Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
89
datasets available to search
ShareScore release 0.9.0
Dataset results
89 results for “chlorine”
A Clinical Trial to Assess the Effects of a Mouthwash Containing Chlorine Dioxide on Oral Malodor
ClinicalTrials.gov study NCT00655772. IPD Sharing: Not stated. Countries: 1. Publications: 1.
Airway Dysfunction and Remodelling in Athletes Following Swimming Training in Chlorinated Pools
ClinicalTrials.gov study NCT00686452. IPD Sharing: Not stated. Countries: 1. Publications: 2.
Determination of the Effectiveness of Oral Chlorine Dioxide in the Treatment of COVID 19
ClinicalTrials.gov study NCT04343742. IPD Sharing: UNDECIDED. Countries: 1. Publications: 5.
Drinking Water Chlorination and Child Survival in Rural Kenya
ClinicalTrials.gov study NCT04020965. IPD Sharing: Not stated. Countries: 1. Publications: 1.
Data from: Nitrogen and chlorine co-doped carbon dots as probe for sensing and imaging in biological samples
A facile one step hydrothermal synthesis approach was proposed to prepare nitrogen and chlorine co-doped carbon dots using l-ornithine hydrochloride as the sole precursor. The configuration and component of carbon dots were characterized by TEM, XPS, and FTIR. The obtained CDs (Orn-CDs) with a mean diameter of 2.1 nm were well monodispersed in aqueous solutions. The as-prepared CDs exhibited a bright blue fluorescence with a high yield of 60%, good photostability and low cytotoxicity. The emission of Orn-CDs could be selectively and effectively suppressed by Fe3+. Thus, a quantitative assay of Fe3+ was realized by this nanoprobe with a detection limit of 95.6 nmol L-1 in the range of 0.3-50 µmol L-1. Furthermore, ascorbic acid could recover the fluorescence of Orn-CDs suppressed by Fe3+, owing to the transformation of Fe3+ to Fe2+ by ascorbic acid. The limit of detection for ascorbic acid was 137 nmol L-1 in the range of 0.5-10 µmol L-1. In addition, the established method was successfully applied for Fe3+ and ascorbic acid sensing in human serum and urine specimans and for imaging of Fe3+ in living cells. With merits of low economic cost, easy to scale up, without additional functionalized and sample pretreatment, Orn-CDs based sensing platform showed its potential to be used for biomedical related study.
The impact of chlorine chemistry combined with heterogeneous N2O5 reactions on air quality in China
<p>This is the revised GEOS-Chem code for all sensitivity simulations in the paper.</p>
Table 5 in The grass root endophytic fungus Flavomyces fulophazii: An abundant source of tetramic acid and chlorinated azaphilone derivatives
<p><b>Table 5</b> NMR data of flavochlorine A (compound <b>7</b>) and flavochlorine G (compound <b>10</b>) in methanol- <i>d</i> 4.</p><table><tbody><tr><th>No. a</th><th>flavochlorine A</th><th></th><th>flavochlorine G</th><th></th></tr></tbody><tbody><tr><th></th><td><i>δ</i> H</td><td><i>δ</i> C</td><td><i>δ</i> H</td><td><i>δ</i> C</td></tr><tr><th>1</th><td>8.795, <i>s,</i> 1H</td><td>140.8</td><td>8.80, s, 1H</td><td>141.3</td></tr><tr><th>3</th><td>–</td><td>147.5</td><td>–</td><td>145.9</td></tr><tr><th>4</th><td>7.51, <i>s</i>, 1H</td><td>114.0</td><td>7.49, s, 1H</td><td>115.2</td></tr><tr><th>4a</th><td>–</td><td>146.9</td><td></td><td>146.9</td></tr><tr><th>5</th><td>–</td><td>106.8</td><td></td><td>106.7</td></tr><tr><th>6</th><td>–</td><td>174.8</td><td></td><td>174.6</td></tr><tr><th>7</th><td>6.44, <i>s,</i> 1H</td><td>106.6</td><td>6.45, s, 1H</td><td>106.0</td></tr><tr><th>8</th><td>–</td><td>157.9</td><td>–</td><td>158.4</td></tr><tr><th>8a</th><td>–</td><td>107.1</td><td>–</td><td>107.8</td></tr><tr><th>9</th><td>2.95, <i>t</i>, (7.9), 2H</td><td>35.3</td><td>2.90, t (7.6), 2H</td><td>33.62</td></tr><tr><th>10</th><td>1.80, <i>m</i>, 2H</td><td>22.8</td><td>1.80, m, 2H</td><td>21.95</td></tr><tr><th>11</th><td>1.11, <i>t</i>, (7.4), 3H</td><td>13.6</td><td>1.10, t, (6.9), 3H</td><td>12.90</td></tr><tr><th>1′</th><td>4.43, <i>t</i>, (5.0), 2H</td><td>57.5</td><td>4.32, t (7,3), 1H</td><td>54.49</td></tr><tr><th>2′</th><td>3.91, <i>t</i>, (5.0), 2H</td><td>61.6</td><td>2.24, m, 2H</td><td>34.22</td></tr><tr><th>3′</th><td>–</td><td>–</td><td>3.25, m, 2H</td><td>48.21</td></tr><tr><th>4′</th><td>–</td><td>–</td><td>1.31, d, (7.0), 3H</td><td>20.97</td></tr><tr><th>5′</th><td></td><td></td><td>–</td><td>176.3</td></tr><tr><th>O–Me</th><td>3.96, <i>s,</i> 3H</td><td>56.4</td><td>3.95, s, 3H</td><td>55.46</td></tr></tbody></table><p><sup>a</sup> Corresponding numbered molecular structures are found in Fig. 3.</p>
Table 2 in The grass root endophytic fungus Flavomyces fulophazii: An abundant source of tetramic acid and chlorinated azaphilone derivatives
<p><b>Table 2</b> High resolution mass-spectral (positive ion mode) data for compounds detected in Flavomyces fulophazii culture extracts.</p><table><tbody><tr><th>Compound</th><th></th><th>Formula</th><th>Detected ion</th><th>Detected formula</th><th>Calculated <i>m/z</i></th><th>Found <i>m/z</i></th><th>diff (ppm)</th></tr></tbody><tbody><tr><th>No. a</th><td>Name</td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>1</th><td>10,11-dihydroxy-vermelhotin</td><td>C12H13O5N</td><td>[M+H]+</td><td>C12H14O5N</td><td>252.0866</td><td>252.0865</td><td>0.472</td></tr><tr><th></th><td></td><td></td><td>[M+Na]+</td><td>C12H13O5NNa</td><td>274.0686</td><td>274.0684</td><td>0.853</td></tr><tr><th>2</th><td>11-hydroxy-vermelhotin</td><td>C12H13O4N</td><td>[M+H]+</td><td>C12H14O4N</td><td>236.0917</td><td>236.0915</td><td>0.908</td></tr><tr><th></th><td></td><td></td><td>[M+Na]+</td><td>C12H13O4NNa</td><td>258.0737</td><td>258.0735</td><td>0.500</td></tr><tr><th>3</th><td>11-oxo-vermelhotin</td><td>C12H11O4N</td><td>[M+H]+</td><td>C12H12O4N</td><td>234.0761</td><td>234.0758</td><td>1.129</td></tr><tr><th></th><td></td><td></td><td>[M+Na]+</td><td>C12H11O4NNa</td><td>256.0580</td><td>256.0577</td><td>1.363</td></tr><tr><th>4</th><td>11-methoxy-vermelhotin</td><td>C13H15O4N</td><td>[M+H]+</td><td>C13H16O4N</td><td>250.1074</td><td>250.1072</td><td>0.698</td></tr><tr><th></th><td></td><td></td><td>[M+Na]+</td><td>C13H15O4NNa</td><td>272.0893</td><td>272.0890</td><td>1.136</td></tr><tr><th>5</th><td>vermelhotin</td><td>C12H11O3N</td><td>[M+H]+</td><td>C12H12O3N</td><td>218.0812</td><td>218.0809</td><td>1.145</td></tr><tr><th></th><td></td><td></td><td>[M+Na]+</td><td>C12H11O3NNa</td><td>240.0631</td><td>240.0628</td><td>1.351</td></tr><tr><th>6a</th><td>flavochlorine E</td><td>C16H18O5NCl</td><td>[M+H]+</td><td>C H O NCl35 16 19 5</td><td>340.0946</td><td>340.0944</td><td>0.785</td></tr><tr><th></th><td></td><td></td><td>[M + H+2]+</td><td>C H O NCl37 16 19 5</td><td>342.0917</td><td>342.0912</td><td>1.335</td></tr><tr><th>6b</th><td>flavochlorine F</td><td>C16H18O5NCl</td><td>[M+H]+</td><td>C H O NCl35 16 19 5</td><td>340.0946</td><td>340.0944</td><td>0.696</td></tr><tr><th></th><td></td><td></td><td>[M + H+2]+</td><td>C H O NCl37 16 19 5</td><td>342.0917</td><td>342.0913</td><td>1.160</td></tr><tr><th>7</th><td>flavochlorine A</td><td>C15H18O3NCl</td><td>[M+H]+</td><td>C H O NCl35 15 19 3</td><td>296.1048</td><td>296.1045</td><td>1.039</td></tr><tr><th></th><td></td><td></td><td>[M + H+2]+</td><td>C H O NCl37 15 19 3</td><td>298.1018</td><td>298.1016</td><td>0.763</td></tr><tr><th>8</th><td>flavochlorine B</td><td>C13H14O2NCl</td><td>[M+H]+</td><td>C H O NCl35 13 15 2</td><td>252.0786</td><td>252.0783</td><td>1.162</td></tr><tr><th></th><td></td><td></td><td>[M + H+2]+</td><td>C H O NCl37 13 15 2</td><td>254.0756</td><td>254.0753</td><td>1.310</td></tr><tr><th>9</th><td>flavochlorine C</td><td>C16H20O3NCl</td><td>[M+H]+</td><td>C H O NCl35 16 21 3</td><td>310.1204</td><td>310.1202</td><td>0.863</td></tr><tr><th></th><td></td><td></td><td>[M + H+2]+</td><td>C H O NCl37 16 21 3</td><td>312.1175</td><td>312.1171</td><td>1.178</td></tr><tr><th>10</th><td>flavochlorine G</td><td>C18H22O4NCl</td><td>[M+H]+</td><td>C H O NCl35 18 23 4</td><td>352.1310</td><td>352.1307</td><td>0.859</td></tr><tr><th></th><td></td><td></td><td>[M + H+2]+</td><td>C H O NCl37 18 23 4</td><td>354.1281</td><td>354.1276</td><td>1.418</td></tr><tr><th>11</th><td>flavochlorine D</td><td>C13H13O3Cl</td><td>[M+H]+</td><td>C H O Cl35 13 14 3</td><td>253.0626</td><td>253.0622</td><td>1.417</td></tr><tr><th></th><td></td><td></td><td>[M + H+2]+</td><td>C H O Cl37 13 14 3</td><td>255.0596</td><td>255.0593</td><td>1.444</td></tr></tbody></table><p><sup>a</sup> Numbers of compounds correspond to those in Figs. 2 and 3.</p>
Table 6 in The grass root endophytic fungus Flavomyces fulophazii: An abundant source of tetramic acid and chlorinated azaphilone derivatives
<p><b>Table 6</b> Antiproliferative activity of vermelhotin, hydroxyvermelhotin and flavochlorine A isolated from <i>Flavomyces fulophazii</i> culture extracts.</p><table><tbody><tr><th>Cell line</th><th>Antiproliferative activity (IC50, μM)</th><th></th><th></th></tr></tbody><tbody><tr><th></th><td>vermelhotin</td><td>hydroxy-</td><td>flavochlorine</td><td>reference a</td></tr><tr><th></th><td></td><td>vermelhotin</td><td>A</td><td>Dau</td><td>Sal</td></tr><tr><th>A2058</th><td>12.1</td><td><i>></i> 100</td><td>67.9</td><td>0.3 1</td><td></td></tr><tr><th>HepG2</th><td>10.1</td><td><i>></i> 100</td><td><i>></i> 100</td><td>1.2 2</td><td>5.8 3</td></tr><tr><th>A431</th><td>19.9</td><td><i>></i> 100</td><td><i>></i> 100</td><td>0.7</td><td></td></tr><tr><th>U87</th><td>28.6</td><td><i>></i> 100</td><td><i>></i> 100</td><td>0.4 2</td><td>0.8</td></tr><tr><th>EBC-1</th><td>20.0</td><td><i>></i> 100</td><td><i>></i> 100</td><td>1.2</td><td></td></tr><tr><th>SH-SY5Y</th><td>12.9</td><td><i>></i> 100</td><td><i>></i> 100</td><td>0.7</td><td></td></tr><tr><th>HT-29</th><td>31.4</td><td><i>></i> 100</td><td><i>></i> 100</td><td>0.2 4</td><td></td></tr><tr><th>HL-60</th><td>9.4</td><td><i>></i> 100</td><td><i>></i> 100</td><td>0.02 5</td><td></td></tr><tr><th>MonoMac-</th><td>17.1</td><td><i>></i> 100</td><td><i>></i> 100</td><td>0.6</td><td>2.2 3</td></tr><tr><th>6</th><td></td><td></td><td></td><td></td><td></td></tr><tr><th>LCLC-</th><td>37.0</td><td><i>></i> 100</td><td><i>></i> 100</td><td>8.6</td><td></td></tr><tr><th>103H</th><td></td><td></td><td></td><td></td><td></td></tr><tr><th>HEK-293</th><td>21.6</td><td><i>></i> 100</td><td><i>></i> 100</td><td>no</td><td></td></tr><tr><th></th><td></td><td></td><td></td><td>data</td><td></td></tr><tr><th>H838</th><td>22.1</td><td><i>></i> 100</td><td><i>></i> 100</td><td>10.2</td><td></td></tr><tr><th>VERO</th><td><i>></i> 100</td><td><i>></i> 100</td><td><i>></i> 100</td><td>no</td><td></td></tr><tr><th></th><td></td><td></td><td></td><td>data</td><td></td></tr></tbody></table>
Fig. 5 in Chlorine-containing guaianolide sesquiterpenoids from Achillea millefolium L. with inhibitory effects against LPS-induced NO release in BV-2 microglial cells
Fig. 5. ORTEP diagrams of compounds 1, 4, 6 and 8.
Fig. 3. Key 1 H– 1 H in Chlorine-containing guaianolide sesquiterpenoids from Achillea millefolium L. with inhibitory effects against LPS-induced NO release in BV-2 microglial cells
Fig. 3. Key 1 H– 1 H COSY, HMBC, and NOESY correlations of compound 6.
Fig. 1 in Chlorine-containing guaianolide sesquiterpenoids from Achillea millefolium L. with inhibitory effects against LPS-induced NO release in BV-2 microglial cells
Fig. 1. Structures of Millefolactons B1–B9 (1–9) isolated from A. millefolium L.
Fig. 4 in Chlorine-containing guaianolide sesquiterpenoids from Achillea millefolium L. with inhibitory effects against LPS-induced NO release in BV-2 microglial cells
Fig. 4. Experimental ECD spectra of compounds 1–9.
Fig. 2. Key 1H–1H in Chlorine-containing guaianolide sesquiterpenoids from Achillea millefolium L. with inhibitory effects against LPS-induced NO release in BV-2 microglial cells
Fig. 2. Key 1H–1H COSY, HMBC, and NOESY correlations of compound 1.
Clinical and Microbiological Effects of a Mouthwash Containing Chlorine Dioxide
ClinicalTrials.gov study NCT00748943. IPD Sharing: Not stated. Countries: 0. Publications: 1.
The Efficacy of Stabilized Chlorine Dioxide Rinse as a Chemical Adjuvant for Treatment of Per-implant Mucositis
ClinicalTrials.gov study NCT04838054. IPD Sharing: NO. Countries: 1. Publications: 0.
Data from: Nitrogen and chlorine co-doped carbon dots as probe for sensing and imaging in biological samples
Open the record for dataset details and reuse information.
MLS/Aura Level 3 Daily Binned Chlorine Monoxide (ClO) Mixing Ratio on Zonal and Similar Grids V004 (ML3DZCLO) at GES DISC
ML3DZCLO is the EOS Aura Microwave Limb Sounder (MLS) daily binned on zonal and assorted vertical grids product for chlorine monoxide (ClO) derived from radiances measured primarily by the 640 GHz radiometer. The data version is 4.2. Data coverage is from August 2, 2004 to current. Spatial coverage is near-global (-82 to +82 degrees latitude) at 4 degree latitude zonal increments. The recommended useful vertical range is between 147 and 1.0 hPa, and the vertical resolution varies between 3 and 4.5 km. Users of the ML3DZCLO data product should read chapter 4 and section 3.6 of the EOS MLS Level 2 Version 4 Quality Document for more information.The data files contain one year of data and are archived in the netCDF4 format, which is also compatible with HDF5 readers and tools. Each file contains four group objects: lat vs pressure zonal mean, lat vs "potential temperature" zonal mean, "equivalent latitude" vs "potential temperature" zonal mean, and vortex average vs "potential temperature". These are further subdivided into groups with all valid, ascending orbit, descending orbit, daytime (SZA < 90), and nighttime (SZA > 110) profiles. Each group has a set of data (average, min, max, std dev, rms) and geolocation fields, grid attributes, and metadata.
HIRDLS/Aura Level 3 Chlorine Nitrate (ClONO2) 1deg Lat Zonal Fourier Coefficients V007 (H3ZFCCLONO2) at GES DISC
The "HIRDLS/Aura Level 3 Chlorine Nitrate (ClONO2) Zonal Fourier Coefficients" version 7 data product (H3ZFCCLONO2) contains the entire mission (~3 years) of HIRDLS data expressed as zonal Fourier coefficients in 1 degree latitude bands from -64 to 80 degrees at 121 pressure levels. The coefficients are computed from the HIRDLS Level 2 profiles with a Kalman filter approach using both forward and backward passes in time. Expressed as the mean and up to 7 sine and cosine coefficients (4 waves for ascending and descending, 7 waves for combined), these coefficients may be used to compute values at any longitude. The data are provided on a pressure grid with 24 levels per decade, corresponding to about 1 km vertical resolution. The useful vertical range of the data is 100 to 1.0 hPa. The precision values are given by the root-mean square of the differences between the estimated fields and the input data.The data are stored in the version 5 Hierarchical Data Format for the Earth Observing System (HDF-EOS5), which is an extension of the HDF5 format. Each file contains a zonal object with data for the entire mission with separate data fields for ascending (daytime), descending (nighttime), and combined orbit node.
OMI/Aura Chlorine Dioxide (OClO) Total Column 1-orbit L2 Swath 13x24 km V003 (OMOCLO) at GES DISC
The Aura Ozone Monitoring Instrument (OMI) collection-3 Chlorine Dioxide Product OMOCLO is now available from the NASA Goddard Earth Sciences Data and Information Services Center (GES DISC) for public access. The shortname for this Level-2 OMI total column OClO product is OMOCLO. The algorithm leads for this product are the US OMI scientists Dr. Kelly Chance and Dr. Thomas Kurosu from the Harvard-Smithsonian Center, Cambridge, MA. The OMOCLO product contains slant column OClO, standard errors (rms and sigma), quality flags, geolocation and other ancillary information.The OMOCLO files are stored in the version 5 EOS Hierarchical Data Format (HDF-EOS5). Each file contains data from the day lit portion of an orbit (~53 minutes). There are approximately 14 orbits per day. The maximum file size for the OMOCLO data product is about 20 MB.
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.