| Weight | 127.187 g/mol |
|---|---|
| Formula | C7H13NO |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
CYCLOHEXANECARBOXAMIDE (1122-56-1)
carboxide · dihexamethylenecarbamide · cyclohexamethylene carbamide
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- 5-Hydroxytryptamine1A Receptor Occupancy by Novel Full Antagonist 2-[4-[4-(7-Chloro-2,3-dihydro-1,4-benzdioxyn-5-yl)-1-piperazinyl]butyl]-1,2-benzisothiazol-3-(2H)-one-1,1-dioxide: A [11C][O-methyl-3H]-N-(2-(4-(2-methoxyphenyl)-1-piperazinyl)ethyl)-N-(2-pyridinyl)cyclohexanecarboxamide Trihydrochloride (WAY-100635) Positron Emission Tomography Study in Humans (Journal of Pharmacology and Experimental Therapeutics, 2002)
- Silicon carboxide ceramics from spirosiloxanes (1992)
- Beta-substituted cyclohexanecarboxamide: a nonpeptidic framework for the design of potent inhibitors of cathepsin K. (Journal of Medicinal Chemistry, 2006)
- Synthesis and characterization of N -(alky(aryl)carbamothioyl)cyclohexanecarboxamide derivatives and their Ni(II) and Cu(II) complexes (Journal of Coordination Chemistry, 2009)
- Synthesis and characterization of N-(Arylcarbamothioyl)-cyclohexanecarboxamide derivatives: the crystal structure of N-(naphthalen-1-ylcarbamothioyl)cyclohexanecarboxamide. (Molecules, 2009)
- (1R,2R)-N-(1-cyanocyclopropyl)-2-(6-methoxy-1,3,4,5-tetrahydropyrido[4,3-b]indole-2-carbonyl)cyclohexanecarboxamide (AZD4996): a potent and highly selective cathepsin K inhibitor for the treatment of osteoarthritis. (Journal of Medicinal Chemistry, 2012)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - carboxide
- dihexamethylenecarbamide
- cyclohexamethylene carbamide
-
SMILESC1CCC(CC1)C(=O)N
-
InChIKeyPNZXMIKHJXIPEK-UHFFFAOYSA-N
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CYCLOHEXANECARBOXAMIDE
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