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Cyclic Nucleotide -- See Nucleotides, Cyclic


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Cyclic Olefins -- See Cycloparaffins


Alicyclic hydrocarbons in which three or more of the carbon atoms in each molecule are united in a ring structure and each of the ring carbon atoms is joined to two hydrogen atoms or alkyl groups. The simplest members are cyclopropane (C3H6), cyclobutane (C4H8), cyclohexane (C6H12), and derivatives of these such as methylcyclohexane (C6H11CH3). (From Sax, et al., Hawley's Condensed Chemical Dictionary, 11th ed)
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Cyclic Somatostatin -- See Somatostatin


A 14-amino acid peptide named for its ability to inhibit pituitary GROWTH HORMONE release, also called somatotropin release-inhibiting factor. It is expressed in the central and peripheral nervous systems, the gut, and other organs. SRIF can also inhibit the release of THYROID-STIMULATING HORMONE; PROLACTIN; INSULIN; and GLUCAGON besides acting as a neurotransmitter and neuromodulator. In a number of species including humans, there is an additional form of somatostatin, SRIF-28 with a 14-amino acid extension at the N-terminal.
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Cyclicity -- See Periodicity


The tendency of a phenomenon to recur at regular intervals; in biological systems, the recurrence of certain activities (including hormonal, cellular, neural) may be annual, seasonal, monthly, daily, or more frequently (ultradian).
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Your entry Cyclin D1 would be here
 

Cyclin-Dependent Kinase -- See Cyclin-Dependent Kinases


Protein kinases that control cell cycle progression in all eukaryotes and require physical association with CYCLINS to achieve full enzymatic activity. Cyclin-dependent kinases are regulated by phosphorylation and dephosphorylation events.
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Cyclin-Dependent Kinases.   3
Cyclin-Dependent Kinases -- antagonists & inhibitors.   2
Cyclin-Dependent Kinases -- therapeutic use.   2
 

Cyclin-Dependent Protein Kinase -- See Cyclin-Dependent Kinases


Protein kinases that control cell cycle progression in all eukaryotes and require physical association with CYCLINS to achieve full enzymatic activity. Cyclin-dependent kinases are regulated by phosphorylation and dephosphorylation events.
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Cyclization.   2001 1
 

Cyclo-Oxygenase Inhibitor -- See Cyclooxygenase Inhibitors


Compounds or agents that combine with cyclooxygenase (PROSTAGLANDIN-ENDOPEROXIDE SYNTHASES) and thereby prevent its substrate-enzyme combination with arachidonic acid and the formation of eicosanoids, prostaglandins, and thromboxanes.
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Cycloaddition -- See Cycloaddition Reaction


Synthetic organic reactions that use reactions between unsaturated molecules to form cyclical products.
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Cycloaddition Reaction.   2009 1
 

Cycloalkanes -- See Cycloparaffins


Alicyclic hydrocarbons in which three or more of the carbon atoms in each molecule are united in a ring structure and each of the ring carbon atoms is joined to two hydrogen atoms or alkyl groups. The simplest members are cyclopropane (C3H6), cyclobutane (C4H8), cyclohexane (C6H12), and derivatives of these such as methylcyclohexane (C6H11CH3). (From Sax, et al., Hawley's Condensed Chemical Dictionary, 11th ed)
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Cycloalkenes -- See Cycloparaffins


Alicyclic hydrocarbons in which three or more of the carbon atoms in each molecule are united in a ring structure and each of the ring carbon atoms is joined to two hydrogen atoms or alkyl groups. The simplest members are cyclopropane (C3H6), cyclobutane (C4H8), cyclohexane (C6H12), and derivatives of these such as methylcyclohexane (C6H11CH3). (From Sax, et al., Hawley's Condensed Chemical Dictionary, 11th ed)
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Cycloalkynes -- See Cycloparaffins


Alicyclic hydrocarbons in which three or more of the carbon atoms in each molecule are united in a ring structure and each of the ring carbon atoms is joined to two hydrogen atoms or alkyl groups. The simplest members are cyclopropane (C3H6), cyclobutane (C4H8), cyclohexane (C6H12), and derivatives of these such as methylcyclohexane (C6H11CH3). (From Sax, et al., Hawley's Condensed Chemical Dictionary, 11th ed)
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Cycloamylose -- See Cyclodextrins


A homologous group of cyclic GLUCANS consisting of alpha-1,4 bound glucose units obtained by the action of cyclodextrin glucanotransferase on starch or similar substrates. The enzyme is produced by certain species of Bacillus. Cyclodextrins form inclusion complexes with a wide variety of substances.
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Cyclodextrin -- See Cyclodextrins


A homologous group of cyclic GLUCANS consisting of alpha-1,4 bound glucose units obtained by the action of cyclodextrin glucanotransferase on starch or similar substrates. The enzyme is produced by certain species of Bacillus. Cyclodextrins form inclusion complexes with a wide variety of substances.
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Cyclodextrins.   2
Cyclodextrins -- analysis.   3
Cyclodextrins -- chemistry.   3
Cyclodextrins -- isolation & purification.   1990 1
Cyclodextrins -- pharmacology.   1999 1
Cyclodextrins -- therapeutic use.   1999 1
Cyclohexane.   2002 1
Cyclohexanes -- metabolism.   1970 1
Cyclohexanes -- toxicity.   1986 1
Cyclohexenes -- chemistry.   2005 1
 

Cyclone -- See Cyclonic Storms


Non-frontal low-pressure systems over tropical or sub-tropical waters with organized convection and definite pattern of surface wind circulation.
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Cyclones -- See Cyclonic Storms


Non-frontal low-pressure systems over tropical or sub-tropical waters with organized convection and definite pattern of surface wind circulation.
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Cyclonic Storms.   11
Cyclonic Storms -- history -- Louisiana -- New Orleans.   2013 1
Cyclooxygenase 1.   2010 1
 

Cyclooxygenase 1 antagonists & inhibitors -- See Cyclooxygenase Inhibitors


Compounds or agents that combine with cyclooxygenase (PROSTAGLANDIN-ENDOPEROXIDE SYNTHASES) and thereby prevent its substrate-enzyme combination with arachidonic acid and the formation of eicosanoids, prostaglandins, and thromboxanes.
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Cyclooxygenase 1 -- toxicity.   2012 1
Cyclooxygenase 2.   2010 1
 

Cyclooxygenase 2 antagonists & inhibitors -- See Cyclooxygenase 2 Inhibitors


A subclass of cyclooxygenase inhibitors with specificity for CYCLOOXYGENASE-2.
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Cyclooxygenase 2 Inhibitor -- See Cyclooxygenase 2 Inhibitors


A subclass of cyclooxygenase inhibitors with specificity for CYCLOOXYGENASE-2.
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Cyclooxygenase 2 Inhibitors.   2007 1
Cyclooxygenase 2 Inhibitors -- economics -- United States -- Statistics.   2006 1
Cyclooxygenase 2 -- toxicity.   2012 1
 

Cyclooxygenase Inhibitor -- See Cyclooxygenase Inhibitors


Compounds or agents that combine with cyclooxygenase (PROSTAGLANDIN-ENDOPEROXIDE SYNTHASES) and thereby prevent its substrate-enzyme combination with arachidonic acid and the formation of eicosanoids, prostaglandins, and thromboxanes.
  1
Cyclooxygenase Inhibitors.   2010 1
Cyclooxygenase Inhibitors -- adverse effects.   2
Cyclooxygenase Inhibitors -- Congresses.   2
Cyclooxygenase Inhibitors -- therapeutic use.   2
Cycloparaffins.   2
Cycloparaffins -- analysis.   2007 1
Cycloparaffins -- chemical synthesis.   1982 1
Cyclopentanes -- chemistry.   1971 1
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