D2938
4,5-Diaminofluorescein-Isopropanol adduct (1:2)
powder
Synonym(s):
4,5-Diaminofluorescein, DAF-2
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About This Item
Linear Formula:
C20H14N2O5 · 2C3H8O
CAS Number:
Molecular Weight:
482.53
MDL number:
UNSPSC Code:
12171500
PubChem Substance ID:
NACRES:
NA.47
Pricing and availability is not currently available.
Assay
≥98% (HPLC)
form
powder
application(s)
diagnostic assay manufacturing
hematology
histology
storage temp.
room temp
SMILES string
CC(C)O.CC(C)O.Nc1cc2C(=O)OC3(c4ccc(O)cc4Oc5cc(O)ccc35)c2cc1N
InChI
1S/C20H14N2O5.2C3H8O/c21-15-7-11-14(8-16(15)22)20(27-19(11)25)12-3-1-9(23)5-17(12)26-18-6-10(24)2-4-13(18)20;2*1-3(2)4/h1-8,23-24H,21-22H2;2*3-4H,1-2H3
InChI key
USEFIEWGHVUNEC-UHFFFAOYSA-N
Application
Fluorescent detector of nitric oxide in culture medium, tissue sections and biopsy cells
Formula variant
isopropanol adduct
Legal Information
DAF-2 is manufactured by Daiichi Pure Chemicals Co., LTD.
US Patent No. 5,874,590
US Patent No. 5,874,590
Storage Class Code
11 - 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
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Kazuki Sato et al.
SpringerPlus, 3, 274-274 (2014-10-04)
The Gram-negative bacterium Photorhabdus luminescens which symbiotically associates with the entomopathogenic nematode Heterorhabditis bacteriophora, has a broad insecticidal and nematicidal activity. The virulence of P. luminescens toward the non-mutualistic nematode Caenorhabditis elegans has not been described. We showed that when
Isabella Echeverri et al.
American journal of human biology : the official journal of the Human Biology Council, 27(6), 822-831 (2015-05-07)
To evaluate the Relationship between maternal and newborn endothelial function and oxidative stress. Forty-three pregnant women and their offspring were evaluated. As markers of endothelial function, the flow-mediated dilation (FMD) was measured in pregnant women in the second and third
Jae Sue Choi et al.
Archives of pharmacal research, 37(10), 1354-1363 (2014-07-06)
To investigate the effect of C-glycosylation at different positions of luteolin, the structure-activity relationships of luteolin and a pair of isomeric C-glycosylated derivatives orientin and isoorientin, were evaluated. We investigated the effects of C-glycosylation on the antioxidant, anti-Alzheimer's disease (AD)
Marta Rogowska et al.
Natural product communications, 10(11), 1825-1828 (2016-01-12)
The aim of the study was to determine the scavenging capacity of aqueous and ethanolic extracts derived from the herb of two species of Galinsoga against NO and ONOO-. In both tests the aqueous extracts of both Galinsoga species were
Naira Poerner Rodrigues et al.
Journal of agricultural and food chemistry, 63(19), 4815-4826 (2015-04-25)
The influence of green coffee genotype on the bioactive compounds and the in vitro antioxidant capacity against the principal reactive oxygen (ROO(•), H2O2, HO(•), and HOCl) and nitrogen (NO(•) and ONOO(-)) species of biological relevance was investigated. This is the
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