sodium cyclohexylsulfamate (sodium cyclamate)

ID: ALA273977

Chembl Id: CHEMBL273977

Cas Number: 139-05-9

PubChem CID: 23665706

Product Number: S109887

Max Phase: Phase

Molecular Formula: C6H12NNaO3S

Molecular Weight: 201.22

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Synonyms: Sodium cyclamate | SODIUM CYCLAMATE|139-05-9|Sodium N-cyclohexylsulfamate|Sodium cyclohexylsulfamate|Cyclamic acid sodium salt|Sucaryl sodium|Sodium cyclohexanesulfamate|Cyclamate sodium|Sulfamic acid, cyclohexyl-, monosodium salt|Cyclamate, sodium|Assugrin|Asugryn|Ibiosuc|Suessette|Suestamin|Sugarin|Sugaron|Sodium sucaryl|Dulzor-Etas|Hachi-Sugar|Sucrum 7|Cyclamate, sodium salt|Natriumzyklamate|Cyclohexylsulfamate sodium|CHEBI:82431|Cyclamate sodium/ saccharin sodium|Cyclamic acid (sodium)|1I6F4Show More

Canonical SMILES:  O=S(=O)([O-])NC1CCCCC1.[Na+]

Standard InChI:  InChI=1S/C6H13NO3S.Na/c8-11(9,10)7-6-4-2-1-3-5-6;/h6-7H,1-5H2,(H,8,9,10);/q;+1/p-1

Standard InChI Key:  UDIPTWFVPPPURJ-UHFFFAOYSA-M

Alternative Forms

  1. Parent:

Associated Targets(Human)

Homo sapiens (32628 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA9 Tclin Carbonic anhydrase IX (8255 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA7 Tclin Carbonic anhydrase VII (2318 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA2 Tclin Carbonic anhydrase II (17698 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA1 Tclin Carbonic anhydrase I (13240 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA12 Tclin Carbonic anhydrase XII (6231 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA14 Tclin Carbonic anhydrase XIV (1305 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TAS2R41 Tchem Taste receptor type 2 member 41 (57 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TAS2R19 Tchem Taste receptor type 2 member 19 (20 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Rattus norvegicus (775804 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mus musculus (284745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: YesAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Calculated Properties

Molecular Weight: 201.22Molecular Weight (Monoisotopic): 201.0436AlogP: #Rotatable Bonds:
Polar Surface Area: Molecular Species: HBA: HBD:
#RO5 Violations: HBA (Lipinski): HBD (Lipinski): #RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: CX LogP: CX LogD:
Aromatic Rings: Heavy Atoms: QED Weighted: Np Likeness Score:

References

1. Wiley RA, Pearson DA, Schmidt V, Wesche SB, Roxon JJ..  (1983)  Synthesis and bacterial metabolism of cis- and trans-2-alkyl analogues of sodium cyclamate.,  26  (7): [PMID:6191033] [10.1021/jm00361a025]
2. DuBois GE, Stephenson RA..  (1985)  Diterpenoid sweeteners. Synthesis and sensory evaluation of stevioside analogues with improved organoleptic properties.,  28  (1): [PMID:3965718] [10.1021/jm00379a017]
3. Talevi A, Enrique AV, Bruno-Blanch LE..  (2012)  Anticonvulsant activity of artificial sweeteners: a structural link between sweet-taste receptor T1R3 and brain glutamate receptors.,  22  (12): [PMID:22579423] [10.1016/j.bmcl.2012.04.076]
4. USP Dictionary of USAN and International Names (2010 edition) and USAN registrations 2007-date, 
5. PubChem BioAssay data set, 
6. Villalba ML, Palestro P, Ceruso M, Gonzalez Funes JL, Talevi A, Bruno Blanch L, Supuran CT, Gavernet L..  (2016)  Sulfamide derivatives with selective carbonic anhydrase VII inhibitory action.,  24  (4): [PMID:26795114] [10.1016/j.bmc.2016.01.012]
7.  (2013)  Methods To Identify Modulators, 
8.  (2013)  Methods To Identify Modulators of TAS2R48 Receptors,