DIDS - Moligand™ , Channel blocker of CaCC;Channel blocker of ClC-6;Channel blocker of ClC-7;Channel blocker of ClC-Ka;Channel blocker of ClC-Kb, CAS No.53005-05-3, Channel blocker of CaCC;Channel blocker of ClC-6;Channel blocker of ClC-7;Channel blocker of ClC-Ka;Channel blocker of ClC-Kb

CAS: 53005-05-3 Cat. No.: D609876 Número EC: 674-295-5 PubChem CID: 40600

GRADE & PURITY Moligand™

Synonyms

DTXSID20164976 | GTPL4177 | QHR3Z2PN8M | ABC inhibitor 2 | UNII-QHR3Z2PN8M | Benzenesulfonic acid, 2,2'-(1,2-ethenediyl)bis[5-isothiocyanato- | FT-0617065 | Benzenesulfonic acid, 2,2'-[1,2-ethenediyl]bis[5-isothiocyanato- | DTXSID701027549 | 5-isothiocyan

Storage

Room temperature

Specifications

Sinónimos

DTXSID20164976 | GTPL4177 | QHR3Z2PN8M | ABC inhibitor 2 | UNII-QHR3Z2PN8M | Benzenesulfonic acid, 2, 2'-(1, 2-ethenediyl)bis[5-isothiocyanato- | FT-0617065 | Benzenesulfonic acid, 2, 2'-[1, 2-ethenediyl]bis[5-isothiocyanato- | DTXSID701027549 | 5-isothiocyan

Especificaciones y pureza

Moligand™

Condiciones de almacenamiento de almacenamiento

Room temperature

Grado

Moligand™

Tipo de acción

CHANNEL BLOCKER

Mecanismo de acción

Channel blocker of CaCC;Channel blocker of ClC-6;Channel blocker of ClC-7;Channel blocker of ClC-Ka;Channel blocker of ClC-Kb

Nombres e identificadores

• Sonrisas canónicas: S=C=Nc1ccc(c(c1)S(=O)(=O)O)C=Cc1ccc(cc1S(=O)(=O)O)N=C=S
• IUPAC Name: 5-isothiocyanato-2-[2-(4-isothiocyanato-2-sulfophenyl)ethenyl]benzene-1-sulfonic acid
• InChIKey: YSCNMFDFYJUPEF-UHFFFAOYSA-N
• INCHI: 1S/C16H10N2O6S4/c19-27(20,21)15-7-13(17-9-25)5-3-11(15)1-2-12-4-6-14(18-10-26)8-16(12)28(22,23)24/h1-8H,(H,19,20,21)(H,22,23,24)
• Isómeros SMILES: C1=CC(=C(C=C1N=C=S)S(=O)(=O)O)C=CC2=C(C=C(C=C2)N=C=S)S(=O)(=O)O
• PubChem CID: 40600

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Phenylpropanoids and polyketides
    • Clase Stilbenes
      • Subclass Sulfonated stilbenes

• Kingdom: Organic compounds
• Superclass: Phenylpropanoids and polyketides
• Clase: Stilbenes
• Subclass: Sulfonated stilbenes
• Intermediate Tree Nodes: Not available
• Direct Parent: Sulfonated stilbenes
• Alternative Parents: Benzenesulfonic acids and derivatives Benzenesulfonyl compounds 1-sulfo,2-unsubstituted aromatic compounds Styrenes Sulfonyls Organosulfonic acids Isothiocyanates Propargyl-type 1,3-dipolar organic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Sulfonated stilbene - Benzenesulfonate - Arylsulfonic acid or derivatives - Benzenesulfonyl group - 1-sulfo,2-unsubstituted aromatic compound - Styrene - Monocyclic benzene moiety - Benzenoid - Organic sulfonic acid or derivatives - Sulfonyl - Organosulfonic acid - Organosulfonic acid or derivatives - Isothiocyanate - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organosulfur compound - Organonitrogen compound - Organopnictogen compound - Organic oxygen compound - Aromatic homomonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as sulfonated stilbenes. These are stilbenes that carry a sulfone group at one or more positions of either benzene rings.
• External Descriptors: arenesulfonic acid

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Objetivos asociados (humanos)

RAD1 Tchem Cell cycle checkpoint protein RAD1 (0 Activities)

Discover Target: RAD1

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

ANO1 Tclin Anoctamin-1 (0 Activities)

Discover Target: ANO1

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

CLCNKB Tchem Chloride channel protein ClC-Kb (0 Activities)

Discover Target: CLCNKB

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

CLCN6 Tchem Chloride transport protein 6 (1 Activities)

Discover Target: CLCN6

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

CLCN7 Tchem H(+)/Cl(-) exchange transporter 7 (1 Activities)

Discover Target: CLCN7

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

CLCNKA Tchem Chloride channel protein ClC-Ka (0 Activities)

Discover Target: CLCNKA

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

Propiedades químicas y físicas

• Peso molecular: 454.500 g/mol
• XLogP3: 4.500
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 10
• Rotatable Bond Count: 6
• Exact Mass: 453.942 Da
• Monoisotopic Mass: 453.942 Da
• Topological Polar Surface Area: 214.000 Ų
• Heavy Atom Count: 28
• Formal Charge: 0
• Complexity: 818.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 1
• The total count of all stereochemical bonds: 1
• Covalently-Bonded Unit Count: 1

Referencias

1. Lai Cuixin, Yang Lina, Pathiranage Vishaka, Wang Ruizhao, Subach Fedor V., Walker Alice R., Piatkevich Kiryl D..  (2024)  Genetically encoded green fluorescent sensor for probing sulfate transport activity of solute carrier family 26 member a2 (Slc26a2) protein.  Communications Biology,  7  (1): (1-13).  [PMID:39443638] [10.1038/s42003-024-07020-9]

2. Jie Zhong, Hang Wei, Jian-Xiong Xie, Yu-Hui Wu, Bing Tang, Qi Zou, Peng-Ran Guo, Zhi-Liang Chen.  (2024)  Uptake, subcellular distribution, and fate of tetracycline in two wetland plants supplemented with microbial agents: Effect and mechanism.  JOURNAL OF ENVIRONMENTAL MANAGEMENT,      [PMID:38879966] [10.1016/j.jenvman.2024.121428]