6-Chlorotryptophan

HCID 65259CAS 17808-21-8
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Basic information

Standard SMILES
NC(Cc1c[nH]c2cc(Cl)ccc12)C(=O)O
InChIKey
FICLVQOYKYBXFN-UHFFFAOYSA-N
Molecular formula
C11H11ClN2O2
Average molar mass
238.67 g/mol
Monoisotopic mass
238.05090527

Overview

6-chlorotryptophan is a tryptophan derivative that is tryptophan in which the hydrogen at position 6 of the indole ring has been replaced by a chlorine. It is a tryptophan derivative, an organochlorine compound and a non-proteinogenic alpha-amino acid.

Names & identifiers

Preferred name
6-Chlorotryptophan
IUPAC
2-amino-3-(6-chloro-1H-indol-3-yl)propanoic acid
English name
6-chlorotryptophan
Molecular weight
0

Names & synonyms

6-ChlorotryptophanCHEBI:140516DTXSID7093903017808-35-4RefChem:913898DTXCID90136754117808-21-86-chloro-dl-tryptophan2-amino-3-(6-chloro-1H-indol-3-yl)propanoic acid6-Chloro-D,L-tryptophanrac-6-ChlorotryptophanDL-6-Chlorotryptophane
Show more names
DL-Tryptophan, 6-chloro-MFCD00152036H-Trp(6-Cl)-OHH-DL-Trp(6-Cl)-OHTryptophan, 6-chloro-TC49834B5Ddl-6-chlorotryptophan6-Chloro (R)-Tryptophan

Database identifiers

CAS
17808-21-8、17808-35-4
PubChem CID
65259
DTXSID
DTXSID70939030
ChEBI
CHEBI:140516
UNII
TC49834B5D

Properties

Computed structural properties

XLogP
-0.3
Topological polar surface area
79.1 Ų
Hydrogen bond donors
3
Hydrogen bond acceptors
3
Rotatable bonds
3
Heavy atoms
16

Experimental & physicochemical properties

Melting Point278 °C
Physical DescriptionSolid

Chemistry & industry

Pharmacology

Cellular LocationsCytoplasm

Suppliers40 total

陕西科贝莱药物研发有限公司13119135307 · [email protected]
毕佳索（上海毕得医药科技股份有限公司）400-6005915 · [email protected]
上海毕得医药科技股份有限公司400-1647117 13681763483 · [email protected]
江苏艾康生物医药研发有限公司025-66061636 19370895928 · [email protected]
北京索莱宝科技有限公司010-50973130 17801761073 · [email protected]
Additional notes · 1 item

DefinitionChEBI: 6-chlorotryptophan is a tryptophan derivative that is tryptophan in which the hydrogen at position 6 of the indole ring has been replaced by a chlorine. It is a tryptophan derivative, a non-proteinogenic alpha-amino acid and an organochlorine compound.

Related reactions

5 records
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Linked notes

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