1. Immunology/Inflammation MAPK/ERK Pathway NF-κB Metabolic Enzyme/Protease Apoptosis
  2. Reactive Oxygen Species Caspase Apoptosis JNK
  3. TASIN-1 hydrochloride

TASIN-1 hydrochloride is a selective inhibitor of truncated APCTR (adenomatous polyposis coli gene) that exerts cytotoxic effects by inhibiting cholesterol biosynthesis. TASIN-1 hydrochloride specifically targets colorectal cancer (CRC) cells carrying APC truncated mutations, while having no significant toxicity to wild-type APC cells. TASIN-1 hydrochloride exerts cytotoxic effects by targeting Emopamil binding protein (EBP) to inhibit cholesterol biosynthesis, triggering endoplasmic reticulum (ER) stress, reactive oxygen species (ROS) generation, and JNK-mediated apoptosis, and inhibiting Akt survival signaling. TASIN-1 hydrochloride can be used to prevent and intervene in APC mutant colorectal cancer.

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

TASIN-1 hydrochloride Chemical Structure

TASIN-1 hydrochloride Chemical Structure

CAS No. : 1678515-13-3

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Description

TASIN-1 hydrochloride is a selective inhibitor of truncated APCTR (adenomatous polyposis coli gene) that exerts cytotoxic effects by inhibiting cholesterol biosynthesis. TASIN-1 hydrochloride specifically targets colorectal cancer (CRC) cells carrying APC truncated mutations, while having no significant toxicity to wild-type APC cells. TASIN-1 hydrochloride exerts cytotoxic effects by targeting Emopamil binding protein (EBP) to inhibit cholesterol biosynthesis, triggering endoplasmic reticulum (ER) stress, reactive oxygen species (ROS) generation, and JNK-mediated apoptosis, and inhibiting Akt survival signaling. TASIN-1 hydrochloride can be used to prevent and intervene in APC mutant colorectal cancer[1][2][3].

IC50 & Target

Caspase 3

 

Caspase-7

 

In Vitro

TASIN-1 hydrochloride selectively inhibits adenomatous polyposis coli truncated (APCTR) in DLD1 cells with IC50=70 nM[1].
TASIN-1 hydrochloride (70 nM; 72 h) significantly inhibits the proliferation of human colon cancer cells DLD1 (APCTR) with IC50 of 70 nM, and has a high selectivity against HCT116 (APCWT) cells with IC50 >50 μM[1].
TASIN-1 hydrochloride (2.5 μM; 7 d) inhibits soft agar colony formation of DLD1 cells, but has no significant effect on HCT116[1].
TASIN-1 hydrochloride (2.5 μM; 2-48 h) reduced the cholesterol synthesis rate and endogenous cholesterol levels in DLD1 cells, but had no effect on HCT116 cells[1].
TASIN-1 hydrochloride (2.5 μM; 24 h) induced the expression of endoplasmic reticulum stress marker CHOP and JNK phosphorylation, and activated caspase 3/7 activity in DLD1 cells, but no significant changes were observed in HCT116 cells[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Viability Assay[1]

Cell Line: DLD1 (APCTR), HCT116 (APCWT)
Concentration: 0.01-100 μM
Incubation Time: 72 h
Result: Showed an IC50 of 70 nM in DLD1 cells and >50 μM in HCT116 cells, demonstrating >700-fold selectivity for APCTR cells.
In Vivo

TASIN-1 (40 mg/kg; ip; twice daily; 18 days) hydrochloride significantly inhibits tumor growth and induced tumor cell apoptosis in the nude mouse DLD1/HT29 (APCTR) subcutaneous xenograft model, without inhibitory effect on HCT116 (APCWT) tumors[1].
TASIN-1 (20, 40 mg/kg; ip; twice weekly; 90 or 100 days) hydrochloride reduces the number and size of colon polyps and inhibits tumor progression in the CPC;Apc mouse genetic colorectal cancer model without significant liver and kidney damage or weight loss[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Female athymic nude mice (5-6 weeks old, ~20 g) with DLD1/HT29 (APCTR) or HCT116 (APCWT) subcutaneous xenograft model[1]
Dosage: 40 mg/kg TASIN-1
Administration: Intraperitoneal (i.p.) injection, twice daily (bid), 18 days
Result: Reduced DLD1 and HT29 tumor volumes by 40%-60% compared to vehicle control, with increased cleaved caspase 3 and PARP in tumor lysates.
Showed no significant growth inhibition against HCT116 tumors.
Tumor histology revealed fragmented nuclei and increased apoptotic cells in treated groups.
Molecular Weight

388.95

Formula

C18H29ClN2O3S

CAS No.
SMILES

CC1CCN(C2CCN(S(=O)(C3=CC=C(OC)C=C3)=O)CC2)CC1.Cl

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Room temperature in continental US; may vary elsewhere.

Storage

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

Purity & Documentation
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    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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TASIN-1 hydrochloride
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HY-116572
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