Basic information Safety Supplier Related

(2,4,6-Trichloro-phenoxy)-acetic acid (1H-pyrrol-2-ylmethylene)-hydrazide

Basic information Safety Supplier Related

(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
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(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.
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Safety Information

Hazard Codes 
Xn
Risk Statements 
20/21/22-36/37/38
Safety Statements 
26
RIDADR 
UN 3077 9 / PGIII
WGK Germany 
3
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(2,4,6-Trichloro-phenoxy)-acetic acid (1H-pyrrol-2-ylmethylene)-hydrazide Usage And Synthesis

Description

ML-239 is an inhibitor of cancer stem cells, displaying greater than 23-fold selective inhibition of a breast cancer stem cell-like cell line (EC50 = 1.18 μM) over an isogenic control cell line (EC50 = 27.6 μM). It is also toxic to the breast carcinoma cell line MDA-MB-231. ML-239 alters the expression of genes in the MAPK, NF-κB, and inflammatory cytokine pathways. It is stable in saline and modestly stable in human plasma.

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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