s)
Combined Gamma -tocotrienol and PPAR Gamma antagonists treatment in PPAR Gamma negative/silenced breast cancer cells are mediated through PPAR Gamma -independent mechanisms that are associated with a downregulation in COX-2, PGDS, and PGD2 synthesis.
Target and Pathway
Target(s) PPAR-gamma (PPARG)  Molecule Info  [3]
Retinoic acid receptor RXR-alpha (RXRA)  Molecule Info  [3]
KEGG Pathway PPAR signaling pathway Click to Show/Hide
2 PI3K-Akt signaling pathway
3 Thyroid hormone signaling pathway
4 Adipocytokine signaling pathway
5 Non-alcoholic fatty liver disease (NAFLD)
6 Bile secretion
7 Hepatitis C
8 Pathways in cancer
9 Transcriptional misregulation in cancer
10 Thyroid cancer
11 Small cell lung cancer
12 Non-small cell lung cancer
13 AMPK signaling pathway
14 Osteoclast differentiation
15 Huntington's disease
NetPath Pathway IL1 Signaling Pathway Click to Show/Hide
2 TGF_beta_Receptor Signaling Pathway
3 Leptin Signaling Pathway
Panther Pathway Vitamin D metabolism and pathway Click to Show/Hide
2 CCKR signaling map ST
Pathway Interaction Database Regulation of Androgen receptor activity Click to Show/Hide
2 RXR and RAR heterodimerization with other nuclear receptor
3 Retinoic acid receptors-mediated signaling
4 a6b1 and a6b4 Integrin signaling
5 Noncanonical Wnt signaling pathway
6 Calcineurin-regulated NFAT-dependent transcription in lymphocytes
7 Signaling events mediated by HDAC Class I
8 Regulation of retinoblastoma protein
Reactome RORA activates gene expression Click to Show/Hide
2 BMAL1:CLOCK,NPAS2 activates circadian gene expression
3 Recycling of bile acids and salts
4 PPARA activates gene expression
5 Import of palmitoyl-CoA into the mitochondrial matrix
6 YAP1- and WWTR1 (TAZ)-stimulated gene expression
7 Regulation of pyruvate dehydrogenase (PDH) complex
8 Endogenous sterols
9 Transcriptional activation of mitochondrial biogenesis
10 Activation of gene expression by SREBF (SREBP)
11 Transcriptional regulation of white adipocyte differentiation
12 Nuclear Receptor transcription pathway
13 Regulation of lipid metabolism by Peroxisome proliferator-activated receptor alpha (PPARalpha)
14 Circadian Clock
WikiPathways Vitamin A and Carotenoid Metabolism Click to Show/Hide
2 NRF2 pathway
3 Nuclear Receptors Meta-Pathway
4 Farnesoid X Receptor Pathway
5 PPAR Alpha Pathway
6 Vitamin D Receptor Pathway
7 Pregnane X Receptor pathway
8 Constitutive Androstane Receptor Pathway
9 Liver X Receptor Pathway
10 Regulation of Lipid Metabolism by Peroxisome proliferator-activated receptor alpha (PPARalpha)
11 Transcriptional Regulation of White Adipocyte Differentiation
12 YAP1- and WWTR1 (TAZ)-stimulated gene expression
13 Activation of Gene Expression by SREBP (SREBF)
14 Integrated Pancreatic Cancer Pathway
15 Adipogenesis
16 Circadian Clock
17 Nuclear Receptors
18 Vitamin D Metabolism
19 Wnt Signaling Pathway Netpath
20 Nuclear Receptors in Lipid Metabolism and Toxicity
21 Differentiation of white and brown adipocyte
22 SREBP signalling
References
Reference 1 GW9662, a potent antagonist of PPARgamma, inhibits growth of breast tumour cells and promotes the anticancer effects of the PPARgamma agonist rosiglitazone, independently of PPARgamma activation. Br J Pharmacol. 2004 Dec;143(8):933-7.
Reference 2 Synergistic Antiproliferative Effects of Combined Gamma -Tocotrienol and PPAR Gamma Antagonist Treatment Are Mediated through PPAR Gamma -Independent Mechanisms in Breast Cancer Cells. PPAR Res. 2014;2014:439146.
Reference 3 The Protein Data Bank. Nucleic Acids Res. 2000 Jan 1;28(1):235-42.
 Download Picture         KEGG Link      
 Download Picture         KEGG Link      
 Download Picture         KEGG Link      
 Download Picture         KEGG Link      
 Download Picture         KEGG Link      
Cite NPCDR
Visitor Map
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