Biological implications of the reaction possibilities of the proximate carcinogenic compound, N-hydroxy-2-fluorenylacetamide.

DOI: 10.1002/bms.1200030105

Source and publish data:

Biomedical mass spectrometry p. 21 - 27 (1976)

Update date:2022-08-05

Topics:

Authors:

Lhoest Lhoest

Razzouk Razzouk

Mercier Mercier

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1002/bms.1200030105

The biological implications, the reaction possibilities and the structure of different derivatives of N-hydroxy-2-fluorenylacetamide have been described.

Full text of DOI:10.1002/bms.1200030105

Products guided by the article

Product name:N-(9H-Fluoren-2-yl)-2,2,2-trifluoro-N-(2,2,2-trifluoro-acetoxy)-acetamide

Cas No:61144-85-2

R&D Labs maybe for 61144-85-2

Suzhou Lixin Pharmaceutical Co., Ltd.

Contact:86-512-88169812

Address:21 Tangxi Road, Suzhou New District, Suzhou 215151
Hangzhou Eastbiopharm Co.,Ltd.

Contact:+86-571-88931780

Address:Hangzhou,China
Chengdu Aslee Biopharmaceuticals, Inc

Contact:18608018419

Address:Chengdu Aslee Biopharmaceuticals, Inc
Tianjin Tensing Fine Chemical Research Develop Centre

Contact:86-022-23718576,13032267585

Address:2-2-201,13 Guiyuan road,Huayuan Industry district,Tianjin,china
ShanDong XinDa Chemical CO.,LTD(expird)

Contact:086-0311-87580543

Address:No.168, High Technology Development Zone Jinan Shandong China

Relevant to this article

Doi:10.1007/BF00904489
(1976)
A Potent Glucose-Platinum Conjugate Exploits Glucose Transporters and Preferentially Accumulates in Cancer Cells

Doi:10.1002/anie.201510551
(2016)
Transfer hydrogenation in water: Enantioselective, catalytic reduction of α-cyano and α-nitro substituted acetophenones

Doi:10.1021/ol1008894
(2010)
Doi:10.1039/jr9570001701
(1957)
Synthesis and characterization of N-(o-vanillinidene)-p-anisidine and N,N′-bis(o-vanillinidene)ethylenediamine and their metal complexes

Doi:10.1081/SIM-120021648
(2003)
Mass spectrometric analysis of purine de novo biosynthesis intermediates

Doi:10.1371/journal.pone.0208947
(2018)

Article Doi