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ChemicalBook--->CAS DataBase List--->84-26-4

84-26-4

84-26-4 Structure

84-26-4 Structure
IdentificationMore
[Name]

Rutaecarpine
[CAS]

84-26-4
[Synonyms]

8,13-DIHYDRO-INDOLO[2'3':3,4]PYRIDO[2,1-B]QUINAZOLIN-5(7H)-ONE
RHETINE
RUTAECARPINE
RUTECARPINE
RUTECARPINE 95+
Rutaecarpine std.
Rutaecarpine
Indolo[2',3':3,4]pyrido[2,1-b]quinazolin-5(7H)-one,8,13-dihydro-
Rutecarpine, 8,13-Dihydroindolo[2μ,3μ:3,4]pyrido[2,1-b]quinazolin-5(7H)-one
5,7,8,13-Tetrahydroindolo[2',3':3,4]pyrido[2,1-b]quinazoline-5-one
[EINECS(EC#)]

635-907-6
[Molecular Formula]

C18H13N3O
[MDL Number]

MFCD00210551
[Molecular Weight]

287.32
[MOL File]

84-26-4.mol
Chemical PropertiesBack Directory
[Melting point ]

259.5-260°
[Boiling point ]

429.62°C (rough estimate)
[density ]

1.2030 (rough estimate)
[refractive index ]

1.5855 (estimate)
[storage temp. ]

2-8°C
[solubility ]

DMSO: 18 mg/mL clear yellow solution, soluble
[form ]

solid
[pka]

15.79±0.20(Predicted)
[color ]

white
[Merck ]

14,8298
[InChIKey]

ACVGWSKVRYFWRP-UHFFFAOYSA-N
[CAS DataBase Reference]

84-26-4(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

T
[Risk Statements ]

R25:Toxic if swallowed.
[Safety Statements ]

S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
[RIDADR ]

UN 2811 6.1/PG 3
[WGK Germany ]

3
[RTECS ]

NM3454000
[HS Code ]

29339900
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

Rutaecarpine(84-26-4).msds
Hazard InformationBack Directory
[Description]

This alkaloid occurs with Evodiamine (q.v.) in the Chinese drug 'Wou-chou-yu' which is the dried fruit of Evodia rutaecarpa Benth. It crystallizes from boiling EtOH as colourless, or pale yellow, needles and is optically inactive. The acetyl derivative has m.p. 184-6°C and the benzoyl compound, m.p. 194°C. The alkaloid gives a yellow colour with concentrated H2S04 and is decomposed by KOH in boiling amyl alcohol yielding anthranilic acid and 3-{3-aminoethylindole- 2-O!carboxylic acid, CllH120 2N2, silky crystals, m.p. 257°C.
Pharmacologically, the alkaloid causes increased arterial pressure on injection.
[Chemical Properties]

Solid
[Uses]

Rutaecarpine is an indole alkaloid contained in the fruit of Evodiae fruits. It been shown to ameliorate bodyweight gain through orexigenic neuropeptides NPY and AgRP. It also playes a role in the treatment of high blood pressure
[Definition]

ChEBI:Rutecarpine is a member of beta-carbolines.
[in vivo]

Rutaecarpine showed in vivo anti-inflammatory activity on rat l-carrageenan induced paw edema by intraperitoneal administration[1]. Rutaecarpine significantly decreases the number of antibody-forming cells and causes weight decrease in spleen in a dose-dependent manner. In addition, rutaecarpine administered mice exhibit reduced splenic cellularity, decreased numbers of total T cells, CD4+ cells, CD8+ cells, and B cells in spleen. IL-2, interferon and IL-10 mRNA expressions are suppressed significantly by rutaecarpine treatment. The number of CD4+IL-2+ cells is reduced significantly following administration of mice with rutaecarpine[3].

[IC 50]

COX-2: 0.28 μM (IC50, in BMMC); COX-1: 8.7 μM (IC50, in BMMC)
[References]

Asahina, Kashiwagi., J. Pharm. Chim., 14,54 (1916)
Asahina, Mayeda.,J. Pharm. Soc., Japan, No. 416 (1916)
Asahina, Fujita., ibid, 863 (1921)
Kermack, Perkin, Robinson.,J. Chem. Soc., 119,1615 (1921)
Asahina, Manske, Robinson., ibid, 1708 (1927)
Asahina, Irie, Ohta., J. Pharm. Soc., Japan, 48, 51 (1928)
Ohta., ibid, 60, 109 (1940)
Schopf, Steuer., Annalen, 558, 124 (1947)
Biosynthesis:
Yamazaki, Ikuta., Tetrahedron Lett., 3221 (1966)
Yamazakietal., ibid, 3317 (1967)
Pharmacology:
Raymond-Hamet., Cornpt. rend., 220, 749 (1945)
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

84-26-4(sigmaaldrich)
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