FIDAS-3 - 99%, high purity , CAS No.1266684-01-8

  • ≥99%
Item Number
F648665
Grouped product items
SKUSizeAvailabilityPrice Qty
F648665-1mg
1mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$71.90
F648665-5mg
5mg
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Production requires sourcing of materials. We appreciate your patience and understanding.
$150.90
F648665-10mg
10mg
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$240.90
F648665-25mg
25mg
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$460.90
F648665-50mg
50mg
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$750.90
F648665-100mg
100mg
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$1,190.90
View related series
Stem Cell/Wnt Wnt

Basic Description

Specifications & Purity≥99%
Biochemical and Physiological MechanismsFIDAS-3 is a stilbene derivative and is a potent Wnt inhibitor with an IC 50 of 4.9 μM for methionine S-adenosyltransferase 2A (MAT2A) . FIDAS-3 effectively competes against S-adenosylmethionine (SAM) for MAT2A binding. FIDAS-3 has anticancer activities [
Storage TempProtected from light,Store at -80°C
Shipped InIce chest + Ice pads
Product Description

FIDAS-3 is a stilbene derivative and is a potent Wnt inhibitor with an IC 50 of 4.9 μM for methionine S-adenosyltransferase 2A (MAT2A) . FIDAS-3 effectively competes against S-adenosylmethionine (SAM) for MAT2A binding. FIDAS-3 has anticancer activities

In Vitro

FIDAS-3 (3 μM; 7 days; LS174T cells) treatment significantly inhibits the proliferation of LS174T cells. FIDAS-3 (3-10 μM) treatment inhibits the expression of c-Myc and cyclinD1 in LS174T CRC cells. And FIDAS-3 induces the expression of cell cycle inhibitor, p21 WAF1/CIP1. FIDAS-3 (10 μM; 36 h) treatment reduces the levels of both S-adenosylmethionine (SAM) and S-adenosylhomocysteine (SAH) in LS174T cells. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Cell Viability AssayCell Line: LS174T colorectal cancer (CRC) cells Concentration: 3 μM Incubation Time: 7 days Result: Significantly inhibited the proliferation of LS174T cells.

In Vivo

FIDAS-3 (20 mg/kg; intraperitoneal injection; daily; for one months; C57BL/6J athymic nude mice) treatment significantly inhibits the growth of xenograft tumors. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: C57BL/6J athymic nude mice (6-8 week) injected with LS174 cellsDosage: 20 mg/kg Administration: Intraperitoneal injection; daily; for one months Result: Significantly inhibited the growth of xenograft tumors.

Form:Solid

IC50& Target:IC50: 4.9 μM (Methionine S-adenosyltransferase 2A (MAT2A))

Associated Targets(Human)

KCNH2 Tclin HERG (29587 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
LS174T (446 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MAT2A Tchem S-adenosylmethionine synthase isoform type-2 (713 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Mus musculus (284745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Names and Identifiers

IUPAC Name 4-[(E)-2-(2,6-difluorophenyl)ethenyl]-N,N-dimethylaniline
INCHI InChI=1S/C16H15F2N/c1-19(2)13-9-6-12(7-10-13)8-11-14-15(17)4-3-5-16(14)18/h3-11H,1-2H3/b11-8+
InChi Key YBJDCOLXJYDHOM-DHZHZOJOSA-N
Canonical SMILES CN(C)C1=CC=C(C=C1)C=CC2=C(C=CC=C2F)F
Isomeric SMILES CN(C)C1=CC=C(C=C1)/C=C/C2=C(C=CC=C2F)F
PubChem CID 51039205
Molecular Weight 259.29

Certificates

Certificate of Analysis(COA)

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Chemical and Physical Properties

SolubilityDMSO : 100 mg/mL (385.67 mM; Need ultrasonic)

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