Isolation, Cytotoxicity Evaluation, Docking, ADMET and Drug Likeness Studies of Secondary Metabolites from the Stem Bark of Anthocephalus cadamba (Roxb.)

被引:12
|
作者
Gupta, Nidhi [1 ,2 ]
Qayum, Arem [3 ]
Singh, Shashank [3 ]
Mujwar, Somdutt [4 ]
Sangwan, Payare L. [1 ]
机构
[1] CSIR Indian Inst Integrat Med, Nat Prod & Med Chem NPMC Div, Jammu 180001, India
[2] Maharishi Markandeshwar Deemed Univ, MM Coll Pharm, Dept Pharmaceut Chem, Mullana Ambala 133207, Haryana, India
[3] CSIR Indian Inst Integrat Med, Canc Pharmacol Div, Jammu 180001, India
[4] Chitkara Univ, Chitkara Coll Pharm, Rajpura 140401, Punjab, India
来源
CHEMISTRYSELECT | 2022年 / 7卷 / 43期
关键词
A; cadamba; Secondary Metabolites; Anticancer; Docking; ADMET; Drug likeness; METHANOLIC EXTRACT; NEOLAMARCKIA-CADAMBA; ANTIOXIDANT; ACID; GLYCOSIDES; INHIBITOR; DISCOVERY;
D O I
10.1002/slct.202202950
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Phytochemical investigation of the stem bark of Anthocephalus cadamba(Rubiaceae) led to the isolation of total ten secondary metabolites (1-10) including beta-sitosterol (1), ursolic acid (2), vanillic acid (3), quinovic acid (4), 3-O-[alpha-L-rhamnopyranosyl]-quinovic acid (5), beta-sitosterol beta-D-glucoside (6), cadambine (7), 3 beta-dihydrocadambine (8), 7-O-acetyl loganin (9) and hexyl p-coumarate (10). Four acetylated derivatives 2 a,5 a,7 aand8 aobtained through acetylation of compounds 2, 5, 7 and 8 respectively. All the compounds characterized using H-1 and (CNMR)-C-13, HRESIMS and IR and comparison with literature. Compound 4showed the best cytotoxic activity with IC50 value 4 and 7 mu M against pancreatic (MIA-pa-Ca-2) and leukemia (HL-60) cancer cells respectively. Docking results supported the anticancer potential of compound 4via inhibition of EGFR receptor (PDB ID:3POZ) and its pharmacokinetic profile found optimized as per the Lipinski's filter. Therefore compound 4has the potential to be developed as an anticancer agent against pancreatic cancer cells.
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页数:12
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