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⚫ {{distinguish|rhodamine}}

{{chembox {{chembox
| Watchedfields = changed
| verifiedrevid = 417956840 | verifiedrevid = 464381819
|Reference=<ref> at ]</ref> | Reference = <ref> at ]</ref>
|ImageFile=Rhodanine transparant.png
| ImageFile = Rhodanine.svg
|ImageSize=150px | ImageSize = 150px
|IUPACName=2-Sulfanylidene-1,3-thiazolidin-4-one | PIN = 2-Sulfanylidene-1,3-thiazolidin-4-one
|OtherNames=2-Thioxo-4-thiazolidinone; 4-Oxo-2-thioxothiazoline | OtherNames = 2-Thioxo-4-thiazolidinone; 4-Oxo-2-thioxothiazoline
⚫ |Section1={{Chembox Identifiers

⚫ | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
⚫ |Section1 = {{Chembox Identifiers
⚫ | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 1013337 | ChemSpiderID = 1013337
| InChI = 1/C3H3NOS2/c5-2-1-7-3(6)4-2/h1H2,(H,4,5,6) | InChI = 1/C3H3NOS2/c5-2-1-7-3(6)4-2/h1H2,(H,4,5,6)
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| ChEMBL_Ref = {{ebicite|correct|EBI}} | ChEMBL_Ref = {{ebicite|correct|EBI}}
| ChEMBL = 224633 | ChEMBL = 224633
| EC_number = 205-505-1
| KEGG = C07280
| StdInChI_Ref = {{stdinchicite|correct|chemspider}} | StdInChI_Ref = {{stdinchicite|correct|chemspider}}
| StdInChI = 1S/C3H3NOS2/c5-2-1-7-3(6)4-2/h1H2,(H,4,5,6) | StdInChI = 1S/C3H3NOS2/c5-2-1-7-3(6)4-2/h1H2,(H,4,5,6)
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} | StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey = KIWUVOGUEXMXSV-UHFFFAOYSA-N | StdInChIKey = KIWUVOGUEXMXSV-UHFFFAOYSA-N
| CASNo_Ref = {{cascite|correct|CAS}}
| CASNo=141-84-4 | CASNo =141-84-4
⚫ | PubChem=1201546
| UNII_Ref = {{fdacite|correct|FDA}}
⚫ | SMILES = O=C1NC(=S)SC1
| UNII = 7O50LKL2G8
⚫ | PubChem =1201546
⚫ | SMILES = O=C1NC(=S)SC1
}} }}

|Section2={{Chembox Properties | Section2 = {{Chembox Properties
| C=3|H=3|N=1|O=1|S=2 | C=3 | H=3 | N=1 | O=1 | S=2
| Appearance=
| Appearance =
| Density=
| Density = 0.868 g/cm<sup>−3</sup><ref name=b1/>
| MeltingPt=165-169 °C
| MeltingPtC = 170
| BoilingPt=
| MeltingPt_ref = <ref name=b1>{{cite book | editor= Haynes, William M. | year = 2011 | title = CRC Handbook of Chemistry and Physics | edition = 92nd | publisher = ] | isbn = 978-1439855119|page=3.512| title-link = CRC Handbook of Chemistry and Physics }}</ref>
| Solubility=
| BoilingPt =
| Solubility = Soluble<ref name=b1/>
| SolubleOther = Ethanol, dimethyl sulfoxide<ref name=b1/>
}} }}

|Section3={{Chembox Hazards | Section3 = {{Chembox Hazards
| MainHazards=
| MainHazards =
| FlashPt=
| FlashPt =
| Autoignition=
| AutoignitionPt =
| EUClass = {{Hazchem Xn}}
| RPhrases = {{R22}} {{R41}} | GHSPictograms = {{GHS05}}{{GHS07}}
| GHSSignalWord = Danger
| SPhrases = {{S22}} {{S26}} {{S39}}
| HPhrases = {{H-phrases|302|318}}
| PPhrases = {{P-phrases|264|270|280|301+312|305+351+338|310|330|501}}
}} }}
}} }}
⚫ {{distinguish|rhodamine}}
⚫ '''Rhodanine''' is an ] derived from ]. Rhodanine can be prepared by the reaction of ], ], and ].<ref>{{cite journal | title = Rhodanine | author = Redemann; Icke; Alles | journal = Organic Syntheses | year = 1947 | volume = 27 | page = 74}}</ref>


'''Rhodanine''' is a 5-membered ] ] possessing a ] core. It was discovered in 1877 by ] who named it ''"Rhodaninsaure"'' in reference to its synthesis from ammonium rhodanide (known as ] to modern chemists) and ] in water.<ref>{{cite journal|last1=Nencki|first1=M.|title=Ueber die Einwirkung der Monochloressigsäure auf Sulfocyansäure und ihre Salze|journal=Journal für Praktische Chemie|date=10 July 1877|volume=16|issue=1|pages=1–17|doi=10.1002/prac.18770160101|url=https://zenodo.org/record/1427872}}</ref>
Some derivatives of rhodanine have pharmacological properties, such as ] which is used to treat ].

⚫ Rhodanines can also be prepared by the reaction of ], ], and ], which proceeds via an intermediate ].<ref>{{OrgSynth | title = Rhodanine | author1 = Redemann, C. Ernst | author2 = Icke, Roland N. | author3 = Alles, Gordon A. | year = 1955 | collvol = 3 | collvolpages = 763 | prep = cv3p0763 }}</ref>

:]

==Derivatives==
Some rhodanine ] have pharmacological properties; for instance, ] is used to treat ]. However, most are promiscuous binders with poor selectivity; as a result, this class of compounds is viewed with suspicion by medicinal chemists.<ref>{{cite journal | journal = J. Med. Chem. | year = 2010 | volume = 53 | pages = 2719–2740 | doi = 10.1021/jm901137j | pmid = 20131845 | title = New substructure filters for removal of pan assay interference compounds (PAINS) from screening libraries and for their exclusion in bioassays | issue = 7| last1 = Baell | first1 = J. B | last2 = Holloway | first2 = G. A | citeseerx = 10.1.1.394.9155 }}</ref><ref>{{cite journal | doi = 10.1517/17460441.2012.688743 | pmid = 22607309 | title = Rhodanine as a scaffold in drug discovery: A critical review of its biological activities and mechanisms of target modulation | year = 2012 | last1 = Tomašić | first1 = Tihomir | last2 = Peterlin Mašič | first2 = Lucija | journal = Expert Opinion on Drug Discovery | pages = 549–60 | volume=7| issue = 7 | s2cid = 3401210 }}</ref><ref>{{cite journal|last1=Pouliot|first1=Martin|last2=Jeanmart|first2=Stephane|title=Pan Assay Interference Compounds (PAINS) and Other Promiscuous Compounds in Antifungal Research|journal=Journal of Medicinal Chemistry|date=8 September 2015|pages=497–503|doi=10.1021/acs.jmedchem.5b00361|volume=59|issue=2|pmid=26313340}}</ref> Differing academic opinions exist concerning the correct use of ] filters, the necessity of the experimental confirmations of such properties, and many useful features of rhodanine derivatives.<ref>{{cite journal | journal = Expert Opinion on Drug Discovery | year = 2017 | volume = 12 | pages = 1233–1252 | doi = 10.1080/17460441.2017.1388370 | pmid = 29019278 | title = Recent developments with rhodanine as a scaffold for drug discovery | issue = 12| last1 = Kaminskyy | first1 = D | last2 = Kryshchyshyn | first2 = A | last3 = Lesyk | first3 = R | s2cid = 3514481 }}</ref><ref>{{cite journal | journal = Eur. J. Med. Chem. | year = 2017 | volume = 140 | pages = 542–594 | doi = 10.1016/j.ejmech.2017.09.031 | pmid = 28987611 | title = 5-Ene-4-thiazolidinonese An efficient tool in medicinal chemistry | issue = 10| last1 = Kaminskyy | first1 = D | last2 = Kryshchyshyn | first2 = A | last3 = Lesyk | first3 = R | pmc = 7111298 }}</ref>


==References== ==References==
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] ]
] ]
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Latest revision as of 02:01, 25 December 2023

Not to be confused with rhodamine.
Rhodanine
Names
Preferred IUPAC name 2-Sulfanylidene-1,3-thiazolidin-4-one
Other names 2-Thioxo-4-thiazolidinone; 4-Oxo-2-thioxothiazoline
Identifiers
CAS Number
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.005.005 Edit this at Wikidata
EC Number
  • 205-505-1
KEGG
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C3H3NOS2/c5-2-1-7-3(6)4-2/h1H2,(H,4,5,6)Key: KIWUVOGUEXMXSV-UHFFFAOYSA-N
  • InChI=1/C3H3NOS2/c5-2-1-7-3(6)4-2/h1H2,(H,4,5,6)Key: KIWUVOGUEXMXSV-UHFFFAOYAP
SMILES
  • O=C1NC(=S)SC1
Properties
Chemical formula C3H3NOS2
Molar mass 133.18 g·mol
Density 0.868 g/cm
Melting point 170 °C (338 °F; 443 K)
Solubility in water Soluble
Solubility Ethanol, dimethyl sulfoxide
Hazards
GHS labelling:
Pictograms GHS05: CorrosiveGHS07: Exclamation mark
Signal word Danger
Hazard statements H302, H318
Precautionary statements P264, P270, P280, P301+P312, P305+P351+P338, P310, P330, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). checkY verify (what is  ?) Infobox references
Chemical compound

Rhodanine is a 5-membered heterocyclic organic compound possessing a thiazolidine core. It was discovered in 1877 by Marceli Nencki who named it "Rhodaninsaure" in reference to its synthesis from ammonium rhodanide (known as ammonium thiocyanate to modern chemists) and chloroacetic acid in water.

Rhodanines can also be prepared by the reaction of carbon disulfide, ammonia, and chloroacetic acid, which proceeds via an intermediate dithiocarbamate.

Derivatives

Some rhodanine derivatives have pharmacological properties; for instance, epalrestat is used to treat diabetic neuropathy. However, most are promiscuous binders with poor selectivity; as a result, this class of compounds is viewed with suspicion by medicinal chemists. Differing academic opinions exist concerning the correct use of PAINS filters, the necessity of the experimental confirmations of such properties, and many useful features of rhodanine derivatives.

References

  1. Rhodanine at Sigma-Aldrich
  2. ^ Haynes, William M., ed. (2011). CRC Handbook of Chemistry and Physics (92nd ed.). CRC Press. p. 3.512. ISBN 978-1439855119.
  3. Nencki, M. (10 July 1877). "Ueber die Einwirkung der Monochloressigsäure auf Sulfocyansäure und ihre Salze". Journal für Praktische Chemie. 16 (1): 1–17. doi:10.1002/prac.18770160101.
  4. Redemann, C. Ernst; Icke, Roland N.; Alles, Gordon A. (1955). "Rhodanine". Organic Syntheses; Collected Volumes, vol. 3, p. 763.
  5. Baell, J. B; Holloway, G. A (2010). "New substructure filters for removal of pan assay interference compounds (PAINS) from screening libraries and for their exclusion in bioassays". J. Med. Chem. 53 (7): 2719–2740. CiteSeerX 10.1.1.394.9155. doi:10.1021/jm901137j. PMID 20131845.
  6. Tomašić, Tihomir; Peterlin Mašič, Lucija (2012). "Rhodanine as a scaffold in drug discovery: A critical review of its biological activities and mechanisms of target modulation". Expert Opinion on Drug Discovery. 7 (7): 549–60. doi:10.1517/17460441.2012.688743. PMID 22607309. S2CID 3401210.
  7. Pouliot, Martin; Jeanmart, Stephane (8 September 2015). "Pan Assay Interference Compounds (PAINS) and Other Promiscuous Compounds in Antifungal Research". Journal of Medicinal Chemistry. 59 (2): 497–503. doi:10.1021/acs.jmedchem.5b00361. PMID 26313340.
  8. Kaminskyy, D; Kryshchyshyn, A; Lesyk, R (2017). "Recent developments with rhodanine as a scaffold for drug discovery". Expert Opinion on Drug Discovery. 12 (12): 1233–1252. doi:10.1080/17460441.2017.1388370. PMID 29019278. S2CID 3514481.
  9. Kaminskyy, D; Kryshchyshyn, A; Lesyk, R (2017). "5-Ene-4-thiazolidinonese An efficient tool in medicinal chemistry". Eur. J. Med. Chem. 140 (10): 542–594. doi:10.1016/j.ejmech.2017.09.031. PMC 7111298. PMID 28987611.
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