| Substance | Relationship Strength | Studies | Trials | Classes | Roles |
|---|
guanidine
Guanidine: A strong organic base existing primarily as guanidium ions at physiological pH. It is found in the urine as a normal product of protein metabolism. It is also used in laboratory research as a protein denaturant. (From Martindale, the Extra Pharmacopoeia, 30th ed and Merck Index, 12th ed) It is also used in the treatment of myasthenia and as a fluorescent probe in HPLC.. guanidine : An aminocarboxamidine, the parent compound of the guanidines. | 2.7 | 3 | 0 | carboxamidine;
guanidines;
one-carbon compound | |
isoxazoles
Isoxazoles: Azoles with an OXYGEN and a NITROGEN next to each other at the 1,2 positions, in contrast to OXAZOLES that have nitrogens at the 1,3 positions.. isoxazole : A monocyclic heteroarene with a structure consisting of a 5-membered ring containing three carbon atoms and an oxygen and nitrogen atom adjacent to each other. It is the parent of the class of isoxazoles.. isoxazoles : Oxazoles in which the N and O atoms are adjacent. | 2.41 | 2 | 0 | isoxazoles;
mancude organic heteromonocyclic parent;
monocyclic heteroarene | |
thiazoles
[no description available] | 2.04 | 1 | 0 | 1,3-thiazoles;
mancude organic heteromonocyclic parent;
monocyclic heteroarene | |
arildone
[no description available] | 2.41 | 2 | 0 | methoxybenzenes | |
disoxaril
disoxaril: antipicornavirus agent | 2.41 | 2 | 0 | aromatic ether | |
1-(2',6'-difluorophenyl)-1h,3h-thiazolo(3,4-a)benzimidazole
1-(2',6'-difluorophenyl)-1H,3H-thiazolo(3,4-a)benzimidazole: anti-HIV agent; a non-nucleoside reverse transcriptase inhibitor; structure given in first source | 2.04 | 1 | 0 | | |
ethyl-2-methylthio-4-methyl-5-pyrimidine carboxylate
[no description available] | 2.41 | 2 | 0 | | |
phenylthiourea
Phenylthiourea: Phenylthiourea is a THIOUREA derivative containing a phenyl ring. Depending on their genetic makeup, humans can find it either bitter-tasting or tasteless.. N-phenylthiourea : A member of the class of thioureas that is thiourea in which one of the hydrogens is replaced by a phenyl group. Depending on their genetic makeup, humans find it either very bitter-tasting or tasteless. This unusual property resulted in N-phenylthiourea being used in paternity testing prior to the advent of DNA testing. | 2.41 | 2 | 0 | thioureas | EC 1.14.18.1 (tyrosinase) inhibitor |
n-phenyl-n'-3-hydroxyphenylthiourea
[no description available] | 2.41 | 2 | 0 | | |
viroxime
[no description available] | 2.41 | 2 | 0 | | |