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2348-82-5

2348-82-5 | 1,4-Naphthalenedione, 2-methoxy-

CAS No: 2348-82-5 Catalog No: AG002NDL MDL No:MFCD00019539

Product Description

Catalog Number:
AG002NDL
Chemical Name:
1,4-Naphthalenedione, 2-methoxy-
CAS Number:
2348-82-5
Molecular Formula:
C11H8O3
Molecular Weight:
188.1794
MDL Number:
MFCD00019539
IUPAC Name:
2-methoxynaphthalene-1,4-dione
InChI:
InChI=1S/C11H8O3/c1-14-10-6-9(12)7-4-2-3-5-8(7)11(10)13/h2-6H,1H3
InChI Key:
OBGBGHKYJAOXRR-UHFFFAOYSA-N
SMILES:
COC1=CC(=O)c2c(C1=O)cccc2
UNII:
39020BUT1D
NSC Number:
31530

Properties

Complexity:
304  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
188.047g/mol
Formal Charge:
0
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
188.182g/mol
Monoisotopic Mass:
188.047g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
43.4A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.4  

Literature

Title Journal
2-Methoxy-1,4-Naphthoquinone (MNQ) suppresses the invasion and migration of a human metastatic breast cancer cell line (MDA-MB-231). Toxicology in vitro : an international journal published in association with BIBRA 20140401
New oxirane derivatives of 1,4-naphthoquinones and their evaluation against T. cruzi epimastigote forms. Bioorganic & medicinal chemistry 20120815
2-Meth-oxy-naphthalene-1,4-dione. Acta crystallographica. Section E, Structure reports online 20110401
In Vitro Activity of 2-methoxy-1,4-naphthoquinone and Stigmasta-7,22-diene-3β-ol from Impatiens balsamina L. against Multiple Antibiotic-Resistant Helicobacter pylori. Evidence-based complementary and alternative medicine : eCAM 20110101
Antifungal activity of lawsone methyl ether in comparison with chlorhexidine. Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology 20110101
2-methoxy-1,4-naphthoquinone isolated from Impatiens balsamina in a screening program for activity to inhibit Wnt signaling. Journal of natural medicines 20110101
Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis. Bioorganic & medicinal chemistry letters 20101101
Substituted naphthoquinones as novel amino acid sensitive reagents for the detection of latent fingermarks on paper surfaces. Talanta 20101015
Naphthoquinones and anthraquinones from scent glands of a dyspnoid Harvestman, Paranemastoma quadripunctatum. Journal of chemical ecology 20100201
Indoleamine 2,3-dioxygenase is the anticancer target for a novel series of potent naphthoquinone-based inhibitors. Journal of medicinal chemistry 20080327
Isolation and identification of an anti-tumor component from leaves of Impatiens balsamina. Molecules (Basel, Switzerland) 20080131
Effects of the compounds 2-methoxynaphthoquinone, 2-propoxynaphthoquinone, and 2-isopropoxynaphthoquinone on ecdysone 20-monooxygenase activity. Archives of insect biochemistry and physiology 20070901
Structure-activity relationships in the haemolytic activity and nephrotoxicity of derivatives of 1,2- and 1,4-naphthoquinone. Journal of applied toxicology : JAT 20070101
Microsphere-based protease assays and screening application for lethal factor and factor Xa. Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501
Design, synthesis, and biological evaluation of prazosin-related derivatives as multipotent compounds. Journal of medicinal chemistry 20050113
Photoreactions of 1,4-Naphthoquinones: effects of substituents and water on the intermediates and reactivity. Photochemistry and photobiology 20050101
Role of oxidant stress in lawsone-induced hemolytic anemia. Toxicological sciences : an official journal of the Society of Toxicology 20041201
Discovery, total synthesis, HRV 3C-protease inhibitory activity, and structure-activity relationships of 2-methoxystypandrone and its analogues. Bioorganic & medicinal chemistry letters 20011217
Isolation of an antimicrobial compound from Impatiens balsamina L. using bioassay-guided fractionation. Phytotherapy research : PTR 20011201

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