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ChemicalBook--->CAS DataBase List--->15503-86-3

15503-86-3

15503-86-3 Structure

15503-86-3 Structure
IdentificationBack Directory
[Name]

isatidine
[CAS]

15503-86-3
[Synonyms]

isatidine
Retrorsin-N-oxid
RETRORSINE-N-OXIDE
12,18-Dihydroxy-11,16-dioxosenecionane 4-oxide
12,18-Dihydroxysenecionane-11,16-dione 4-oxide
[1,6]Dioxacyclododecino[2,3,4-gh]pyrrolizine-2,7-dione, 3-ethylidene-3,4,5,6,9,11,13,14,14a,14b-decahydro-6-hydroxy-6-(hydroxymethyl)-5-methyl-, 12-oxide, (3Z,5R,6S,14aR,14bR)-
[Molecular Formula]

C18H25NO7
[MDL Number]

MFCD00074872
[MOL File]

15503-86-3.mol
[Molecular Weight]

367.396
Chemical PropertiesBack Directory
[Melting point ]

145°C
[Boiling point ]

497.95°C (rough estimate)
[density ]

1.3204 (rough estimate)
[refractive index ]

1.5100 (estimate)
[pka]

11.96±0.40(Predicted)
[IARC]

3 (Vol. 10, Sup 7) 1987
[EPA Substance Registry System]

Isatidine (15503-86-3)
Safety DataBack Directory
[RIDADR ]

1544
[HazardClass ]

6.1(a)
[PackingGroup ]

II
[Safety Profile]

Poison by ingestion and intraperitoneal routes. Moderately toxic by intravenous route. Questionable carcinogen with experimental neoplastigenic and tumorigenic data. Mutation data reported. When heated to decomposition it emits toxic fumes of NO,. See also ESTERS.
[Hazardous Substances Data]

15503-86-3(Hazardous Substances Data)
Hazard InformationBack Directory
[Description]

This hepatotoxic alkaloid occurs in certain Senecio species and was first isolated from S. isatideus D.C. It occurs abundantly in S. retrorsus D.C. and S. scleratus Schw. The alkaloid crystallizes in rhombic prisms as the dihydrate and has [α]27D . 8.25° (H 20). It is soluble in MeOH, hot EtOH and hot H20 but virtually insoluble in Et 20, Me2CO or CHCl 3. On reduction it absorbs 4 molecules of H2 to give hexahydrodeoxyisatidine which melts at l15-l20°C and then remelts at l83-4°C following an intermediate solidification. This compound gives a hydrochloride, m.p. 218°C (dec.); [α]20D - 52.5° (H20) and may be hydrolyzed with Ba(OHh to give a basic product, tetrahydroisatinecine, CSH1703N, m.p. l74.5°C; [α]20D - 88° (H 20). The alkaloid itself, on hydrolysis with Ba(OHh yields isatinecine and two acid products, isatinecic acid and the monolactone, the latter almost certainly being formed by the action of the base upon the acid.
[Uses]

Retrorsine N-oxide-D4 is a labelled analogue of Retrorsine N-oxide (R279005). Retrorsine N-oxide is a pyrrolizidine alkaloid that is naturally found in Senecio isatideus, a flowering plant that is native to the Netherlands. Retrorsine N-oxide is also known to raise blood pressure and can induce abnormal changes in the liver if ingested by animals or humans.
[Definition]

ChEBI: Isatidine is a citraconoyl group.
[References]

Blackie., Pharrn. J., 138, 102 (1937) de Waal., Onderstepoort J., 12, 155 (1939) de Waal., Nature, 146, 777 (1940) de Waal., Pretorius., OnderstepoortJ., 17,181 (1941) Leisegang, Warren., J. Chern. Soc., 702 (1950)
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