Home Other Building Blocks Lysergol

Lysergol

CAS No.:
602-85-7
Catalog Number:
AG00F2Z7
Molecular Formula:
C17H19NO
Molecular Weight:
253.3389
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
100mg
95%
In Stock USA
United States
$248
- +
500mg
95%
In Stock USA
United States
$554
- +
1g
95%
In Stock USA
United States
$901
- +
Product Description
Catalog Number:
AG00F2Z7
Chemical Name:
Lysergol
CAS Number:
602-85-7
Molecular Formula:
C17H19NO
Molecular Weight:
253.3389
MDL Number:
MFCD00010029
IUPAC Name:
[(6aR,9R)-7-methyl-6,6a,8,9-tetrahydro-4H-indolo[4,3-fg]quinolin-9-yl]methanol
InChI:
InChI=1S/C16H18N2O/c1-18-8-10(9-19)5-13-12-3-2-4-14-16(12)11(7-17-14)6-15(13)18/h2-5,7,10,15,17,19H,6,8-9H2,1H3/t10-,15-/m1/s1
InChI Key:
BIXJFIJYBLJTMK-MEBBXXQBSA-N
SMILES:
OC[C@@H]1CC(C)[C@@H]2C(=C1)c1cccc3c1c(C2)c[nH]3
EC Number:
210-024-5
UNII:
NTR684Z1AZ
Properties
Complexity:
394  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
2  
Defined Bond Stereocenter Count:
0
Exact Mass:
254.142g/mol
Formal Charge:
0
Heavy Atom Count:
19  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
254.333g/mol
Monoisotopic Mass:
254.142g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
39.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.2  
Literature
Title Journal
Simultaneous quantification of berberine and lysergol by HPLC-UV: evidence that lysergol enhances the oral bioavailability of berberine in rats. Biomedical chromatography : BMC 20121001
Quantitative determination of bioactive alkaloids lysergol and chanoclavine in Ipomoea muricata by reversed-phase high-performance liquid chromatography. Biomedical chromatography : BMC 20120901
Lysergol monohydrate. Acta crystallographica. Section E, Structure reports online 20120201
Changes in concentrations of lysergol in urine and prolactin in plasma, rectal temperature and respiration rate in sheep selected for resistance or susceptibility to ryegrass staggers and fed ergovaline. New Zealand veterinary journal 20110901
Profiling of a prescription drug library for potential renal drug-drug interactions mediated by the organic cation transporter 2. Journal of medicinal chemistry 20110714
Enantioselective total synthesis of (+)-lysergic acid, (+)-lysergol, and (+)-isolysergol by palladium-catalyzed domino cyclization of allenes bearing amino and bromoindolyl groups. The Journal of organic chemistry 20110401
Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis. Bioorganic & medicinal chemistry letters 20101101
Enantioselective synthesis of (+)-isolysergol via ring-closing metathesis. Organic letters 20100604
Large-scale separation of clavine alkaloids from Ipomoea muricata by pH-zone-refining centrifugal partition chromatography. Journal of chromatography. B, Analytical technologies in the biomedical and life sciences 20090615
Total synthesis of (+/-)-lysergic acid, lysergol, and isolysergol by palladium-catalyzed domino cyclization of amino allenes bearing a bromoindolyl group. Organic letters 20081120
Ergot alkaloids in Norwegian wild grasses: a mass spectrometric approach. Rapid communications in mass spectrometry : RCM 20070101
Detection of lysergic acid in ruminal fluid, urine, and in endophyte-infected tall fescue using high-performance liquid chromatography. Journal of veterinary diagnostic investigation : official publication of the American Association of Veterinary Laboratory Diagnosticians, Inc 20060701
Microsphere-based protease assays and screening application for lethal factor and factor Xa. Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501
Electrospray[+] tandem quadrupole mass spectrometry in the elucidation of ergot alkaloids chromatographed by HPLC: screening of grass or forage samples for novel toxic compounds. Journal of mass spectrometry : JMS 20051101
Fragmentation patterns of selected ergot alkaloids by electrospray ionization tandem quadrupole mass spectrometry. Journal of mass spectrometry : JMS 20041101
Ergot alkaloid transport across ruminant gastric tissues. Journal of animal science 20010201
Two amino acid differences in the sixth transmembrane domain are partially responsible for the pharmacological differences between the 5-HT1D beta and 5-HT1E 5-hydroxytryptamine receptors. Journal of neurochemistry 19961101
Human serotonin 1D receptor is encoded by a subfamily of two distinct genes: 5-HT1D alpha and 5-HT1D beta. Proceedings of the National Academy of Sciences of the United States of America 19920415
Substituted ergolines: potential antipsychotics with unique profile. I. Psychopharmacological characterization. Polish journal of pharmacology and pharmacy 19880101
Properties