![]() Triphenylmethanamine structure
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Common Name | Triphenylmethanamine | ||
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CAS Number | 5824-40-8 | Molecular Weight | 259.345 | |
Density | 1.1±0.1 g/cm3 | Boiling Point | 369.3±0.0 °C at 760 mmHg | |
Molecular Formula | C19H17N | Melting Point | 102-104 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 190.9±12.3 °C | |
Symbol |
![]() GHS07 |
Signal Word | Warning |
Structure-activity relationship of S-trityl-L-cysteine analogues as inhibitors of the human mitotic kinesin Eg5.
J. Med. Chem. 51 , 1115-25, (2008) The human kinesin Eg5 is a potential drug target for cancer chemotherapy. Eg5 specific inhibitors cause cells to block in mitosis with a characteristic monoastral spindle phenotype. Prolonged metaphase block eventually leads to apoptotic cell death. S-trityl-... |
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Triarylmethanes, a new class of cx50 inhibitors.
Front. Pharmacol. 3 , 106, (2012) The paucity of specific pharmacological agents has been a major impediment for delineating the roles of gap junction (GJ) channels formed by connexin proteins in physiology and pathophysiology. Here, we used the selective optimization of side activities (SOSA... |
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Novel inhibitors of the Gardos channel for the treatment of sickle cell disease.
J. Med. Chem. 51 , 976-82, (2008) Sickle cell disease (SCD) is a hereditary condition characterized by deformation of red blood cells (RBCs). This phenomenon is due to the presence of abnormal hemoglobin that polymerizes upon deoxygenation. This effect is exacerbated when dehydrated RBCs expe... |
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Reaction of triphenylmethylamines with boron trihalides. Ronan RJ, et al.
J. Am. Chem. Soc. 93(25) , 6811-14, (1971)
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Tritylamine (triphenylmethylamine) in organic synthesis; II. The reaction of tritylamine with oxiranes-synthesis of N-trityl-ß aminoalcohols. Soroka M and Goldeman W.
ARKIVOC 12 , 31-37, (2003)
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Role-allocated combination of two types of hydrogen bonds towards constructing a breathing diamondoid porous organic salt.
Chemistry 19(9) , 3006-16, (2013) A diamondoid porous organic salt (d-POS) composed of 8-hydroxyquinoline-5-sulfonic acid (HQS) and triphenylmethylamine (TPMA) shows reversible structure contraction and expansion ("breathing") in response to guest desorption and adsorption. This flexible stru... |
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