Diethyl Pyrocarbonate|CAS 1609-47-8|DC Chemicals

Cas No.:	1609-47-8
Chemical Name:	Diethyl pyrocarbonate
Synonyms:	Diethyl pyrocarbonate;Diethyl oxydiformate;Ethoxyformic anhydride;Pyrocarbonic acid diethyl ester;Diethyl dicarbonate;dicarbonicaciddiethylester;Diethyl ester of pyrocarbonic acid;Diethyl pyrocarbonic acid;Diethylester kyseliny diuhlicite;DEPC;DIETHYLPYROCARBONATE (DEPC);DEP,DEPC,Diethyl dicarbonate;ethoxycarbonyl ethyl carbonate;Ethoxyformic acid anhydride;DEP;Baycovin;Ethyl pyrocarbonate;Diethylpyrocarbonate;Dicarbonic acid, diethyl ester;Dicarbonic acid diethyl ester;Piref;Diethylpyrokarbonat;Oxydiformic acid diethyl ester;Pyrocarbonate d'ethyle;Pyrokohlensaeure diaethyl ester;Pyrocarbonic acid, diethyl ester
SMILES:	O(C(=O)OC(=O)OC([H])([H])C([H])([H])[H])C([H])([H])C([H])([H])[H]
Formula:	C₆H₁₀O₅
M.Wt:	162.1406
Purity:	>98%
Sotrage:	2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO

Description:	Diethyl pyrocarbonate is a potent, non-specific inhibitor of RNase. It has been useful as an in vitro agent, relatively specific for binding to imidazole of histidine. It inhibits central chemosensitivity in rabbit and can modify Ser, Thr, His and Tyr residues.
References:	[1]. E E Nattie. Diethyl pyrocarbonate (an imidazole binding substance) inhibits rostral VLM CO2 sensitivity. J Appl Physiol (1985). 1986 Sep;61(3):843-50.

MSDS

Cat. No.	Product name	Field of application
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DC73194	Fraisinib	Fraisinib is a specific and effective inhibitor of glycyl-tRNA synthetase 1 (GARS1), suppresses the synthesis of Ap4A by GARS1 and displays strong anti-tumoral potential.
DC72861	Diethyl Pyrocarbonate	Diethyl pyrocarbonate is a potent, non-specific inhibitor of RNase. It has been useful as an in vitro agent, relatively specific for binding to imidazole of histidine. It inhibits central chemosensitivity in rabbit and can modify Ser, Thr, His and Tyr residues.
DC72313	Dideoxy-amanitin	Dideoxy-amanitin (compound 2), an α-Amanitin derivative, is a potent and selective RNA polymerase II allosteric inhibitor with an IC50 value of 74.2 nM.
DC72169	RP-6685	RP-6685 is a potent, selective and orally active DNA polymerase theta (Polθ) inhibitor with an IC50 value of 5.8 nM (PicoGreen assay). RP-6685 shows antitumor efficacy in mouse tumor xenograft model.
DC71300	Branaplam hydrochloride	Branaplam (LMI070; NVS-SM1) hydrochloride is a highly potent, selective and orally active survival motor neuron-2 (SMN2) splicing modulator with an EC50 of 20 nM for SMN. Branaplam hydrochloride inhibits human-ether-a-go-go-related gene (hERG) with an IC50 of 6.3 μM. Branaplam hydrochloride elevates full-length SMN protein and extends survival in a severe spinal muscular atrophy (SMA) mouse model.
DC45555	SCR130	SCR130 is a novel DNA repair inhibitor with IC50s of 14 μM in Reh cells and 2 μM in Nalm6 cells. SCR130 specifically inhibits DNA Ligase IV‐mediated joining with minimal or no effect on Ligase III and Ligase I mediated joining.
DC45554	Aplidine	Aplidine (Plitidepsin) is a potent anti-cancer agent by targeting eEF1A2 ( KD=80 nM). Aplidine possesses antiviral activity and is against SARS-CoV-2 with an IC90 of 0.88 nM. Aplidine is usually used for multiple myeloma and advanced cancer research, and has the potential for COVID-19 research.
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