1-METHYLADENOSINE CAS 15763-06-1

Introduction:Basic information about 1-METHYLADENOSINE CAS 15763-06-1, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

1-METHYLADENOSINE Basic information

Product Name:1-METHYLADENOSINE
Synonyms:N,6-Didehydro-1,6-dihydro-1-methyladenosine;1-METHYLADENOSINE;1-methyladenosine free base;(2R,3R,4R,5R)-2-(hydroxymethyl)-5-(6-imino-1-methyl-purin-9-yl)oxolane-3,4-diol;(2R,3R,4S,5R)-2-(6-Amino-1-methyl-1H-purin-9(2H)-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol;Adenosine, 1-methyl-;N1-Me-Adenosine;N1-Me-rA
CAS:15763-06-1
MF:C11H15N5O4
MW:281.27
EINECS:
Product Categories:Biochemicals and Reagents;Nucleoside Analogs;Nucleosides, Nucleotides, Oligonucleotides
Mol File:15763-06-1.mol

1-METHYLADENOSINE Chemical Properties

Melting point >217°C (dec.)
Boiling point 655.4±65.0 °C(Predicted)
density 1.88±0.1 g/cm3(Predicted)
storage temp. −20°C
solubility DMSO (Slightly), Water (Slightly, Sonicated)
pka13.24±0.70(Predicted)
form Solid
color White to Off-White
PH8.8
λmax258 (pH 2);258 (pH 7);259,260~265 (pH 13)
Stability:Hygroscopic, Light Sensitive
InChIInChI=1/C11H15N5O4/c1-15-3-14-10-6(9(15)12)13-4-16(10)11-8(19)7(18)5(2-17)20-11/h3-5,7-8,11-12,17-19H,2H2,1H3/t5-,7-,8-,11-/s3
InChIKeyGFYLSDSUCHVORB-ABFAXUGDNA-N
SMILESN1(C=NC2C(=N)N(C)C=NC1=2)[C@H]1[C@H](O)[C@H](O)[C@@H](CO)O1 |&1:11,12,14,16,r|

Safety Information

Safety Statements 24/25
WGK Germany WGK 3
HS Code 29389090
Storage Class11 - Combustible Solids

1-METHYLADENOSINE Usage And Synthesis

Description1-Methyladenosine is a modified nucleoside generated by the processing of tRNA by methyltransferases. The urinary excretion of 1-methyladenosine is elevated in several forms of cancer, supporting its use as a biomarker in early detection. It can also be monitored in serum. Urinary levels of 1-methyladenosine also increase during active rheumatoid arthritis.
Chemical PropertiesWhite to off-white crystalline powder
Uses1-Methyl Adenosine is a modified adenosine molecule created through the processing of tRNA by methyltransferases. The presence seen to be elevated in the urinary excretion of cancer patients. Thus it may be an early diagnosis biomarker.
DefinitionChEBI: A methyladenosine carrying a methyl substituent at position 1.
References[1] T. MUNNS H S. Methylation and processing of transfer ribonucleic acid in mammalian and bacterial cells.[J]. The Journal of Biological Chemistry, 1975, 4 1: 2143-2149. DOI: 10.1016/s0021-9258(19)41693-1
[2] VOLD B. Modified nucleosides of Bacillus subtilis transfer ribonucleic acids.[J]. Journal of Bacteriology, 1976, 127 1: 258-267. DOI: 10.1128/jb.127.1.258-267.1976
[3] TAKESHI CHUJO  Tsutomu S. Trmt61B is a methyltransferase responsible for 1-methyladenosine at position 58 of human mitochondrial tRNAs.[J]. RNA, 2012, 18 12: 2269-2276. DOI: 10.1261/rna.035600.112
[4] C. REYNAUD . Monitoring of urinary excretion of modified nucleosides in cancer patients using a set of six monoclonal antibodies[J]. Cancer letters, 1992, 61 3: Pages 255-262. DOI: 10.1016/0304-3835(92)90296-8
[5] A SEIDEL. Modified nucleosides: an accurate tumour marker for clinical diagnosis of cancer, early detection and therapy control[J]. British Journal of Cancer, 2006, 94 11: 1726-1733. DOI: 10.1038/sj.bjc.6603164
[6] WEI-YI HSU. Urinary nucleosides as biomarkers of breast, colon, lung, and gastric cancer in Taiwanese.[J]. PLoS ONE, 2013: e81701. DOI: 10.1371/journal.pone.0081701
[7] FENG CHEN. Identification of serum biomarkers of hepatocarcinoma through liquid chromatography/mass spectrometry-based metabonomic method[J]. Analytical and Bioanalytical Chemistry, 2011, 401 6. DOI: 10.1007/s00216-011-5245-3
[8] J G TEBIB. Relationship between urinary excretion of modified nucleosides and rheumatoid arthritis process.[J]. British journal of rheumatology, 1997, 36 9: 990-995. DOI: 10.1093/rheumatology/36.9.990

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