Trp

Esters []
Tryptophan benzoate

Molecular structure via molpic
Conformer structure via 3Dmol.js
Molecular formula	C11H12N2O2
Molecular mass	204.22 g/mol
Predicted LogP	-1.1
Melting point	293 °C
Boiling point	289.00 to 291.00 °C. @ 760.00 mm Hg
Chirality	racemic

Identifiers []
IUPAC name	2-amino-3-(1H-indol-3-yl)propanoic acid
SMILES	C1=CC=C2C(=C1)C(=CN2)CC(C(=O)O)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)
InChIKey	QIVBCDIJIAJPQS-UHFFFAOYSA-N

Dosing

Oral []
Threshold	1 - 50 mg
Light	50 - 100 mg
Common	100 mg
Strong	100 - 250 mg
Heavy	250 - 400 mg

Statistically derived dosages by Sernyl

Tryptophan

(Redirected from L-Tryptophan)

Tryptophan (also known as DL-Tryptophan, (+-)-Tryptophan, Tryptophan, DL, Tryptophan, dl-, CCRIS 719, AI3-24395, Dl-tryptophan, DLTrytophane, DL3βIndolylalanine or DLαAmino3indolepropionic acid) is a substance of the tryptamine class.

Chemistry

Tryptophan is typically found in the form of its benzoate ester.

Stereochemistry

Stereoisomers []
(+)-Tryptophan	(-)-Tryptophan

See also

• Tryptamine
• Substituted tryptamines
• Bluedark

External links

• Tryptophan (Wikipedia)
• Tryptophan / (+)-Tryptophan / (-)-Tryptophan (Wikidata)
• Tryptophan / (+)-Tryptophan / (-)-Tryptophan (PubChem)
• Tryptophan / (+)-Tryptophan / (-)-Tryptophan (ChEMBL)
• Tryptophan / (+)-Tryptophan / (-)-Tryptophan (ChEBI)
• Tryptophan / (+)-Tryptophan (Common Chemistry)
• Tryptophan / (+)-Tryptophan / (-)-Tryptophan (HMDB)
• Tryptophan / (+)-Tryptophan / (-)-Tryptophan (KEGG)
• Tryptophan / (+)-Tryptophan / (-)-Tryptophan (UNII)
• Tryptophan / (+)-Tryptophan / (-)-Tryptophan (EPA DSSTox)