000			01389 a2200409 4500
005			20250513113745.0
264		0	_c19970501
008			199705s 0 0 eng d
022			_a0022-2623
024	7		_a10.1021/jm960762y _2doi
040			_aNLM _beng _cNLM
100	1		_aTucker, T J
245	0	0	_aDesign of highly potent noncovalent thrombin inhibitors that utilize a novel lipophilic binding pocket in the thrombin active site. _h[electronic resource]
260			_bJournal of medicinal chemistry _cMar 1997
300			_a830-2 p. _bdigital
500			_aPublication Type: Journal Article
650	0	4	_aBinding Sites
650	0	4	_aCrystallography, X-Ray
650	0	4	_aCyclohexylamines _xchemical synthesis
650	0	4	_aDipeptides _xchemical synthesis
650	0	4	_aDrug Design
650	0	4	_aFibrinolytic Agents _xchemical synthesis
650	0	4	_aHydrogen Bonding
650	0	4	_aMolecular Structure
650	0	4	_aProtein Binding
650	0	4	_aThrombin _xantagonists & inhibitors
700	1		_aLumma, W C
700	1		_aMulichak, A M
700	1		_aChen, Z
700	1		_aNaylor-Olsen, A M
700	1		_aLewis, S D
700	1		_aLucas, R
700	1		_aFreidinger, R M
700	1		_aKuo, L C
773	0		_tJournal of medicinal chemistry _gvol. 40 _gno. 6 _gp. 830-2
856	4	0	_uhttps://doi.org/10.1021/jm960762y _zAvailable from publisher's website
999			_c9068073 _d9068073