CAS 128-76-7|4H-Dibenzo[de,g]quinolin-9-ol,5,6,6a,7-tetrahydro-1,2,10-trimethoxy-, (6aS)-

Introduction:Basic information about CAS 128-76-7|4H-Dibenzo[de,g]quinolin-9-ol,5,6,6a,7-tetrahydro-1,2,10-trimethoxy-, (6aS)-, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common Name4H-Dibenzo[de,g]quinolin-9-ol,5,6,6a,7-tetrahydro-1,2,10-trimethoxy-, (6aS)-
CAS Number128-76-7Molecular Weight327.37400
Density1.239g/cm3Boiling Point524.4ºC at 760mmHg
Molecular FormulaC19H21NO4Melting Point/
MSDS/Flash Point270.9ºC

Names

Name1,2,10-trimethoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-9-ol

BiologicalActivity

DescriptionLaurotetanine ((+)-Laurotetanine) is an potent and orally active isoquinoline alkaloid and could be extracted from the roots of Litsea cubeba (Lour.) Pers. Laurotetanine exerts an anti-asthmatic effect by inhibition of IgE, histamine, and inflammatory reactions via down-regulating MUC5AC and NF-κB signaling pathways[1].
Related CatalogResearch Areas >>Cancer
In VivoLaurotetanine ((+)-Laurotetanine; 20-60 mg/kg; p.o.; 每天,持续 21 天; SD 大鼠) 通过下调 MUC5AC 和 NF-κB 信号通路发挥抗哮喘作用。 Animal Model: Sprague Dawley (SD) rats (180-220g) [1] Dosage: 20, 40, and 60 mg/kg Administration: Oral administration; daily, for 21 days Result: Reduced inflammatory cells, including eosinophils, neutrophils, lymphocytes, and macrophages. Decreased inflammatory cytokines viz IL-4, IL-6, IL-13 and increased IFN-γ. Reduced serum IgE and histamine. Decreased MUC5AC expression and increased NF-κB and IκB expression in lung tissues.
References

[1]. Xin XX, et, al. Anti-asthmatic effect of laurotetanine extracted from Litsea cubeba (Lour.) Pers. root on ovalbumin-induced allergic asthma rats, and elucidation of its mechanism of action. TROP J PHARM RES. 2019:18(6).

Chemical & Physical Properties

Density1.239g/cm3
Boiling Point524.4ºC at 760mmHg
Molecular FormulaC19H21NO4
Molecular Weight327.37400
Flash Point270.9ºC
Exact Mass327.14700
PSA59.95000
LogP3.15670
Vapour Pressure1.3E-11mmHg at 25°C
Index of Refraction1.605
InChIKeyGVVXPMORGFYVOO-ZDUSSCGKSA-N
SMILESCOc1cc2c(cc1O)CC1NCCc3cc(OC)c(OC)c-2c31

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
RB6025000
CHEMICAL NAME :
6a-alpha-Noraporphin-9-ol, 1,2,10-trimethoxy-
CAS REGISTRY NUMBER :
128-76-7
LAST UPDATED :
198208
DATA ITEMS CITED :
3
MOLECULAR FORMULA :
C19-H21-N-O4
MOLECULAR WEIGHT :
327.41
WISWESSER LINE NOTATION :
T C6666 1A Q KM&TT&J EO1 FQ PO1 QO1

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
450 mg/kg
TOXIC EFFECTS :
Cardiac - change in rate Vascular - BP lowering not characterized in autonomic section Lungs, Thorax, or Respiration - other changes
REFERENCE :
APFRAD Annales Pharmaceutiques Francaises. (SPPIF, B.P.22, F-41353 Vineuil, France) V.1- 1943- Volume(issue)/page/year: 38,537,1980
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
170 mg/kg
TOXIC EFFECTS :
Cardiac - change in rate Vascular - BP lowering not characterized in autonomic section Lungs, Thorax, or Respiration - other changes
REFERENCE :
APFRAD Annales Pharmaceutiques Francaises. (SPPIF, B.P.22, F-41353 Vineuil, France) V.1- 1943- Volume(issue)/page/year: 38,537,1980
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
90 mg/kg
TOXIC EFFECTS :
Cardiac - change in rate Vascular - BP lowering not characterized in autonomic section Lungs, Thorax, or Respiration - other changes
REFERENCE :
APFRAD Annales Pharmaceutiques Francaises. (SPPIF, B.P.22, F-41353 Vineuil, France) V.1- 1943- Volume(issue)/page/year: 38,537,1980
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