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· · COA & SDS available for every product · Same-day shipping on in-stock items DPO-1 - Moligand™, ≥98% , Channel blocker of K v1.5, CAS No.43077-30-1, Channel blocker of K v1.5
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥98% Synonyms
p-(2-Hydroxy-1-naphthylazo)benzenesulfonic acid sodium salt | SDCCGSBI-0633727.P001 | LP00543 | UNII-H9LQP293GK | Q27165442 | DPO 1 | DPO1 | DPO-1 | HMS3413F13 | Neomenthyldiphenylphosphine oxide | DTXSID10616838 | W-105388 | BPCNGVCAHAIZEE-COPCDDAFSA-N |
Storage
Protected from light,Store at -20°C
Shipped In
Ice chest + Ice pads
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Why this grade Moligand™, ≥98% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Protected from light,Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Synonyms
p-(2-Hydroxy-1-naphthylazo)benzenesulfonic acid sodium salt | SDCCGSBI-0633727.P001 | LP00543 | UNII-H9LQP293GK | Q27165442 | DPO 1 | DPO1 | DPO-1 | HMS3413F13 | Neomenthyldiphenylphosphine oxide | DTXSID10616838 | W-105388 | BPCNGVCAHAIZEE-COPCDDAFSA-N |
Specifications & Purity
Moligand™, ≥98%
Biochemical and Physiological Mechanisms
DPO-1 is an inhibitor of human Kv1.5 potassium channel; representative blocker of a novel pharmacophore. The Kv1.5 potassium channel, which underlies the ultrarapid delayed rectifier current, IKur, is reported to be enriched in human atrium versus ventric
Storage
Protected from light, Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Action Type
CHANNEL BLOCKER
Mechanism of action
Channel blocker of K v1.5
Names and Identifiers Pubchem Sid 504769020 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504769020 Canonical Smiles CC1CCC(C(C1)P(=O)(C2=CC=CC=C2)C3=CC=CC=C3)C(C)C IUPAC Name [[(1S,2S,5R)-5-methyl-2-propan-2-ylcyclohexyl]-phenylphosphoryl]benzene InChIKey BPCNGVCAHAIZEE-COPCDDAFSA-N INCHI 1S/C22H29OP/c1-17(2)21-15-14-18(3)16-22(21)24(23,19-10-6-4-7-11-19)20-12-8-5-9-13-20/h4-13,17-18,21-22H,14-16H2,1-3H3/t18-,21+,22+/m1/s1 Isomeric SMILES C[C@@H]1CC[C@H]([C@H](C1)P(=O)(C2=CC=CC=C2)C3=CC=CC=C3)C(C)C Molecular Weight 340.44 Reaxy-Rn 10267089 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=10267089&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Lipids and lipid-like molecules Class Prenol lipids Subclass Monoterpenoids Intermediate Tree Nodes Not available Direct Parent Aromatic monoterpenoids Alternative Parents Monocyclic monoterpenoids Menthane monoterpenoids Phenylphosphines and derivatives Organopnictogen compounds Organophosphorus compounds Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic homomonocyclic compounds Substituents P-menthane monoterpenoid - Monocyclic monoterpenoid - Aromatic monoterpenoid - Phenylphosphine - Benzenoid - Monocyclic benzene moiety - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organophosphorus compound - Aromatic homomonocyclic compound Description This compound belongs to the class of organic compounds known as aromatic monoterpenoids. These are monoterpenoids containing at least one aromatic ring. External Descriptors Not available 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.
3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Solubility Solvent:ethanol, Max Conc. mg/mL: 34.04, Max Conc. mM: 100 Sensitivity light sensitive Molecular Weight 340.400 g/mol XLogP3 6.000 Hydrogen Bond Donor Count 0 Hydrogen Bond Acceptor Count 1 Rotatable Bond Count 4 Exact Mass 340.196 Da Monoisotopic Mass 340.196 Da Topological Polar Surface Area 17.100 Ų Heavy Atom Count 24 Formal Charge 0 Complexity 409.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 3 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 1
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Reconstitution Calculator Reviews Need help choosing the grade? Our grade selection guide covers purity, stabilizer status, and application suitability for all variants in our catalog.
View Moligand™ grade guide →
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