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Key Documents

SML1349

Sigma-Aldrich

SB-207266

≥98% (HPLC)

Synonym(s):

1′-Butyl-4′-piperidinylmethyl ester, 8-Amino-7-chloro-2,3-dihydro-1,4-benzodioxan-5-carboxylic acid, N-1-Butyl-4-piperinylmethyl)-3,4-dihydro-2H-[1,3] oxazino[3,2-a]indole-10-carboxamide, Piboserod

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About This Item

Empirical Formula (Hill Notation):
C22H31N3O2
CAS Number:
Molecular Weight:
369.50
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.77

Quality Level

Assay

≥98% (HPLC)

form

powder

color

white to beige

solubility

DMSO: 5 mg/mL, clear (warmed)

storage temp.

2-8°C

SMILES string

O=C(NCC1CCN(CCCC)CC1)C2=C3N(CCCO3)C4=C2C=CC=C4

InChI

1S/C22H31N3O2/c1-2-3-11-24-13-9-17(10-14-24)16-23-21(26)20-18-7-4-5-8-19(18)25-12-6-15-27-22(20)25/h4-5,7-8,17H,2-3,6,9-16H2,1H3,(H,23,26)

InChI key

KVCSJPATKXABRQ-UHFFFAOYSA-N

Biochem/physiol Actions

SB-207266 is a potent, selective, orally active and long-acting 5-HT4 antagonist in vivo.

Pictograms

Skull and crossbones

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 3 Oral

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

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Barbora Waclawiková et al.
PLoS biology, 19(1), e3001070-e3001070 (2021-01-23)
Microbial conversion of dietary or drug substrates into small bioactive molecules represents a regulatory mechanism by which the gut microbiota alters intestinal physiology. Here, we show that a wide variety of gut bacteria can metabolize the dietary supplement and antidepressant

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