JavaScript seems to be disabled in your browser. For the best experience on our site, be sure to turn on Javascript in your browser.

This is a demo store. No orders will be fulfilled.

Account

Settings

Language

྾

Home
Chemistry & Biochemicals
Chemical Synthesis
Coupling Reagents
2′-Deoxyguanosine hydrate - 99%, high purity , CAS No.207121-55-9

Skip to the end of the images gallery

Skip to the beginning of the images gallery

2′-Deoxyguanosine hydrate - 99%, high purity , CAS No.207121-55-9

2 Citations

COA

Grade & Purity:

≥99%

Cas Number: 207121-55-9
Molecular Weight: 267.24 (anhydrous basis)
MDL number: MFCD00150760
PubChem CID: 135445705
PubChem SID: 488202913

In stock

Item Number

D168464

Grouped product items
SKU	Size	Availability	Price
D168464-100mg	100mg	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$73.90
D168464-5g	5g	4	$997.90
D168464-25g	25g	4	$3,434.90

Basic Description

Synonyms	LZSCQUCOIRGCEJ-FPKZOZHISA-N \| 2`-Deoxyguanosine monohydrate \| 2'deoxyguanosine monohydrate \| 2'-Deoxyguanosine monohydrate \| 2'-deoxyguanosine mono-hydrate \| 2-Deoxyguanosine monohydrate \| 2-Amino-9-((2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2
Specifications & Purity	≥99%
Storage Temp	Room temperature
Shipped In	Normal

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Nucleosides, nucleotides, and analogues
  - Class Purine nucleosides
    - Subclass Purine 2'-deoxyribonucleosides

Kingdom	Organic compounds
Superclass	Nucleosides, nucleotides, and analogues
Class	Purine nucleosides
Subclass	Purine 2'-deoxyribonucleosides
Intermediate Tree Nodes	Not available
Direct Parent	Purine 2'-deoxyribonucleosides
Alternative Parents	Hypoxanthines Hydroxypyrimidines Aminopyrimidines and derivatives N-substituted imidazoles Oxolanes Heteroaromatic compounds Secondary alcohols Oxacyclic compounds Azacyclic compounds Primary amines Primary alcohols Organic oxides Hydrocarbon derivatives
Molecular Framework	Aromatic heteropolycyclic compounds
Substituents	Purine 2'-deoxyribonucleoside - Hypoxanthine - Imidazopyrimidine - Purine - Aminopyrimidine - Hydroxypyrimidine - N-substituted imidazole - Pyrimidine - Azole - Imidazole - Heteroaromatic compound - Oxolane - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Organooxygen compound - Organonitrogen compound - Amine - Alcohol - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Primary alcohol - Primary amine - Aromatic heteropolycyclic compound
Description	This compound belongs to the class of organic compounds known as purine 2'-deoxyribonucleosides. These are compounds consisting of a purine linked to a ribose which lacks a hydroxyl group at position 2.
External Descriptors	Not available
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. DOI: 10.1186/s13321-016-0174-y

Associated Targets(Human)

TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)

Discover Target: TDP1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ERG Tbio Transcriptional regulator ERG (5589 Activities)

Discover Target: ERG

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

GMNN Tbio Geminin (128009 Activities)

Discover Target: GMNN

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ATAD5 Tbio ATPase family AAA domain-containing protein 5 (122566 Activities)

Discover Target: ATAD5

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

Pubchem Sid	488202913
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488202913
IUPAC Name	2-amino-9-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-1H-purin-6-one;hydrate
INCHI	InChI=1S/C10H13N5O4.H2O/c11-10-13-8-7(9(18)14-10)12-3-15(8)6-1-4(17)5(2-16)19-6;/h3-6,16-17H,1-2H2,(H3,11,13,14,18);1H2/t4-,5+,6+;/m0./s1
InChIKey	LZSCQUCOIRGCEJ-FPKZOZHISA-N
Smiles	C1C(C(OC1N2C=NC3=C2N=C(NC3=O)N)CO)O.O
Isomeric SMILES	C1[C@@H]([C@H](O[C@H]1N2C=NC3=C2N=C(NC3=O)N)CO)O.O
WGK Germany	3
PubChem CID	135445705
Molecular Weight	267.24 (anhydrous basis)

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

8 results found

Lot Number	Certificate Type	Date	Item
L2215325	Certificate of Analysis	Sep 11, 2024	D168464
L2215431	Certificate of Analysis	Sep 11, 2024	D168464
L2215355	Certificate of Analysis	Sep 11, 2024	D168464
C1905064	Certificate of Analysis	Jul 08, 2024	D168464
F2221358	Certificate of Analysis	Apr 03, 2024	D168464
F2221360	Certificate of Analysis	Apr 03, 2024	D168464
F2221359	Certificate of Analysis	May 25, 2022	D168464
F2221361	Certificate of Analysis	May 25, 2022	D168464

Chemical and Physical Properties

Specific Rotation[α]	[α]20/D −30°, c = 0.2 in H2O
Melt Point(°C)	>300 °C (dec.) (lit.)
Molecular Weight	285.260 g/mol
XLogP3
Hydrogen Bond Donor Count	5
Hydrogen Bond Acceptor Count	7
Rotatable Bond Count	2
Exact Mass	285.107 Da
Monoisotopic Mass	285.107 Da
Topological Polar Surface Area	136.000 Å²
Heavy Atom Count	20
Formal Charge	0
Complexity	417.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	3
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	2

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Ji-shuo Chang, Zhong-xiao Lin, Ya-juan Liu, Si-ming Yang, Yu Zhang, Xi-yong Yu. (2021) Ultra performance liquid chromatography–tandem mass spectrometry assay for the quantification of RNA and DNA methylation. JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 197 (113969).
2. Mengzhen Jiang, Ruohan Xu, Chunyan Yang, Haili Wang, Jinyuan Cai, Yanrong Wen, Mingfu Ye, Tingxuan Yan, Shuangshou Wang. (2025) Boronate affinity-mediated multi-mode visual sensing of cis-diol compounds in both biological and food samples. SENSORS AND ACTUATORS B-CHEMICAL, (137335).

Solution Calculators

Molarity Calculator

Determine the necessary mass, volume, or concentration for preparing a solution.

Mass

Concentration

Volume

M. Wt*

g/mol

*When preparing stock solutions, always use the batch-specific molecular weight of the product found on the vial label and the Certificate of Analysis (available online).

Dilution Calculator

Determine the dilution needed to prepare a stock solution.

Concentration 1 (C1)

Volume 1 (V1)

Concentration 2 (C2)

Volume 2 (V2)

Reconstitution Calculator

The reconstitution calculator enables you to quickly determine the volume of a reagent needed to reconstitute your vial. Just enter the mass of the reagent and the target concentration, and the calculator will do the rest.

Volume (to add to vial)

Mass (in vial)

Desired Reconstitution Concentration

Reviews

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.