S-(2-Aminoethyl)pseudothiourea dihydrobromide
S-(2-Aminoethyl)pseudothiourea dihydrobromide structure
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Common Name | S-(2-Aminoethyl)pseudothiourea dihydrobromide | ||
|---|---|---|---|---|
| CAS Number | 56-10-0 | Molecular Weight | 281.013 | |
| Density | N/A | Boiling Point | 231.1ºC at 760mmHg | |
| Molecular Formula | C3H11Br2N3S | Melting Point | 190-196 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 93.6ºC | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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Chemical genetics reveals a complex functional ground state of neural stem cells.
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Differential activity of NO synthase inhibitors as chemopreventive agents in a primary rat tracheal epithelial cell transformation system.
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Certain S-substituted isothioureas not only inhibit NO synthase catalytic activity but also decrease translation and stability of inducible NO synthase protein.
Nitric Oxide 2(3) , 155-64, (1998) In an attempt to identify potent inhibitors of inducible (type II) NO synthase (iNOS) for use in cell culture systems, we found that two S-substituted isothioureas were very potent in cell culture but one such compound also interfered with the induction of NO... |
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Pathophysiological role of nitric oxide in rat experimental colitis.
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Selective inhibition of inducible nitric oxide synthase maintains haemodynamic stability without untoward consequences for hepatic function or morphology.
Eur. J. Surg. 165(12) , 1167-74, (1999) To examine the effects of the inducible nitric oxide synthase inhibitor aminoethyl-isothiourea (AE-ITU) on haemodynamic measurements, and correlate these with hepatic morphology and function in a porcine model of endotoxaemia.Experimental study.15 juvenile pi... |