S-[4-[(4-Nitrobenzyl)oxy]phenethyl]isothiourea Methanesulfonate - >98.0%(HPLC), high purity , CAS No.182004-65-5, Channel blocker of TRPC3;Channel blocker of TRPC5;Channel blocker of TRPC6

Item Number
S161158
Grouped product items
SKUSizeAvailabilityPrice Qty
S161158-10mg
10mg
In stock
$109.90
S161158-50mg
50mg
In stock
$391.90
S161158-100mg
100mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$705.90

NCX inhibitor. TRPC blocker.

Basic Description

SynonymsGTPL4232 | HY-15415 | s4643 | 2-[2-[4-(4-NITROBENZYLOXY)PHENYL]ETHYL]ISOTHIOUREA MESYLATE | CS-0848 | 2-(2-(4-(4-nitrobenzyloxy)phenyl)ethyl)isothiourea mesylate | C17H21N3O6S2 | methanesulfonic acid;2-[4-[(4-nitrophenyl)methoxy]phenyl]ethyl carbamimidoth
Specifications & Purity>98.0%(HPLC)
Storage TempStore at -20°C
Shipped InIce chest + Ice pads
GradeMoligand™
Action TypeCHANNEL BLOCKER
Mechanism of actionChannel blocker of TRPC3;Channel blocker of TRPC5;Channel blocker of TRPC6
Product Description

KB-R7943 mesylate is a widely used inhibitor of the reverse Na+/Ca2+ exchanger (NCXrev) with IC50 of 5.7±2.1 μM. KB-R7943 mesylate induces cancer cell death via activating the JNK pathway and blocking autophagic flux.

Associated Targets(Human)

TRPC3 Tchem Short transient receptor potential channel 3 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
TRPC5 Tchem Short transient receptor potential channel 5 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
TRPC6 Tchem Short transient receptor potential channel 6 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name methanesulfonic acid;2-[4-[(4-nitrophenyl)methoxy]phenyl]ethyl carbamimidothioate
INCHI InChI=1S/C16H17N3O3S.CH4O3S/c17-16(18)23-10-9-12-3-7-15(8-4-12)22-11-13-1-5-14(6-2-13)19(20)21;1-5(2,3)4/h1-8H,9-11H2,(H3,17,18);1H3,(H,2,3,4)
InChi Key WGIKEBHIKKWJLG-UHFFFAOYSA-N
Canonical SMILES CS(=O)(=O)O.C1=CC(=CC=C1CCSC(=N)N)OCC2=CC=C(C=C2)[N+](=O)[O-]
Isomeric SMILES CS(=O)(=O)O.C1=CC(=CC=C1CCSC(=N)N)OCC2=CC=C(C=C2)[N+](=O)[O-]
PubChem CID 9823846
Molecular Weight 427.49
Reaxy-Rn 9099076

Certificates

Certificate of Analysis(COA)

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2 results found

Lot NumberCertificate TypeDateItem
D2102236Certificate of AnalysisJan 02, 2024 S161158
D2102237Certificate of AnalysisJan 02, 2024 S161158

Chemical and Physical Properties

Sensitivityheat sensitive

Safety and Hazards(GHS)

Reaxy-Rn 9099076

Related Documents

References

1. Wong RW et al..  (2020)  An activator of G protein-coupled receptor and MEK1/2-ERK1/2 signaling inhibits HIV-1 replication by altering viral RNA processing..  PLoS Pathog,  16  (2): (e1008307).  [PMID:32069328]
2. Wong RW et al..  (2018)  Cardiac glycoside/aglycones inhibit HIV-1 gene expression by a mechanism requiring MEK1/2-ERK1/2 signaling..  Sci Rep,  (850).  [PMID:29339801]
3. Sherkhane P & Kapfhammer JP.  (2017)  Chronic pharmacological blockade of the Na(+) /Ca(2+) exchanger modulates the growth and development of the Purkinje cell dendritic arbor in mouse cerebellar slice cultures..  Eur J Neurosci,      [PMID:28715135]
4. Di Giuro CML et al..  (2017)  Na +/Ca2+ exchangers and Orai channels jointly refill endoplasmic reticulum (ER) Ca2+ via ER nanojunctions in vascular endothelial cells..  Pflugers Arch,  469  (10): (1287-1299).  [PMID:28497275]

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