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About This Item
Empirical Formula (Hill Notation):
C16H18N2O
CAS Number:
Molecular Weight:
254.33
UNSPSC Code:
12352200
EC Number:
210-024-5
MDL number:
SMILES string
CN1C[C@H](CO)C=C2[C@H]1Cc3c[nH]c4cccc2c34
assay
97%
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 2 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Storage Class
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
Regulatory Information
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Anupam Maurya et al.
Biomedical chromatography : BMC, 26(9), 1096-1100 (2011-11-29)
A rapid, simple, sensitive, gradient and reproducible, reverse-phase high-performance liquid chromatographic method was developed for the quantitative estimation of bioactive alkaloids, lysergol and chanoclavine in the seeds of Ipomoea muricata. The clavine alkaloid, lysergol, is a bioenhancer for the drugs
S L Lodge-Ivey et al.
Journal of veterinary diagnostic investigation : official publication of the American Association of Veterinary Laboratory Diagnosticians, Inc, 18(4), 369-374 (2006-08-23)
Ergot alkaloids present in endophyte-infected tall fescue induce fescue toxicosis in livestock consuming the plant. The lysergic acid (LA) ring structure is a common moiety among the ergot alkaloids. Little is known about the bioavailability of LA because of limitations
V Kren et al.
Bioorganic & medicinal chemistry, 4(6), 869-876 (1996-06-01)
New glycosides derived from ergot alkaloids elymoclavine and DH-lysergol were synthesized by chemoenzymatic methods. beta-Glucosides were obtained either by chemical method or by transglycosylation (glycosidase from Aspergillus oryzae), lactosides were prepared by further extension of carbohydrate chain using beta-1,4-galactosyltransferase (bovine
D S Sveshnikov et al.
Aviakosmicheskaia i ekologicheskaia meditsina = Aerospace and environmental medicine, 33(5), 40-45 (1999-12-11)
Acute experiments with dogs showed that irritation of the sympathetic trunk in the thoracic cavity is more likely to amplify than inhibit duodenal contractions. This stimulating effect is better seen with alpha- and beta-adrenoreceptors blocked by phentolamine hydrochloride and inderal
Shinsuke Inuki et al.
Organic letters, 10(22), 5239-5242 (2008-10-30)
Ergot alkaloids and their synthetic analogs have been reported to exhibit broad biological activity. We investigated direct construction of the C/D ring system of ergot alkaloids based on palladium-catalyzed domino cyclization of amino allenes. With this biscyclization as the key
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