1 | D-Tryptophan |
2 | H-D-Trp-OH |
3 | (R)-Tryptophan |
4 | D-TRYPTOPHANE |
5 | D(+)-Tryptophan |
D-tryptophan is the D-enantiomer of tryptophan. It has a role as a bacterial metabolite. It is a tryptophan and a D-alpha-amino acid. It is a conjugate base of a D-tryptophanium. It is a conjugate acid of a D-tryptophanate. It is an enantiomer of a L-tryptophan. It is a tautomer of a D-tryptophan zwitterion.
Molecular Formula | C11H12N2O2 |
---|---|
Canonical SMILES | C1=CC=C2C(=C1)C(=CN2)CC(C(=O)O)N |
Isomeric SMILES | C1=CC=C2C(=C1)C(=CN2)C[C@H](C(=O)O)N |
Molecular Weight | 204.2200 |
InChIKey | QIVBCDIJIAJPQS-SECBINFHSA-N |
InChI | InChI=1S/C11H12N2O2/c12-9(11(14)15)5-7-6-13-10-4-2-1-3-8(7)10/h1-4,6,9,13H,5,12H2,(H,14,15)/t9-/m1/s1 |
XLogP | -1.1000 |
ExactMass | 204.0899 |
MonoisotopicMass | 204.0899 |
TPSA | 79.1000 |
Complexity | 245.0000 |
Charge | 0.0000 |
HBondDonorCount | 3 |
HBondAcceptorCount | 3 |
RotatableBondCount | 3 |
HeavyAtomCount | 15 |
IsotopeAtomCount | 0 |
AtomStereoCount | 1 |
DefinedAtomStereoCount | 1 |
UndefinedAtomStereoCount | 0 |
BondStereoCount | 0 |
DefinedBondStereoCount | 0 |
UndefinedBondStereoCount | 0 |
CovalentUnitCount | 1 |
PatentCount | 37210 |
PatentFamilyCount | 14589 |
LiteratureCount | 1338 |