Amocarzine
PubChem CID
5464102
Structure
Molecular Formula
Synonyms
- Amocarzine
- Phenthiourezine
- 36590-19-9
- Amocarzina
- Amocarzinum
Molecular Weight
371.5 g/mol
Computed by PubChem 2.2 (PubChem release 2024.11.20)
Dates
- Create:2005-08-08
- Modify:2025-01-04
Description
Amocarzine is a thiourea resulting from the formal condensation of the secondary amino group of 1-methylpiperazine and the primary amino group of N-(4-nitrophenyl)benzene-1,4-diamine with carbonothioic O,O-acid. It has a role as an antinematodal drug. It is a C-nitro compound, a N-methylpiperazine, a member of thioureas and a secondary amino compound. It is functionally related to a diphenylamine.
Chemical Structure Depiction
4-methyl-N-[4-(4-nitroanilino)phenyl]piperazine-1-carbothioamide
Computed by Lexichem TK 2.7.0 (PubChem release 2024.11.20)
InChI=1S/C18H21N5O2S/c1-21-10-12-22(13-11-21)18(26)20-16-4-2-14(3-5-16)19-15-6-8-17(9-7-15)23(24)25/h2-9,19H,10-13H2,1H3,(H,20,26)
Computed by InChI 1.07.0 (PubChem release 2024.11.20)
UFLRJROFPAGRPN-UHFFFAOYSA-N
Computed by InChI 1.07.0 (PubChem release 2024.11.20)
CN1CCN(CC1)C(=S)NC2=CC=C(C=C2)NC3=CC=C(C=C3)[N+](=O)[O-]
Computed by OEChem 2.3.0 (PubChem release 2024.12.12)
C18H21N5O2S
Computed by PubChem 2.2 (PubChem release 2024.11.20)
99402-78-5
- 4-nitro-4'-(N-methyl)piperazinyl thiocarbonylidodiphenylamine
- amocarzine
- CGP 6140
- CGP-6140
- phenithiourezine
- Amocarzine
- Phenthiourezine
- 36590-19-9
- Amocarzina
- Amocarzinum
- Amocarzine [INN]
- Amocarzinum [INN-Latin]
- Amocarzina [INN-Spanish]
- CGP 6140
- CHEBI:38946
- UNII-99807U412Y
- AMOCARZINE [MI]
- AMOCARZINE [MART.]
- AMOCARZINE [WHO-DD]
- 99807U412Y
- 4-Nitro-4'-(N-methyl)piperazinyl thiocarbonylidodiphenylamine
- 4-methyl-N-[4-(4-nitroanilino)phenyl]piperazine-1-carbothioamide
- S 80016
- 4-Methyl-4'-(p-nitroanilino)thio-1-piperazinecarboxanilide
- CGP 6140; Phenthiourezine; S 80016
- Amocarzinum (INN-Latin)
- 4-methyl-N-(4-((4-nitrophenyl)amino)phenyl)-1-piperazinecarbothioamide
- 4-methyl-N-(4-((4-nitrophenyl)amino)phenyl)piperazine-1-carbothioamide
- 4-Methyl-N-[4-[(4-nitrophenyl)amino]phenyl]-1-piperazinecarbothioamide
- 4-methyl-N-{4-[(4-nitrophenyl)amino]phenyl}piperazine-1-carbothioamide
- Amocarzina (INN-Spanish)
- AMOCARZINE (MART.)
- Cgp-6140
- phenithiourezine
- 1-Piperazinecarbothioamide, 4-methyl-N-(4-((4-nitrophenyl)amino)phenyl)-
- cgp6140
- 1-PIPERAZINECARBOTHIOAMIDE,4-METHYL-N-[4-[(4-NITROPHENYL)AMINO]PHENYL]-
- S-80016
- SCHEMBL157806
- CHEMBL469328
- DTXSID90865827
- BCP28101
- DB-263203
- NS00125635
- Q27118042
- 4-Methyl-N-[4-[(4-nitrophenyl)amino]phenyl ]-1-piperazinecarbothioamide
Property Name
Property Value
Reference
Property Name
Molecular Weight
Property Value
371.5 g/mol
Reference
Computed by PubChem 2.2 (PubChem release 2024.11.20)
Property Name
XLogP3-AA
Property Value
2.9
Reference
Computed by XLogP3 3.0 (PubChem release 2024.11.20)
Property Name
Hydrogen Bond Donor Count
Property Value
2
Reference
Computed by Cactvs 3.4.8.18 (PubChem release 2024.11.20)
Property Name
Hydrogen Bond Acceptor Count
Property Value
5
Reference
Computed by Cactvs 3.4.8.18 (PubChem release 2024.11.20)
Property Name
Rotatable Bond Count
Property Value
3
Reference
Computed by Cactvs 3.4.8.18 (PubChem release 2024.11.20)
Property Name
Exact Mass
Property Value
371.14159610 Da
Reference
Computed by PubChem 2.2 (PubChem release 2024.11.20)
Property Name
Monoisotopic Mass
Property Value
371.14159610 Da
Reference
Computed by PubChem 2.2 (PubChem release 2024.11.20)
Property Name
Topological Polar Surface Area
Property Value
108 Ų
Reference
Computed by Cactvs 3.4.8.18 (PubChem release 2024.11.20)
Property Name
Heavy Atom Count
Property Value
26
Reference
Computed by PubChem
Property Name
Formal Charge
Property Value
0
Reference
Computed by PubChem
Property Name
Complexity
Property Value
476
Reference
Computed by Cactvs 3.4.8.18 (PubChem release 2024.11.20)
Property Name
Isotope Atom Count
Property Value
0
Reference
Computed by PubChem
Property Name
Defined Atom Stereocenter Count
Property Value
0
Reference
Computed by PubChem
Property Name
Undefined Atom Stereocenter Count
Property Value
0
Reference
Computed by PubChem
Property Name
Defined Bond Stereocenter Count
Property Value
0
Reference
Computed by PubChem
Property Name
Undefined Bond Stereocenter Count
Property Value
0
Reference
Computed by PubChem
Property Name
Covalently-Bonded Unit Count
Property Value
1
Reference
Computed by PubChem
Property Name
Compound Is Canonicalized
Property Value
Yes
Reference
Computed by PubChem (release 2021.10.14)
Follow these links to do a live 2D search or do a live 3D search for this compound, sorted by annotation score. This section is deprecated (see here for details), but these live search links provide equivalent functionality to the table that was previously shown here.
Same Parent, Exact Count
Mixtures, Components, and Neutralized Forms Count
Similar Compounds (2D)
Similar Conformers (3D)
Anthelmintics
Agents that kill parasitic worms. They are used therapeutically in the treatment of HELMINTHIASIS in man and animal. (See all compounds classified as Anthelmintics.)
Filaricides
Pharmacological agents destructive to nematodes in the superfamily Filarioidea. (See all compounds classified as Filaricides.)
Patents are available for this chemical structure:
https://patentscope.wipo.int/search/en/result.jsf?inchikey=UFLRJROFPAGRPN-UHFFFAOYSA-N
- CAS Common ChemistryLICENSEThe data from CAS Common Chemistry is provided under a CC-BY-NC 4.0 license, unless otherwise stated.https://creativecommons.org/licenses/by-nc/4.0/
- ChemIDplusChemIDplus Chemical Information Classificationhttps://pubchem.ncbi.nlm.nih.gov/source/ChemIDplus
- EPA DSSTox4-Methyl-N-[4-(4-nitroanilino)phenyl]piperazine-1-carbothioamidehttps://comptox.epa.gov/dashboard/DTXSID90865827CompTox Chemicals Dashboard Chemical Listshttps://comptox.epa.gov/dashboard/chemical-lists/
- FDA Global Substance Registration System (GSRS)LICENSEUnless otherwise noted, the contents of the FDA website (www.fda.gov), both text and graphics, are not copyrighted. They are in the public domain and may be republished, reprinted and otherwise used freely by anyone without the need to obtain permission from FDA. Credit to the U.S. Food and Drug Administration as the source is appreciated but not required.https://www.fda.gov/about-fda/about-website/website-policies#linking
- ChEBI
- ChEMBLLICENSEAccess to the web interface of ChEMBL is made under the EBI's Terms of Use (http://www.ebi.ac.uk/Information/termsofuse.html). The ChEMBL data is made available on a Creative Commons Attribution-Share Alike 3.0 Unported License (http://creativecommons.org/licenses/by-sa/3.0/).http://www.ebi.ac.uk/Information/termsofuse.html
- Drug Gene Interaction database (DGIdb)LICENSEThe data used in DGIdb is all open access and where possible made available as raw data dumps in the downloads section.http://www.dgidb.org/downloadsAMOCARZINEhttps://www.dgidb.org/drugs/ncit:C72145
- Therapeutic Target Database (TTD)
- Human Metabolome Database (HMDB)LICENSEHMDB is offered to the public as a freely available resource. Use and re-distribution of the data, in whole or in part, for commercial purposes requires explicit permission of the authors and explicit acknowledgment of the source material (HMDB) and the original publication (see the HMDB citing page). We ask that users who download significant portions of the database cite the HMDB paper in any resulting publications.http://www.hmdb.ca/citing
- Metabolomics Workbench
- NCI Thesaurus (NCIt)LICENSEUnless otherwise indicated, all text within NCI products is free of copyright and may be reused without our permission. Credit the National Cancer Institute as the source.https://www.cancer.gov/policies/copyright-reuseNCI Thesaurushttps://ncit.nci.nih.gov
- Springer Nature
- Wikidataamocarzinehttps://www.wikidata.org/wiki/Q27118042
- PubChem
- Medical Subject Headings (MeSH)LICENSEWorks produced by the U.S. government are not subject to copyright protection in the United States. Any such works found on National Library of Medicine (NLM) Web sites may be freely used or reproduced without permission in the U.S.https://www.nlm.nih.gov/copyright.htmlAnthelminticshttps://www.ncbi.nlm.nih.gov/mesh/68000871Filaricideshttps://www.ncbi.nlm.nih.gov/mesh/68005369
- NORMAN Suspect List ExchangeLICENSEData: CC-BY 4.0; Code (hosted by ECI, LCSB): Artistic-2.0https://creativecommons.org/licenses/by/4.0/NORMAN Suspect List Exchange Classificationhttps://www.norman-network.com/nds/SLE/
- MolGenieMolGenie Organic Chemistry Ontologyhttps://github.com/MolGenie/ontology/
- PATENTSCOPE (WIPO)SID 397308855https://pubchem.ncbi.nlm.nih.gov/substance/397308855
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