Abraham Nudelman

ORCID: 0000-0001-8946-7288
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About
Contact & Profiles
Research Areas
  • Histone Deacetylase Inhibitors Research
  • Cancer therapeutics and mechanisms
  • Synthesis and Biological Evaluation
  • Carbohydrate Chemistry and Synthesis
  • Click Chemistry and Applications
  • Asymmetric Synthesis and Catalysis
  • Synthesis and biological activity
  • Chemotherapy-induced cardiotoxicity and mitigation
  • Synthesis of β-Lactam Compounds
  • Chemical Synthesis and Reactions
  • Chemical Synthesis and Analysis
  • Organic Chemistry Cycloaddition Reactions
  • Synthesis and Reactions of Organic Compounds
  • Analytical Chemistry and Chromatography
  • Epigenetics and DNA Methylation
  • Cancer Treatment and Pharmacology
  • Lung Cancer Research Studies
  • HIV/AIDS drug development and treatment
  • Synthetic Organic Chemistry Methods
  • Various Chemistry Research Topics
  • Biochemical and Molecular Research
  • Porphyrin and Phthalocyanine Chemistry
  • Retinoids in leukemia and cellular processes
  • Chemical Reaction Mechanisms
  • Organophosphorus compounds synthesis

Bar-Ilan University
2014-2024

Brooklyn College
2021

Alzheimer's Association of Israel
2015-2016

Tel Aviv University
1994-2009

Rabin Medical Center
2007-2008

Neurological Surgery
2007

University of California, San Francisco
2007

La Trobe University
2005

University of California, San Diego
2002

Scripps Research Institute
2002

ADVERTISEMENT RETURN TO ISSUEPREVNoteNEXTNMR Chemical Shifts of Common Laboratory Solvents as Trace ImpuritiesHugo E. Gottlieb, Vadim Kotlyar, and Abraham NudelmanView Author Information Department Chemistry, Bar-Ilan University, Ramat-Gan 52900, IsraelCite this: J. Org. Chem. 1997, 62, 21, 7512–7515Publication Date (Web):October 17, 1997Publication History Received27 June 1997Published online17 October inissue 1...

10.1021/jo971176v article EN The Journal of Organic Chemistry 1997-10-01

Tables of 1H and 13C NMR chemical shifts have been compiled for common organic compounds often used as reagents or found products contaminants in deuterated solvents. Building upon the work Gottlieb, Kotlyar, Nudelman Journal Organic Chemistry, signals impurities are now reported additional solvents (tetrahydrofuran-d8, toluene-d8, dichloromethane-d2, chlorobenzene-d5, 2,2,2-trifluoroethanol-d3) which frequently organometallic laboratories. Chemical other organics internal standards...

10.1021/om100106e article EN Organometallics 2010-04-16

Abstract Doxorubicin (Adriamycin) is one of the most commonly used chemotherapeutic drugs and exhibits a wide spectrum activity against solid tumors, lymphomas, leukemias. classified as topoisomerase II poison, although other mechanisms action have been characterized. Here, we show that doxorubicin-DNA adducts (formed by coadministration doxorubicin with non-toxic doses formaldehyde-releasing prodrugs) induce more cytotoxic response in HL-60 cells than single agent. Doxorubicin-DNA seem to...

10.1158/0008-5472.can-05-3410 article EN Cancer Research 2006-05-01

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTStudies in sugar chemistry. 2. A simple method for O-deacylation of polyacylated sugarsJacob Herzig, Abraham Nudelman, Hugo E. Gottlieb, and Bilha FischerCite this: J. Org. Chem. 1986, 51, 5, 727–730Publication Date (Print):March 1, 1986Publication History Published online1 May 2002Published inissue 1 March 1986https://pubs.acs.org/doi/10.1021/jo00355a026https://doi.org/10.1021/jo00355a026research-articleACS PublicationsRequest reuse...

10.1021/jo00355a026 article EN The Journal of Organic Chemistry 1986-03-01

Abstract Hydrogen chloride qualitatively generated in situ by the addition of acetyl to alcoholic solutions is a useful reagent for carboxylic acid esterification, N-t-Boc deprotection and phosphoramide solvolysis reactions.

10.1080/00397919808005101 article EN Synthetic Communications 1998-02-01

Abstract A novel derivative of butyric acid, pivalyloxymethyl butyrate (AN‐9) has been shown, in vitro , to: (a) induce cytodifferentiation and inhibit the proliferation leukemic cells; (b) growth formation Lewis lung carcinoma colonies semi‐solid agar. AN‐9 affect cells at about 10‐fold lower concentration a faster rate than does acid. The esters propionic, isobutyric valeric acids do not elicit effects similar to those AN‐9, while isobutyryloxymethyl does, which strongly suggests that...

10.1002/ijc.2910490113 article EN International Journal of Cancer 1991-08-19

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTOrganotin nucleophiles. 6. Palladium-catalyzed allylic etherification with tin alkoxidesEhud Keinan, Mahendra Sahai, Zeev Poth, Abraham Nudelman, and Jacob HerzigCite this: J. Org. Chem. 1985, 50, 19, 3558–3566Publication Date (Print):September 1, 1985Publication History Published online1 May 2002Published inissue 1 September 1985https://pubs.acs.org/doi/10.1021/jo00219a023https://doi.org/10.1021/jo00219a023research-articleACS PublicationsRequest...

10.1021/jo00219a023 article EN The Journal of Organic Chemistry 1985-09-01

The cascade of events that occurs in Alzheimer's disease involving oxidative stress and the reduction cholinergic transmission can be better addressed by multifunctional drugs than cholinesterase inhibitors alone. For this purpose, we prepared a large number derivatives indoline-3-propionic acids esters. They showed scavenging activity against different radicals solution significant protection cytotoxicity cardiomyocytes primary cultures neuronal cells exposed to H2O2 species serum...

10.1021/jm301411g article EN Journal of Medicinal Chemistry 2012-11-14

We describe the preparation and evaluation of novel indoline derivatives with potent antioxidant anti-inflammatory activities for treatment pathological conditions associated chronic inflammation. The indolines are substituted at position 1 chains carrying amino, ester, amide, or alcohol groups, some have additional substituents, Cl, MeO, Me, F, HO, BnO, on benzo ring. Concentrations pM to nM several compounds protected RAW264.7 macrophages against H2O2 induced cytotoxicity LPS elevation NO,...

10.1021/acs.jmedchem.8b00001 article EN Journal of Medicinal Chemistry 2018-04-22

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTNovel anticancer prodrugs of butyric acid. 2Abraham Nudelman, Margaretta Ruse, Adina Aviram, Ester Rabizadeh, Matityahu Shaklai, Yael Zimrah, and Ada RephaeliCite this: J. Med. Chem. 1992, 35, 4, 687–694Publication Date (Print):February 1, 1992Publication History Published online1 May 2002Published inissue 1 February 1992https://pubs.acs.org/doi/10.1021/jm00082a009https://doi.org/10.1021/jm00082a009research-articleACS PublicationsRequest reuse...

10.1021/jm00082a009 article EN Journal of Medicinal Chemistry 1992-02-01

Histone modification has emerged as a promising approach to cancer therapy. We explored the efficacy of novel class histone deacetylase inhibitors in treatment malignant gliomas. Treatment glioma cell lines with two butyric acid derivatives, pivaloylomethyl butyrate (AN-9) and butyroyloxymethyl (AN-1), induced hyperacetylation, increased p21(Cip1) expression, inhibited proliferation, enhanced apoptosis. inhibitor-induced apoptosis was mediated primarily by caspase-8. cells AN-1 or AN-9 for...

10.1158/1535-7163.mct-05-0087 article EN Molecular Cancer Therapeutics 2005-12-01

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTThe stereochemical course of ester-amide interchange leading to optically active phosphinic and sulfinic amidesAbraham Nudelman Donald J. CramCite this: Am. Chem. Soc. 1968, 90, 14, 3869–3870Publication Date (Print):July 1, 1968Publication History Published online1 May 2002Published inissue 1 July 1968https://pubs.acs.org/doi/10.1021/ja01016a053https://doi.org/10.1021/ja01016a053research-articleACS PublicationsRequest reuse permissionsArticle...

10.1021/ja01016a053 article EN Journal of the American Chemical Society 1968-07-01

We describe the synthesis, biological activities, and clinical applications of a novel family butyric acid (BA) prodrugs having general formula Me(CH2)2COOCH(R)OR1, where R = H, Me, Pr, tert-Bu; R1 OC-alkyl, OC-Ar, OC-heterocycles , P(O)(OEt)2. These acyloxyalkyl serve as molecular devices for efficient transport BA into cells, leading to significant increase in its potency. The were studied anticancer activity, induction hemoglobin (Hb) expression protection hair follicles from damage...

10.1002/1098-2299(200007/08)50:3/4<379::aid-ddr20>3.0.co;2-8 article EN Drug Development Research 2000-01-01

The syn-rotamers of carbamate derivatives α-amino acids are shown to be stabilized by the formation H-bond complexes with carboxylic acid moieties in solution. This effect is, as expected, concentration and temperature dependent. Thermodynamic parameters (both ΔG° ΔG‡) for N-Boc-alanine were determined NMR ±60 °C range.

10.1021/jo961446u article EN The Journal of Organic Chemistry 1996-01-01

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTA novel method for stereoselective glucuronidationBilha Fischer, Abraham Nudelman, Margareta Ruse, Jacob Herzig, Hugo E. Gottlieb, and Ehud KeinanCite this: J. Org. Chem. 1984, 49, 25, 4988–4993Publication Date (Print):December 1, 1984Publication History Published online1 May 2002Published inissue 1 December 1984https://pubs.acs.org/doi/10.1021/jo00199a046https://doi.org/10.1021/jo00199a046research-articleACS PublicationsRequest reuse...

10.1021/jo00199a046 article EN The Journal of Organic Chemistry 1984-12-01

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTEnthalpies of transfer transition states in the Menshutkin reaction from a polar protic to dipolar aprotic solventPaul Haberfield, Abraham Nudelman, Allen Bloom, Richard Romm, and Henry GinsbergCite this: J. Org. Chem. 1971, 36, 13, 1792–1795Publication Date (Print):July 1, 1971Publication History Published online1 May 2002Published inissue 1 July 1971https://pubs.acs.org/doi/10.1021/jo00812a016https://doi.org/10.1021/jo00812a016research-articleACS...

10.1021/jo00812a016 article EN The Journal of Organic Chemistry 1971-07-01

The novel prodrug of butyric acid (BA), pivaloyloxymethyl butyrate, has been shown, in vitro, to induce differentiation and inhibit leukemic cell proliferation. affects the cells vitro at lower concentration least 100 times faster than does (BA). We have compared ability BA with that its AN‐9 modulate expression early regulating genes, c‐ myc jun , HL‐60 cells. Exposure resulted a decrease an increase expression. elicited this effect concentrations BA. Since changes occur minutes after...

10.1016/0014-5793(93)80932-k article EN FEBS Letters 1993-08-16
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