Shanghai Nianxing Industrial Co., Ltd
China
Product Name: 1,N6-Ethenoadenosine
Price:
Purity: 95.0%
Stocking Period: 10 Day
Contact: Yang

Dayang Chem (Hangzhou) Co., Ltd.
China
Product Name: 1 N6-ETHENOADENOSINE FREE BASE
Price: $Inquiry/100g $Inquiry/1kg $Inquiry/100kg $Inquiry/1000kg
Purity: 98.0%
Stocking Period: Inquiry
Contact: Ms Wang

39007-51-7

39007-51-7 structure

Name: 1,N6-Ethenoadenosine
Chemical Name: 1 n6-ethenoadenosine free base
CAS Number: 39007-51-7
Molecular Formula: C₁₂H₁₃N₅O₄
Molecular Weight: 291.26
Catalog: Signaling Pathways Cell Cycle/DNA Damage Nucleoside Antimetabolite/Analog
Create Date: 2017-09-02 18:23:54
Modify Date: 2024-01-05 07:15:10
1,N6-Ethenoadenosine is a purine nucleoside analogue. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc[1].

Name	1 n6-ethenoadenosine free base
Synonyms	Ethenoadenosine N6-Ethenoadenosine 1,N6-ethanoadenosine 1,N6-etheno-adenosine

Description	1,N6-Ethenoadenosine is a purine nucleoside analogue. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc[1].
Related Catalog	Signaling Pathways >> Cell Cycle/DNA Damage >> Nucleoside Antimetabolite/Analog Research Areas >> Others
References	[1]. Robak T, Robak P. Purine nucleoside analogs in the treatment of rarer chronic lymphoid leukemias. Curr Pharm Des. 2012;18(23):3373-88.

Density	1.99g/cm3
Molecular Formula	C₁₂H₁₃N₅O₄
Molecular Weight	291.26
Exact Mass	291.09700
PSA	117.93000
Index of Refraction	1.915

83206-47-7

58-61-7

~15%

39007-51-7

Literature: Guengerich, F. Peter; Raney, Veronica M. Journal of the American Chemical Society, 1992 , vol. 114, # 3 p. 1074 - 1080

19263-02-6

58-61-7

~10%

91898-81-6

39007-51-7

Literature: Nair, Vasu; Offerman, Rick J.; Turner, Gregory A. Journal of Organic Chemistry, 1984 , vol. 49, # 21 p. 4021 - 4025

3536-89-8

39007-51-7

Literature: Inoue, Yasuo; Kuramochi, Takao; Sakurai, Michiharu; Tazawa, Ichiro Journal of the American Chemical Society, 1980 , vol. 102, # 17 p. 5574 - 5577

54285-77-7

38806-36-9

39007-51-7

Literature: Inoue, Yasuo; Kuramochi, Takao; Sakurai, Michiharu; Tazawa, Ichiro Journal of the American Chemical Society, 1980 , vol. 102, # 17 p. 5574 - 5577

2065-75-0

58-61-7

~5%

91898-81-6

39007-51-7

Literature: Kronberg, Leif; Asplund, Deanne; Maeki, Jukka; Sjoeholm, Rainer Chemical Research in Toxicology, 1996 , vol. 9, # 8 p. 1257 - 1263

107-20-0

58-61-7

~70%

39007-51-7

Literature: Patching, Simon G.; Baldwin, Stephen A.; Baldwin, Alexander D.; Young, James D.; Gallagher, Maurice P.; Henderson, Peter J. F.; Herbert, Richard B. Organic and Biomolecular Chemistry, 2005 , vol. 3, # 3 p. 462 - 470

58-61-7

17157-48-1

39007-51-7

Literature: Mikkola, Satu; Koissi, Niangoran; Ketomaeki, Kaisa; Rauvala, Susanna; Neuvonen, Kari; Loennberg, Harri European Journal of Organic Chemistry, 2000 , # 12 p. 2315 - 2323

58-61-7

50704-42-2

91898-81-6

39007-51-7

Literature: Mikkola, Satu; Koissi, Niangoran; Ketomaeki, Kaisa; Rauvala, Susanna; Neuvonen, Kari; Loennberg, Harri European Journal of Organic Chemistry, 2000 , # 12 p. 2315 - 2323

Precursor 8
83206-47-7 58-61-7 19263-02-6 3536-89-8
2065-75-0 107-20-0 17157-48-1 50704-42-2
DownStream 2
58-61-7 50663-83-7

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