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75013-64-8 | 2-acetylpyridine-4-methyl-3-thiosemicarbazone
CAS No: 75013-64-8 Catalog No: AG00GB0G MDL No:
Product Description
Catalog Number:
AG00GB0G
Chemical Name:
2-acetylpyridine-4-methyl-3-thiosemicarbazone
CAS Number:
75013-64-8
IUPAC Name:
1-methyl-3-[(E)-1-pyridin-2-ylethylideneamino]thiourea
InChI:
InChI=1S/C9H12N4S/c1-7(12-13-9(14)10-2)8-5-3-4-6-11-8/h3-6H,1-2H3,(H2,10,13,14)/b12-7+
InChI Key:
KDNWDIABXHFHBK-KPKJPENVSA-N
NSC Number:
293870
Properties
Complexity:
227
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1
Exact Mass:
208.078g/mol
Formal Charge:
0
Heavy Atom Count:
14
Hydrogen Bond Acceptor Count:
3
Hydrogen Bond Donor Count:
2
Isotope Atom Count:
0
Molecular Weight:
208.283g/mol
Monoisotopic Mass:
208.078g/mol
Rotatable Bond Count:
2
Topological Polar Surface Area:
81.4A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.1
Literature
| Title | Journal |
|---|---|
| Role of metalation in the topoisomerase IIα inhibition and antiproliferation activity of a series of α-heterocyclic-N4-substituted thiosemicarbazones and their Cu(II) complexes. | Journal of medicinal chemistry 20110414 |
| Mn(II), Co(II) and Zn(II) complexes with heterocyclic substituted thiosemicarbazones: synthesis, characterization, X-ray crystal structures and antitumor comparison. | European journal of medicinal chemistry 20100701 |
| Thiosemicarbazones, semicarbazones, dithiocarbazates and hydrazide/hydrazones: anti-Mycobacterium tuberculosis activity and cytotoxicity. | European journal of medicinal chemistry 20100501 |
| 2-Acetylpyridine thiosemicarbazones are potent iron chelators and antiproliferative agents: redox activity, iron complexation and characterization of their antitumor activity. | Journal of medicinal chemistry 20090312 |
| Thiosemicarbazones of 2-acetylpyridine, 2-acetylquinoline, 1-acetylisoquinoline, and related compounds as inhibitors of herpes simplex virus in vitro and in a cutaneous herpes guinea pig model. | Antiviral research 19860701 |
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