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· · COA & SDS available for every product · Same-day shipping on in-stock items SF1670 - ≥98% , CAS No.345630-40-2
Synonyms
N-(9,10-dioxo-9,10-dihydrophenanthren-2-yl)pivalamide | N-(9,10-dihydro-9,10-dioxophenanthren-7-yl)pivalamide | CCG-267547 | Histidine, monohydrochloride, monohydrate | HY-15842 | N-(9,10-dihydro-9,10-dioxophethren-7-yl)pivalamide | Protein Tyrosine Phosp
Storage
Store at 2-8°C,Desiccated
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Why this grade ≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at 2-8°C,Desiccated Ships Wet ice 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.
Overview Product introduction
SF1670 is a potent and specific phosphatase and tensin homolog deleted on chromosome 10 (PTEN) inhibitor
Store at +4°C. Store under desiccating conditions. The product can be stored for up to 12 months.
Application
SF1670 has been used:
• To study the effect of microRNA-30a on PTEN (phosphatase and tensin homologue deleted on chromosome 10 ) expression regulation.
• To study the formation of autophagosomes, induced by EGF (Epidermal growth factor) - dependent PTEN expression.
• To study the role of PTEN in the regulation of autophagy induction in human normal endometrial stromal cells.
Specifications Synonyms
N-(9, 10-dioxo-9, 10-dihydrophenanthren-2-yl)pivalamide | N-(9, 10-dihydro-9, 10-dioxophenanthren-7-yl)pivalamide | CCG-267547 | Histidine, monohydrochloride, monohydrate | HY-15842 | N-(9, 10-dihydro-9, 10-dioxophethren-7-yl)pivalamide | Protein Tyrosine Phosp
Specifications & Purity
≥98%
Storage
Store at 2-8°C, Desiccated
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Note
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Names and Identifiers Pubchem Sid 504765103 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504765103 Canonical Smiles CC(C)(C)C(=O)NC1=CC2=C(C=C1)C3=CC=CC=C3C(=O)C2=O IUPAC Name N-(9,10-dioxophenanthren-2-yl)-2,2-dimethylpropanamide InChIKey VZQDDSYKVYARDW-UHFFFAOYSA-N INCHI 1S/C19H17NO3/c1-19(2,3)18(23)20-11-8-9-13-12-6-4-5-7-14(12)16(21)17(22)15(13)10-11/h4-10H,1-3H3,(H,20,23) Isomeric SMILES CC(C)(C)C(=O)NC1=CC2=C(C=C1)C3=CC=CC=C3C(=O)C2=O PubChem CID 9926586 Molecular Weight 307.35
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 Benzenoids Class Phenanthrenes and derivatives Subclass Phenanthraquinones Intermediate Tree Nodes Not available Direct Parent Phenanthraquinones Alternative Parents Hydrophenanthrenes Naphthalenes O-quinones N-arylamides Aryl ketones Secondary carboxylic acid amides Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic homopolycyclic compounds Substituents Phenanthraquinone - Hydrophenanthrene - Naphthalene - O-quinone - Quinone - N-arylamide - Aryl ketone - Ketone - Secondary carboxylic acid amide - Carboxamide group - Carboxylic acid derivative - Carbonyl group - Organic oxide - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Aromatic homopolycyclic compound Description This compound belongs to the class of organic compounds known as phenanthraquinones. These are phenanthrene derivatives containing two ketone groups at position C9 and C10, respectively. 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 Soluble in DMSO to 100 mM Molecular Weight 307.300 g/mol XLogP3 3.100 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 3 Rotatable Bond Count 2 Exact Mass 307.121 Da Monoisotopic Mass 307.121 Da Topological Polar Surface Area 63.200 Ų Heavy Atom Count 23 Formal Charge 0 Complexity 519.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 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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