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Angoline - 99%, high purity , CAS No.21080-31-9

  • ≥99%
Item Number
A649791
Grouped product items
SKUSizeAvailabilityPrice Qty
A649791-5mg
5mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$180.90

Alkaloids Isoquinoline Alkaloids

Basic Description

SynonymsAngoline|21080-31-9|1,2,13-trimethoxy-12-methyl-13H-[1,3]benzodioxolo[5,6-c]phenanthridine|[1,3]Benzodioxolo[5,6-c]phenanthridine, 12,13-dihydro-1,2,13-trimethoxy-12-methyl-|1,2,13-Trimethoxy-12-methyl-12,13-dihydro-[1,3]dioxolo[4',5':4,5]benzo[1,2-c]phen
Specifications & Purity≥99%
Biochemical and Physiological MechanismsAngoline is a potent and selective IL6/STAT3 signaling pathway inhibitor with an IC 50 of 11.56 μM. Angoline inhibits STAT3 phosphorylation and its target gene expression, and inhibits cancer cell proliferation.
Storage TempProtected from light,Store at -80°C
Shipped InIce chest + Ice pads
Product Description

Angoline is a potent and selective IL6/STAT3 signaling pathway inhibitor with an IC 50 of 11.56 μM. Angoline inhibits STAT3 phosphorylation and its target gene expression, and inhibits cancer cell proliferation

In Vitro

Angoline (0-100 μM; 1 h) inhibits STAT3, STAT1 and NF-κB signaling pathways with IC 50 values of 11.56, >100 and >100 μM, respectively. Angoline (0-100 μM; 2 h) affects phosphorylation of STAT3. Angoline (0-100 μM; 72 h) inhibits MDA-MB-231, H4 and HepG2 cells proliferation. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Western Blot AnalysisCell Line: HepG2/STAT3 cell line Concentration: 0, 1, 10, 30 and 100 μM Incubation Time: 2 hours Result: Inhibited IL-6-induced phosphorylation of STAT3 in HepG2/STAT3 cells. Cell Proliferation AssayCell Line: MDA-MB-231, H4 and HepG2 cell lines Concentration: 0-100 μM Incubation Time: 72 hours Result: Inhibited proliferation of MDA-MB-231, H4 and HepG2 cells with IC 50 values of 3.32, 4.72 and 3.14 μM, respectively.

Form:Solid

IC50& Target:IC50: 11.56 μM (IL6/STAT3 signaling pathway), 3.32 μM (MDA-MB-231), 4.72 μM (H4), 3.14 μM (HepG2)

Associated Targets

CYP1A2 Tchem Cytochrome P450 1A2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CYP1B1 Tchem Cytochrome P450 1B1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CYP2D6 Tclin Cytochrome P450 2D6 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CYP2C19 Tchem Cytochrome P450 2C19 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CYP3A4 Tclin Cytochrome P450 3A4 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CYP2C9 Tchem Cytochrome P450 2C9 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CYP1A1 Tchem Cytochrome P450 1A1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name 1,2,13-trimethoxy-12-methyl-13H-[1,3]benzodioxolo[5,6-c]phenanthridine
INCHI InChI=1S/C22H21NO5/c1-23-20-14(6-5-12-9-17-18(10-15(12)20)28-11-27-17)13-7-8-16(24-2)21(25-3)19(13)22(23)26-4/h5-10,22H,11H2,1-4H3
InChi Key LVWAKZBZWYHYCJ-UHFFFAOYSA-N
Canonical SMILES CN1C(C2=C(C=CC(=C2OC)OC)C3=C1C4=CC5=C(C=C4C=C3)OCO5)OC
Isomeric SMILES CN1C(C2=C(C=CC(=C2OC)OC)C3=C1C4=CC5=C(C=C4C=C3)OCO5)OC
Alternate CAS 21080-31-9
PubChem CID 189060
MeSH Entry Terms angoline
Molecular Weight 379.41

Certificates

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Chemical and Physical Properties

SolubilityDMSO : 20.83 mg/mL (54.90 mM; Need ultrasonic)

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Solution Calculators