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Key Documents

S1068

Sigma-Aldrich

SB-215505

solid, >98% (HPLC)

Synonym(s):

6-Chloro-5-methyl-1-5-quinolycarbamoyl-indoline

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About This Item

Empirical Formula (Hill Notation):
C19H16N3OCl
CAS Number:
Molecular Weight:
337.80
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.77

Assay

>98% (HPLC)

form

solid

color

off-white

solubility

DMSO: soluble ~11 mg/mL at 60 °C
H2O: insoluble

originator

GlaxoSmithKline

storage temp.

2-8°C

SMILES string

Cc1cc2CCN(C(=O)Nc3ccnc4ccccc34)c2cc1Cl

InChI

1S/C19H16ClN3O/c1-12-10-13-7-9-23(18(13)11-15(12)20)19(24)22-17-6-8-21-16-5-3-2-4-14(16)17/h2-6,8,10-11H,7,9H2,1H3,(H,21,22,24)

InChI key

BPVGSWDWIRIUME-UHFFFAOYSA-N

Gene Information

human ... HTR2B(3357)

Biochem/physiol Actions

Selective 5-HT2B serotonin receptor antagonist; 100-fold higher affinity at 2B versus 2C.

Features and Benefits

This compound was developed by GlaxoSmithKline. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.

Legal Information

Sold for research purposes under agreement from Glaxo­Smith­Kline

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Adam J Isabella et al.
Developmental cell, 53(3), 344-357 (2020-04-18)
Information flow through neural circuits often requires their organization into topographic maps in which the positions of cell bodies and synaptic targets correspond. To understand how topographic map development is controlled, we examine the mechanism underlying targeting of vagus motor

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