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Valrubicin

Catalog No. T7604 CAS 56124-62-0

Synonyms: Valstar, AD-32

Valrubicin (AD-32) (AD 32) inhibits TPA- and PDBu-induced PKC activation (IC50s: 0.85 and 1.25 μM) and has antitumor and anti-inflammatory activity.

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Valrubicin, CAS 56124-62-0

Pack Size	Availability	Price/USD
1 mg	In stock	$ 64.00
5 mg	In stock	$ 155.00
10 mg	In stock	$ 229.00
25 mg	In stock	$ 388.00
50 mg	In stock	$ 566.00
100 mg	In stock	$ 790.00

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Purity: 97.41%

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Description	Valrubicin (AD-32) (AD 32) inhibits TPA- and PDBu-induced PKC activation (IC50s: 0.85 and 1.25 μM) and has antitumor and anti-inflammatory activity.
Targets&IC50	PKC (TPA-activated):0.85 μM, PKC (PDBu-induced):1.25 μM
In vitro	Valrubicin inhibits the binding of [3H]PDBu to PKC. Therefore, Valrubicin competes with the tumor promoter for the PKC binding site and prevents the latter from both interacting with the phospholipid and binding to PKC [1]. Valrubicin shows cytotoxic activity against squamous cell carcinoma (SCC) cell line colony formation, with IC50s and IC90s of 8.24 μM and 14.81 μM for UMSCC5 cells, 15.90 μM, 29.84 μM for UMSCC5/CDDP? cells, and 10.50 μM, 19.00 μM for UMSCC10b cells, respectively [2].
In vivo	Valrubicin, administered at doses of 3, 6, or 9 mg, effectively reduces tumor growth through intratumoral injections in hamsters by the third week. When 6 mg of Valrubicin is used in conjunction with minimally cytotoxic irradiation (ranging from 150, 250, or 350 cGy), it induces significant tumor shrinkage in the hamster model [2]. Additionally, at a concentration of 0.1 μg/μL, Valrubicin markedly decreases the infiltration of neutrophils in TPA-challenged biopsies at 24 hours and mitigates chronic inflammation in mice. Furthermore, Valrubicin reduces the expression of inflammatory cytokines in the acute experimental setup [3].
Cell Research	UMSCC5 cells exposed to Valrubicin (2 μM for 3 h), a single dose of radiation (400 cGy), or the combined treatment are cultured for a further 12, 24, or 48 hours. At these times, the cells are collected by trypsinization (0.25%), washed in PBS, and fixed at 5 × 10^6 cells/mL with 95% ethanol. Cells are incubated with ribonuclease (50 μg; 70-90 Kunitz units/mg for 30 min), and the resulting pellet resuspended in and incubated with propidium iodide (0.05 mg/mL for 10 min). The DNA content of the samples is determined by flow cytometry according to standard technique [2].
Animal Research	Hamsters with cheek pouch tumors of 100 mm2 are randomly assigned to one of five treatment groups. Momentarily anesthetized animals each receives once a week × 3 injections (27 g × 0.5-inch needle: 0.1 mL administered slowly to the base of the lesion) of Valrubicin (3, 6, or 9 mg) or drug vehicle (Cremophor: alcohol;1:1 by volume; NaCl diluent 12). A further group of animals receives anesthesia but no direct tumor treatment (control). Individual tumor sizes are measured with calipers at weekly intervals for 4 weeks, at which time the animals are sacrificed [2].

Synonyms	Valstar, AD-32
Molecular Weight	723.64
Formula	C34H36F3NO13
CAS No.	56124-62-0

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

DMSO: 125 mg/mL (172.74 mM)

H2O: Insoluble

References and Literature

1. Chuang LF, et al. Activation of human leukemia protein kinase C by tumor promoters and its inhibition by N-trifluoroacetyladriamycin-14-valerate (AD 32). Biochem Pharmacol. 1992 Feb 18;43(4):865-72. 2. Wani MK, et al. Rationale for intralesional valrubicin in chemoradiation of squamous cell carcinoma of the head and neck. Laryngoscope. 2000 Dec;110(12):2026-32. 3. Hauge E, et al. Topical valrubicin application reduces skin inflammation in murine models. Br J Dermatol. 2012 Aug;167(2):288-95.

Related compound libraries

This product is contained In the following compound libraries：

Anti-Cancer Approved Drug Library Inhibitor Library Anti-Cancer Clinical Compound Library FDA-Approved Kinase Inhibitor Library Kinase Inhibitor Library Anti-Cancer Active Compound Library Anti-Cancer Drug Library Drug Repurposing Compound Library TGF-beta/Smad Compound Library FDA-Approved & Pharmacopeia Drug Library

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Keywords

Valrubicin 56124-62-0 Chromatin/Epigenetic Cytoskeletal Signaling Microbiology/Virology Antibiotic PKC Inhibitor Valstar inhibit AD-32 AD 32 Protein kinase C AD32 inhibitor

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