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N1134

Sigma-Aldrich

Se-(p-Nitrobenzyl)-6-selenoinosine

≥95%

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About This Item

Linear Formula:
C17H17SeN5O6
CAS Number:
40144-12-5
Molecular Weight:
466.31
MDL number:
MFCD00056966
UNSPSC Code:
41106305
PubChem Substance ID:
24897462

Assay

≥95%

form

solid

storage temp.

−20°C

SMILES string

OCC1OC(C(O)C1O)n2cnc3c([Se]Cc4ccc(cc4)N(=O)=O)ncnc23

InChI

1S/C17H17N5O6Se/c23-5-11-13(24)14(25)17(28-11)21-8-20-12-15(21)18-7-19-16(12)29-6-9-1-3-10(4-2-9)22(26)27/h1-4,7-8,11,13-14,17,23-25H,5-6H2

InChI key

XCNANXPIYMOXKW-UHFFFAOYSA-N

Biochem/physiol Actions

Se-(p-nitrobenzyl)-6-selenoinosine is a selenium containing inosine derivative that may have activities similar to S-(p-nitrobenzyl)-6-thioinosine (NBTI), an inhibitor of adenosine equilibrative transporters.

Signal Word

Danger

Hazard Statements

H301 + H331,H373,H410

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - STOT RE 2

Storage Class Code

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

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

PDSCL

Poisonous substance

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

N1134-5MG:4548173204079
N1134-1MG:4548173204055
N1134-BULK:
N1134-10MG:4548173204048
N1134-25MG:4548173204062
N1134-VAR:

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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M A Timóteo et al.
Neurochemistry international, 52(4-5), 834-845 (2007-11-21)
The influence of nerve stimulation pattern on transmitter release inhibition by L-citrulline, the co-product of NO biosynthesis by nitric oxide synthase (NOS), was studied in the rat phrenic nerve-hemidiaphragm. We also investigated the putative interactions between NOS pathway and the
Sílvia V Conde et al.
Journal of neurochemistry, 89(5), 1148-1156 (2004-05-19)
The effect of hypoxia on the release of adenosine was studied in vitro in the rat whole carotid body (CB) and compared with the effect of hypoxia (2%, 5% and 10% O(2)) on adenosine concentrations in superior cervical ganglia (SCG)
Alexandre dos Santos-Rodrigues et al.
Biochemical and biophysical research communications, 414(1), 175-180 (2011-09-29)
Adenosine is an important modulator of neuronal survival and differentiation in the CNS. Our previous work showed that nucleoside transporters (NTs) are present in cultures of chick retinal cells, but little is known about the mechanisms regulating adenosine transport in
Laura Oliveira et al.
Neuroscience letters, 459(3), 127-131 (2009-05-12)
At the rat motor nerve terminals, activation of muscarinic M(1) receptors negatively modulates the activity of inhibitory muscarinic M(2) receptors. The present work was designed to investigate if the negative crosstalk between muscarinic M(1) and M(2) autoreceptors involved endogenous adenosine

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