Target type: molecularfunction
Binding to an organic cyclic compound, any molecular entity that contains carbon arranged in a cyclic molecular structure. [GOC:sjw, PMID:7583672]
Organic cyclic compound binding refers to the interaction of a molecule with a cyclic organic compound. Cyclic organic compounds are molecules that contain a closed ring structure, formed by three or more atoms, often including carbon, oxygen, nitrogen, or sulfur. These interactions are essential for various biological processes, including:
1. **Signal Transduction:** Cyclic compounds like cyclic nucleotides (cAMP, cGMP) act as second messengers, relaying signals from receptors to downstream effector proteins. They bind to specific proteins, altering their activity and mediating cellular responses.
2. **Enzyme Catalysis:** Many enzymes require the binding of specific cyclic compounds as cofactors or substrates. For instance, NAD+ (nicotinamide adenine dinucleotide) and FAD (flavin adenine dinucleotide), which are important electron carriers in metabolism, have cyclic structures.
3. **DNA and RNA Binding:** Cyclic compounds like purines and pyrimidines are the building blocks of DNA and RNA. These molecules form specific interactions with each other, stabilizing the double helix structure of DNA and RNA.
4. **Drug Targeting:** Many pharmaceuticals exploit the ability of cyclic compounds to bind to specific targets within the body. For example, antibiotics like penicillin target bacterial enzymes involved in cell wall synthesis, and anti-cancer drugs like cisplatin bind to DNA, inhibiting cell division.
5. **Cellular Structure:** Cyclic compounds contribute to the structure and stability of membranes and other cellular components. For example, phospholipids, which form the cell membrane, contain cyclic structures.
The binding of cyclic compounds can occur through various non-covalent interactions, including hydrogen bonding, van der Waals forces, hydrophobic interactions, and electrostatic interactions. The specific interactions and binding affinity depend on the chemical structure of the compound and the binding site on the target molecule. These interactions are often highly specific, enabling the recognition and regulation of specific biological processes.'
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Protein | Definition | Taxonomy |
---|---|---|
Synaptic vesicular amine transporter | A synaptic vesicular amine transporter that is encoded in the genome of cow. [OMA:Q27963, PRO:DNx] | Bos taurus (cattle) |
Monocarboxylate transporter 1 | A monocarboxylate transporter 1 that is encoded in the genome of human. [PRO:DNx, UniProtKB:P53985] | Homo sapiens (human) |
Melatonin receptor type 1A | A melatonin receptor type 1A that is encoded in the genome of human. [PRO:WCB, UniProtKB:P48039] | Homo sapiens (human) |
Compound | Definition | Classes | Roles |
---|---|---|---|
melatonin | acetamides; tryptamines | anticonvulsant; central nervous system depressant; geroprotector; hormone; human metabolite; immunological adjuvant; mouse metabolite; radical scavenger | |
methylbufotenin | 5-methoxy-N,N-dimethyltryptamine : A tryptamine alkaloid that is N,N-dimethyltryptamine substituted by a methoxy group at position 5. | aromatic ether; tertiary amino compound; tryptamine alkaloid | hallucinogen; plant metabolite |
6-chloromelatonin | acetamides | ||
6-hydroxymelatonin | 6-hydroxymelatonin : A member of the class of tryptamines that is melatonin with a hydroxy group substituent at position 6. | acetamides; tryptamines | metabolite; mouse metabolite |
reserpine | reserpine : An alkaloid found in the roots of Rauwolfia serpentina and R. vomitoria. Reserpine: An alkaloid found in the roots of Rauwolfia serpentina and R. vomitoria. Reserpine inhibits the uptake of norepinephrine into storage vesicles resulting in depletion of catecholamines and serotonin from central and peripheral axon terminals. It has been used as an antihypertensive and an antipsychotic as well as a research tool, but its adverse effects limit its clinical use. | alkaloid ester; methyl ester; yohimban alkaloid | adrenergic uptake inhibitor; antihypertensive agent; EC 3.4.21.26 (prolyl oligopeptidase) inhibitor; environmental contaminant; first generation antipsychotic; plant metabolite; xenobiotic |
tetrabenazine | 9,10-dimethoxy-3-isobutyl-1,3,4,6,7,11b-hexahydro-2H-pyrido[2,1-a]isoquinolin-2-one : A benzoquinolizine that is 1,2,3,4,4a,9,10,10a-octahydrophenanthrene in which the carbon at position 10a is replaced by a nitrogen and which is substituted by an isobutyl group at position 2, an oxo group at position 3, and methoxy groups at positions 6 and 7. | benzoquinolizine; cyclic ketone; tertiary amino compound | |
catechin | (+)-catechin : The (+)-enantiomer of catechin and a polyphenolic antioxidant plant metabolite. catechin : Members of the class of hydroxyflavan that have a flavan-3-ol skeleton and its substituted derivatives. Catechin: An antioxidant flavonoid, occurring especially in woody plants as both (+)-catechin and (-)-epicatechin (cis) forms. rac-catechin : A racemate comprising equimolar amounts of (+)- and (-)-catechin | catechin | antioxidant; plant metabolite |
4,4'-bisphenol f | 4,4'-bisphenol F: RN given refers to parent cpd bisphenol F : A bisphenol that is methane in which two of the hydrogens have been replaced by 4-hydroxyphenyl groups. | bisphenol; diarylmethane | environmental food contaminant; xenoestrogen |
reserpic acid | reserpic acid: inhibitor of norepinephrine transport into chromaffin vesicle ghosts; RN given refers to (3beta,16beta,17alpha,18beta,20alpha)-isomer parent cpd; structure given in first source | yohimban alkaloid | |
s20098 | acetamides | ||
6-methoxy-2,3,4,9-tetrahydropyrido[3,4-b]indol-1-one | beta-carbolines | ||
2-iodomelatonin | acetamides | ||
luzindole | luzindole : A member of the class of indoles that is tryptamine in which one of the amino hydrogens is replaced by an acetyl group while the hydrogen at position 2 is replaced by a benzyl group. luzindole: melatonin receptor antagonist; structure given in first source | acetamides; indoles | melatonin receptor antagonist |
2-bromomelatonin | 2-bromomelatonin: structure given in first source | ||
5-methoxyluzindole | |||
n-cyclopropylcarbonyl-2-(7-methoxy-1-naphthyl)ethylamine | N-cyclopropylcarbonyl-2-(7-methoxy-1-naphthyl)ethylamine: a highly potent & selective melatoninergic agonist; structure given in first source | ||
ramelteon | ramelteon: melatonin MT1/MT2 receptor agonist | indanes | |
a-130a | |||
aurapten | aurapten: RN refers to (E)-isomer; structure given in first source auraptene : A member of the class of coumarins that is umbelliferone in which the phenolic hydrogen has been replaced by a geranyl group. Ii is isolated from several edible fruits and vegetables and exhibits a variety of therapeutic properties. | coumarins; monoterpenoid | antihypertensive agent; antineoplastic agent; antioxidant; apoptosis inducer; dopaminergic agent; EC 2.7.11.24 (mitogen-activated protein kinase) inhibitor; gamma-secretase modulator; gastrointestinal drug; hepatoprotective agent; matrix metalloproteinase inhibitor; neuroprotective agent; plant metabolite; PPARalpha agonist; vulnerary |
umbelliprenin | umbelliprenin: RN given refers to cpd with unspecified isomeric designation | terpene lactone | |
ah 001 | AH 001: structure given in first source; a melatonin agonist | ||
4-phenyl-2-propionamidotetraline | 4-phenyl-2-propionamidotetraline: melatonin receptor antagonist; structure in first source | tetralins | |
2-phenylmelatonin | phenylindole | ||
iik7 | IIK7: structure in first source | ||
5-methoxycarbonylamino-n-acetyltryptamine | 5-methoxycarbonylamino-N-acetyltryptamine: an mt1/MT2 receptor agonist | acetamides | |
8-methoxy-2-propionamidotetralin | 8-methoxy-2-propionamidotetralin: enhances sperm hyperactivation via the MT1 receptor | tetralins | |
k 185 | |||
4-n-butyl-1-(4-(2-methylphenyl)-4-oxo-1-butyl)-piperidine hydrogen chloride | |||
ar c155858 | AR C155858: an MCT1 inhibitor; structure in first source | ||
azd3965 | AZD3965: a monocarboxylate transporter-1 inhibitor with antineoplastic activity; structure in first source | ||
ucm 454 | |||
5-hydroxyethoxy-n-acetyltryptamine | 5-hydroxyethoxy-N-acetyltryptamine: structure in first source | ||
4'-geranyloxyferulic acid | 4'-geranyloxyferulic acid: a colon cancer chemopreventive agent isolated from grapefruit skin; structure in first source |