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Drug Details

General Information of the Drug (ID: DR7720)
Name
HLM006474
Synonyms
HLM006474; 353519-63-8; 7-[(4-ethoxy-3-methylphenyl)(2-pyridinylamino)methyl]-2-methyl-8-quinolinol; 7-[(4-ethoxy-3-methylphenyl)-(pyridin-2-ylamino)methyl]-2-methylquinolin-8-ol; 7-[(4-ethoxy-3-methylphenyl)(pyridin-2-ylamino)methyl]-2-methylquinolin-8-ol; Oprea1_498948; SCHEMBL9963974; CHEMBL4571419; BCP34559; EX-A3531; 3384AH; CCG-21518; s8963; STK509159; AKOS000357958; AKOS022004575; CS-3180; HLM 006474; MCULE-1162226397; NCGC00387261-01; HY-16667; EU-0079871; HLM006474, >=98% (HPLC); HLM-006474; HLM 006474; SR-01000502837; SR-01000502837-1
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Molecular Type
Small molecule
Disease Melanoma [ICD-11: 2C30] 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
C25H25N3O2
PubChem CID
2895500
Canonical SMILES
CCOC1=C(C=C(C=C1)C(C2=C(C3=C(C=CC(=N3)C)C=C2)O)NC4=CC=CC=N4)C
InChI
1S/C25H25N3O2/c1-4-30-21-13-11-19(15-16(21)2)23(28-22-7-5-6-14-26-22)20-12-10-18-9-8-17(3)27-24(18)25(20)29/h5-15,23,29H,4H2,1-3H3,(H,26,28)
InChIKey
CYNZBLNMIJNBSF-UHFFFAOYSA-N
Combinatorial Therapeutic Effect(s) Validated Clinically or Experimentally
    α. A List of Natural Product(s) Able to Enhance the Efficacy of This Drug
          Paclitaxel      Taxus brevifolia     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 E2F3  Molecule Info 
Pathway MAP
                    In-vitro Model NCI-H1299 CVCL_0060 Lung large cell carcinoma Homo sapiens
NCI-H292 CVCL_0455 Lung mucoepidermoid carcinoma Homo sapiens
                    Experimental
                    Result(s)
E2F inhibition synergizes with paclitaxel in lung cancer cell lines.
Target and Pathway
Target(s) Carbonic anhydrase IX (CA-IX)  Molecule Info  [3]
KEGG Pathway Nitrogen metabolism Click to Show/Hide
Pathway Interaction Database HIF-1-alpha transcription factor network Click to Show/Hide
Reactome Regulation of gene expression by Hypoxia-inducible Factor Click to Show/Hide
2 Reversible hydration of carbon dioxide
WikiPathways Vitamin D Receptor Pathway Click to Show/Hide
2 Reversible Hydration of Carbon Dioxide
3 Regulation of Hypoxia-inducible Factor (HIF) by Oxygen
References
Reference 1 A small-molecule E2F inhibitor blocks growth in a melanoma culture model. Cancer Res. 2008 Aug 1;68(15):6292-9.
Reference 2 E2F inhibition synergizes with paclitaxel in lung cancer cell lines. PLoS One. 2014 May 15;9(5):e96357.
Reference 3 Combined 3-O-acetylbetulin treatment and carbonic anhydrase IX inhibition results in additive effects on human breast cancer cells. Chem Biol Interact. 2021 Jan 5;333:109326.
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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