6-Aminoseleno-D-luciferin
Code | Size | Price |
---|
CDX-A0307-M001 | 1 mg | £267.00 |
Quantity:
CDX-A0307-M005 | 5 mg | £792.00 |
Quantity:
Prices exclude any Taxes / VAT
Overview
Regulatory Status: RUO
Shipping:
Ambient
Storage:
+4 °C
Images
Documents
Further Information
Alternate Names/Synonyms:
(4S)-2-(6-Amino-2-benzothiazolyl)-4,5-dihydro-4-delenazolecarboxylic acid
Appearance:
Dark brown solid.
CAS:
1375964-28-5
EClass:
32160000
Form (Short):
liquid
GHS Symbol:
GHS07
Handling Advice:
Keep cool and dry.Protect from light and moisture.
InChi:
InChI=1S/C11H9N3O2SSe/c12-5-1-2-6-8(3-5)17-9(13-6)10-14-7(4-18-10)11(15)16/h1-3,7H,4,12H2,(H,15,16)
InChiKey:
AQIRXTPMSNSUTJ-UHFFFAOYSA-N
Long Description:
Chemical. CAS: 1375964-28-5. Formula: C11H9N3O2SSe. MW: 326.23. Synthetic. Firefly luciferase substrate. Selenium analog of firefly L-luciferin with red-shifted bioluminescence emission for use in in vivo bioluminescence imaging. Bioluminescence spectra: max. 600nm. This selenium analog exhibits a similar substrate affinity to wild type D-luciferin, though with slightly lower quantum yield.
MDL:
MFCD31656727
Molecular Formula:
C11H9N3O2SSe
Molecular Weight:
326.23
Package Type:
Vial
Product Description:
Firefly luciferase substrate. Selenium analog of firefly L-luciferin with red-shifted bioluminescence emission for use in in vivo bioluminescence imaging. Bioluminescence spectra: max. 600nm. This selenium analog exhibits a similar substrate affinity to wild type D-luciferin, though with slightly lower quantum yield.
Purity:
>90% (HPLC)
Signal word:
Warning
SMILES:
NC1=CC=C2C(SC(C3=N[C@@H](C(O)=O)C[Se]3)=N2)=C1
Solubility Chemicals:
Soluble in water or PBS (10mg/ml).
Source / Host:
Synthetic.
Transportation:
Non-hazardous
UNSPSC Category:
Fluorescent Reagents
UNSPSC Number:
41105331
Use & Stability:
Stable for at least 2 years after receipt when stored at -20°C.
References
(1) N.R. Conley, et al.; Angew. Chem. Int. Ed. Engl. 51, 3350 (2012) | (2) D.M. Mofford, et al.; JACS 136, 13277 (2014) | (3) S.T. Adams & S.C. Miller; Curr. Opin. Chem. Biol. 21, 112 (2014)
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