Tetrazanbigen

SKU:BHB21902448
Overview
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Tetrazanbigen (CAS 2121990-04-1) is a bioactive small molecule. Relevant to Apoptosis research. Molecular formula C18H16N4, molecular weight 288.35 g/mol. Also known as TNBG.
CAS Number 2121990-04-1
Molecular Weight 288.35 g/mol
Storage See Certificate of Analysis
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Catalog no. Size
HY-176249-50MG 50 mg
HY-176249-100MG 100 mg
HY-176249-250MG 250 mg
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Field Specification
Alternative names TNBG
CAS no. 2121990-04-1
Applications
  • Functional Assay (In Vitro)
Molecular weight 288.35
Molecular formula C18H16N4
SMILES C1(N=C2N3CCC4=C(C=CC=C4)C3CN=C2N5)=C5C=CC=C1
Storage Refer to Certificate of Analysis (CoA) for storage conditions
Shipping Room temperature in continental US; may vary elsewhere.
Catalog no. (Mfr.) HY-176249
Main SKU BHB21902448
Bioactive Small Molecules

Compound Overview

Tetrazanbigen, also known as TNBG, is a potent, selective antitumor agent that shows strong antitumor efficacy against six human cancer cell lines, with an IC50 range of 2.13-8.01 μg/mL, and an IC50 of 11.25 μg/mL against normal hepatocytes. It induces S phase arrest and apoptosis in QGY-7701 cells, and it exerts its antitumor activity by inducing lipid accumulation in cancer cells[1]. It has the molecular formula C18H16N4 and a molecular weight of 288.35 g/mol.

Physical & Chemical Properties

CAS Number 2121990-04-1
Molecular Formula C18H16N4
Molecular Weight 288.35 g/mol
SMILES C1(N=C2N3CCC4=C(C=CC=C4)C3CN=C2N5)=C5C=CC=C1
Signaling Pathway Apoptosis
Storage Please store the product under the recommended conditions in the Certificate of Analysis.
Shipping Room temperature in continental US; may vary elsewhere.

Literature Cited

Sources cited in this description and in the In Vitro & In Vivo Data tab. Peer-reviewed publications that used this product are listed under References.

[1]. Zheng X, et al. Antitumour effects of tetrazanbigen against human hepatocellular carcinoma QGY-7701 through inducing lipid accumulation in vitro and in vivo. J Pharm Pharmacol. 2015 Nov;67(11):1593-602.

Safety

For Research Use Only. Not for use in diagnostic or therapeutic procedures, and not for human or veterinary use. Handle in accordance with your institution's chemical hygiene plan.

In Vitro

Tetrazanbigen (0-12 μg/mL, 72 h) reduces the proliferation of QGY-7701, BIU-87, Hep-2, SGC-7901, K562, SW626, and LO2 cells, giving IC50 values (in that order) of 2.13, 3.25, 3.84, 4.41, 7.70, 8.01, and 11.25 μg/mL[1].

Lipid accumulation is induced in QGY-7701 cells by Tetrazanbigen (0-8 μg/mL, 24-72 h)[1].

Tetrazanbigen (2-4 μg/mL, 72 h) causes S phase cell cycle arrest and apoptosis in QGY-7701 cells[1].

Cell Cycle Analysis[1]

Cell LineQGY-7701 cells
Concentration2 μg/mL, 4 μg/mL
Incubation Time72 h
ResultIncreased the population of S phase, decreased the populations of G0/G1 phases.

Apoptosis Analysis[1]

Cell LineQGY-7701 cells
Concentration4 μg/mL
Incubation Time72 h
ResultInduced apoptosis, and caused condensed nuclei, apoptotic bodies and cellular shrinkage, chromatin margination. Caused the appearance of a large number of lipid droplets.

In Vivo

In nude mice, Tetrazanbigen (1.5 mg/kg/day, i.p., 5 weeks) suppresses tumor growth and shows good safety[1].

Animal ModelNude mice (Female athymic of 4 weeks old) bearing xenografts of QGY-7701 cell line (5 × 106, s.c.) [1]
Dosage1.5 mg/kg/day
Administrationi.p., 5 weeks
ResultReduced tumor volume and inhibited tumor weight, the TGI based on tumor weight was 87%.

Data provided by the manufacturer. Numbered citations refer to the Literature Cited list in the product description.

Q.Why is there no price listed?
A.Every size of this product is quoted on inquiry. Send us the size you need and we will come back with price and lead time.
Q.Can this be used in humans or for diagnostics?
A.No. This product is supplied For Research Use Only. It is not for diagnostic or therapeutic procedures and not for human or veterinary use.

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