(2,4,6-Trichloro-phenoxy)-acetic acid (1H-pyrrol-2-ylmethylene)-hydrazide
(2,4,6-Trichloro-phenoxy)-acetic acid (1H-pyrrol-2-ylmethylene)-hydrazide Basic information
- Product Name:
- (2,4,6-Trichloro-phenoxy)-acetic acid (1H-pyrrol-2-ylmethylene)-hydrazide
- Synonyms:
-
- (2,4,6-Trichloro-phenoxy)-acetic acid (1H-pyrrol-2-ylmethylene)-hydrazide
- ML239
- NVEDPFICKAIHKD-NGYBGAFCSA-N
- ML239【(E)-N'-((1H-pyrrol-2-yl)methylene)-2-(2,4,6-trichlorophenoxy)acetohydrazide】
- CID 49843203
- CID49843203
- CID-49843203
- CID-49843203;CID 49843203;CID49843203;ML-239;ML 239;ML239;1378872-36-6
- CAS:
- 1378872-36-6
- MF:
- C13H10Cl3N3O2
- MW:
- 346.6
- EINECS:
- 604-604-1
- Mol File:
- 1378872-36-6.mol
(2,4,6-Trichloro-phenoxy)-acetic acid (1H-pyrrol-2-ylmethylene)-hydrazide Chemical Properties
- Density
- 1.50±0.1 g/cm3(Predicted)
- storage temp.
- Inert atmosphere,2-8°C
- solubility
- DMSO: soluble15mg/mL (clear solution)
- pka
- 11.95±0.46(Predicted)
- form
- powder
- color
- white to beige
- Stability:
- Stable for 2 years from date of purchase as supplied. Solutions in DMSO, DMF or ethanol may be stored at -20° for up to 3 months.
Safety Information
- Hazard Codes
- Xn
- Risk Statements
- 20/21/22-36/37/38
- Safety Statements
- 26
- RIDADR
- UN 3077 9 / PGIII
- WGK Germany
- 3
(2,4,6-Trichloro-phenoxy)-acetic acid (1H-pyrrol-2-ylmethylene)-hydrazide Usage And Synthesis
Description
ML-
Uses
ML-239, is an inhibitor of breast cancer stem cells, with greater than 23 fold selectivity of inhibition in the cell line.
Definition
ChEBI: N'-(2-pyrrolylidenemethyl)-2-(2,4,6-trichlorophenoxy)acetohydrazide is an aromatic ether.
storage
Store at +4°C
References
[1] LEIGH C. CARMODY . Phenotypic High-Throughput Screening Elucidates Target Pathway in Breast Cancer Stem Cell–Like Cells[J]. SLAS Discovery, 2012, 17 9: Pages 1204-1210. DOI:10.1177/1087057112458317
[2] ANDREW R. GERMAIN . Identification of a selective small molecule inhibitor of breast cancer stem cells[J]. Bioorganic & Medicinal Chemistry Letters, 2012, 22 10: Pages 3571-3574. DOI:10.1016/j.bmcl.2012.01.035
[3] MATTHEW G REES. Correlating chemical sensitivity and basal gene expression reveals mechanism of action[J]. Nature chemical biology, 2015, 12 2: 109-116. DOI:10.1038/nchembio.1986
(2,4,6-Trichloro-phenoxy)-acetic acid (1H-pyrrol-2-ylmethylene)-hydrazideSupplier
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