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Home Other Building Blocks 4-Methoxy-L-tryptophan

4-Methoxy-L-tryptophan

CAS No.:
406938-53-2
Catalog Number:
AG00CNJS
Molecular Formula:
Molecular Weight:
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Product Description
Catalog Number:
AG00CNJS
Chemical Name:
4-Methoxy-L-tryptophan
CAS Number:
406938-53-2
IUPAC Name:
(2S)-2-amino-3-(4-methoxy-1H-indol-3-yl)propanoic acid
InChI:
InChI=1S/C12H14N2O3/c1-17-10-4-2-3-9-11(10)7(6-14-9)5-8(13)12(15)16/h2-4,6,8,14H,5,13H2,1H3,(H,15,16)/t8-/m0/s1
InChI Key:
VYXPKRIKQJEAOO-QMMMGPOBSA-N
Properties
Complexity:
285  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Defined Bond Stereocenter Count:
0
Exact Mass:
234.1g/mol
Formal Charge:
0
Heavy Atom Count:
17  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0
Molecular Weight:
234.255g/mol
Monoisotopic Mass:
234.1g/mol
Rotatable Bond Count:
4  
Topological Polar Surface Area:
88.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-1.2  
Literature
Title Journal
General approach to the total synthesis of 9-methoxy-substituted indole alkaloids: synthesis of mitragynine, as well as 9-methoxygeissoschizol and 9-methoxy-N(b)-methylgeissoschizol. The Journal of organic chemistry 20090102
Total synthesis of the opioid agonistic indole alkaloid mitragynine and the first total syntheses of 9-methoxygeissoschizol and 9-methoxy-Nb-methylgeissoschizol. Organic letters 20070830
Argyrins, immunosuppressive cyclic peptides from myxobacteria. II. Structure elucidation and stereochemistry. The Journal of antibiotics 20020801
Total synthesis of the cyclic heptapeptide Argyrin B: a new potent inhibitor of T-cell independent antibody formation. Organic letters 20020307
Properties