Anticancer agent 137

Cat. No.: HY-155570: Data Sheet Handling Instructions
FAQs
Technical Support

Anticancer agent 137 (8q) is a potent PI3k inhibitor. Anticancer agent 137 has broad-spectrum anticancer activity. Anticancer agent 137 induces G2/M cell cycle arrest and apoptosis. Anticancer agent 137 increases cleaved PARP, caspase 3, and 7. Anticancer agent 137 can be used in research of cancer.

For research use only. We do not sell to patients.

Anticancer agent 137 Chemical Structure

Size		Stock
MOQ		Minimum order quantity
50 mg		Get quote
100 mg		Get quote
250 mg		Get quote
Other size		Get quote

* Please select Quantity before adding items.

This product is a controlled substance and not for sale in your territory.

Featured Recommendations

•Related Small Molecules:

•Related Proteins:

View All PI3K Isoform Specific Products:

View All Isoforms

PI3Kα PI3Kβ PI3Kγ PI3Kδ PI3KC2α PI3KC2β PI3KC2γ Vps34 PI3K PI3KC3 p120γ

View All Caspase Isoform Specific Products:

View All Isoforms

Caspase 1 Caspase 2 Caspase 3 Caspase 4 Caspase 5 Caspase 6 Caspase 7 Caspase 8 Caspase 9 Caspase 10 Caspase 12 Caspase Caspase 11 Caspase-13

View All PARP Isoform Specific Products:

View All Isoforms

PARP PARP1 PARP2 PARP3 PARP4 TNKS1/PARP5A TNKS2/PARP5B PARP7 PARP10 PARP14 PARP15 PARP12 PARP16

Biological Activity
Purity & Documentation
References
Customer Review

Description

Cellular Effect

Cell Line	Type	Value	Description	References
A498	GI₅₀	1.38 μM Compound: 8q	Growth inhibition of human A498 cells measured after 24 to 72 hrs by SRB method Growth inhibition of human A498 cells measured after 24 to 72 hrs by SRB method	[PMID: 37163949]
ACHN	GI₅₀	4.27 μM Compound: 8q	Growth inhibition of human ACHN cells measured after 24 to 72 hrs by SRB method Growth inhibition of human ACHN cells measured after 24 to 72 hrs by SRB method	[PMID: 37163949]
COLO 205	GI₅₀	2.4 μM Compound: 8q	Growth inhibition of human COLO 205 cells measured after 24 to 72 hrs by SRB method Growth inhibition of human COLO 205 cells measured after 24 to 72 hrs by SRB method	[PMID: 37163949]
DU-145	GI₅₀	2.95 μM Compound: 8q	Growth inhibition of human DU-145 cells measured after 24 to 72 hrs by SRB method Growth inhibition of human DU-145 cells measured after 24 to 72 hrs by SRB method	[PMID: 37163949]
IGROV-1	GI₅₀	2.82 μM Compound: 8q	Growth inhibition of human IGROV-1 cells measured after 24 to 72 hrs by SRB method Growth inhibition of human IGROV-1 cells measured after 24 to 72 hrs by SRB method	[PMID: 37163949]
KM12	GI₅₀	3.47 μM Compound: 8q	Growth inhibition of human KM12 cells measured after 24 to 72 hrs by SRB method Growth inhibition of human KM12 cells measured after 24 to 72 hrs by SRB method	[PMID: 37163949]
MDA-MB-435	GI₅₀	0.52 μM Compound: 8q	Growth inhibition of human MDA-MB-435 cells measured after 24 to 72 hrs by SRB method Growth inhibition of human MDA-MB-435 cells measured after 24 to 72 hrs by SRB method	[PMID: 37163949]
NCI/ADR-RES	GI₅₀	2.82 μM Compound: 8q	Growth inhibition of human NCI-ADR-RES cells measured after 24 to 72 hrs by SRB method Growth inhibition of human NCI-ADR-RES cells measured after 24 to 72 hrs by SRB method	[PMID: 37163949]
OVCAR-3	GI₅₀	2.82 μM Compound: 8q	Growth inhibition of human OVCAR-3 cells measured after 24 to 72 hrs by SRB method Growth inhibition of human OVCAR-3 cells measured after 24 to 72 hrs by SRB method	[PMID: 37163949]
OVCAR-4	GI₅₀	2.82 μM Compound: 8q	Growth inhibition of human OVCAR-4 cells measured after 24 to 72 hrs by SRB method Growth inhibition of human OVCAR-4 cells measured after 24 to 72 hrs by SRB method	[PMID: 37163949]
OVCAR-5	GI₅₀	2.82 μM Compound: 8q	Growth inhibition of human OVCAR-5 cells measured after 24 to 72 hrs by SRB method Growth inhibition of human OVCAR-5 cells measured after 24 to 72 hrs by SRB method	[PMID: 37163949]
OVCAR-8	GI₅₀	2.82 μM Compound: 8q	Growth inhibition of human OVCAR-8 cells measured after 24 to 72 hrs by SRB method Growth inhibition of human OVCAR-8 cells measured after 24 to 72 hrs by SRB method	[PMID: 37163949]
PC-3	GI₅₀	1.58 μM Compound: 8q	Growth inhibition of human PC-3 cells measured after 24 to 72 hrs by SRB method Growth inhibition of human PC-3 cells measured after 24 to 72 hrs by SRB method	[PMID: 37163949]
SF-268	GI₅₀	5.13 μM Compound: 8q	Growth inhibition of human SF-268 cells measured after 24 to 72 hrs by SRB method Growth inhibition of human SF-268 cells measured after 24 to 72 hrs by SRB method	[PMID: 37163949]
SF-295	GI₅₀	2.51 μM Compound: 8q	Growth inhibition of human SF-295 cells measured after 24 to 72 hrs by SRB method Growth inhibition of human SF-295 cells measured after 24 to 72 hrs by SRB method	[PMID: 37163949]
SK-MEL-28	GI₅₀	4.07 μM Compound: 8q	Growth inhibition of human SK-MEL-28 cells measured after 24 to 72 hrs by SRB method Growth inhibition of human SK-MEL-28 cells measured after 24 to 72 hrs by SRB method	[PMID: 37163949]
SK-OV-3	GI₅₀	2.82 μM Compound: 8q	Growth inhibition of human SK-OV-3 cells measured after 24 to 72 hrs by SRB method Growth inhibition of human SK-OV-3 cells measured after 24 to 72 hrs by SRB method	[PMID: 37163949]

Molecular Weight

449.50

Formula

C₂₆H₂₇NO₆

SMILES

COC1=C(C(OC)=CC2=C1CCC(O2)C3=CC=CC(C(NC4=CC=C(C=C4)OC)=O)=C3)OC

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation

Handling Instructions (2659 KB)

References

[1]. Hassan AHE, et, al. Scaffold hopping of N-benzyl-3,4,5-trimethoxyaniline: 5,6,7-Trimethoxyflavan derivatives as novel potential anticancer agents modulating hippo signaling pathway. Eur J Med Chem. 2023 Aug 5;256:115421. [Content Brief]