Basic Description

Synonyms	Cytidine 5'-(trihydrogen diphosphate) (9CI) \| Cytidine5'-(trihydrogendiphosphate) \| [(2R,3S,4R,5R)-5-(4-amino-2-oxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl phosphono hydrogen phosphate \| cytidine-diphosphate \| BRN 0063920 \| CDP Sodium Salt \| Cytidi
Specifications & Purity	≥98%
Storage Temp	Store at 2-8°C
Shipped In	Wet ice

Associated Targets(Human)

RRM1 Tclin Ribonucleoside-diphosphate reductase large subunit (0 Activities)

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Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

P2RY2 Tclin P2Y purinoceptor 2 (0 Activities)

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Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

P2RY6 Tchem P2Y purinoceptor 6 (0 Activities)

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Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

P2RY4 Tchem P2Y purinoceptor 4 (0 Activities)

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Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

P2RY6 Tchem Pyrimidinergic receptor P2Y6 (717 Activities)

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

P2RY4 Tchem Pyrimidinergic receptor P2Y4 (598 Activities)

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P2RY2 Tclin Purinergic receptor P2Y2 (1109 Activities)

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RRM1 Tclin Ribonucleoside-diphosphate reductase RR1 (391 Activities)

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Mechanisms of Action

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

Names and Identifiers

IUPAC Name	[(2R,3S,4R,5R)-5-(4-amino-2-oxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl phosphono hydrogen phosphate
INCHI	InChI=1S/C9H15N3O11P2/c10-5-1-2-12(9(15)11-5)8-7(14)6(13)4(22-8)3-21-25(19,20)23-24(16,17)18/h1-2,4,6-8,13-14H,3H2,(H,19,20)(H2,10,11,15)(H2,16,17,18)/t4-,6-,7-,8-/m1/s1
InChi Key	ZWIADYZPOWUWEW-XVFCMESISA-N
Canonical SMILES	C1=CN(C(=O)N=C1N)C2C(C(C(O2)COP(=O)(O)OP(=O)(O)O)O)O
Isomeric SMILES	C1=CN(C(=O)N=C1N)[C@H]2[C@@H]([C@@H]([C@H](O2)COP(=O)(O)OP(=O)(O)O)O)O
PubChem CID	6132
Molecular Weight	403.18

Certificates

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Citations of This Product

How to Cite Aladdin Scientific Products?

1. Lai Liang, Zhang Mengyun, Liu Chusheng, Qu Jiahuan, Xu Dongsheng, Jiang Zhengjin. (2023) A comprehensive evaluation of a polymeric zwitterionic hydrophilic monolith for nucleotide separation. ANALYTICAL SCIENCES, (1-7). [PMID:37843729] [10.1007/s44211-023-00430-5]
2. Mingyu Zhang, Yuqi Tang, Rui Xu, Dong Yan, Shuangping Xu, Yanqing Qu, Jingyu Xu, Hongge Jia. (2023) Synthesis of a novel phosphate-containing ligand rhodium catalyst and exploration of its optimal reaction conditions and mechanism for the polymerization of phenylacetylene. HETEROCYCLIC COMMUNICATIONS, 29 (1): [PMID:9169142] [10.1515/hc-2022-0163]
3. Yuqin Wang, Pingping Fan, Shanyu Zhang, Liying Wang, Xinyue Li, Wendong Jia, Yao Liu, Kefan Wang, Xiaoyu Du, Panke Zhang, Shuo Huang. (2022) Discrimination of Ribonucleoside Mono-, Di-, and Triphosphates Using an Engineered Nanopore. ACS Nano, 16 (12): (21356–21365). [PMID:36475606] [10.1021/acsnano.2c09662]

References

1. Lai Liang, Zhang Mengyun, Liu Chusheng, Qu Jiahuan, Xu Dongsheng, Jiang Zhengjin. (2023) A comprehensive evaluation of a polymeric zwitterionic hydrophilic monolith for nucleotide separation. ANALYTICAL SCIENCES, (1-7). [PMID:37843729] [10.1007/s44211-023-00430-5]
2. Mingyu Zhang, Yuqi Tang, Rui Xu, Dong Yan, Shuangping Xu, Yanqing Qu, Jingyu Xu, Hongge Jia. (2023) Synthesis of a novel phosphate-containing ligand rhodium catalyst and exploration of its optimal reaction conditions and mechanism for the polymerization of phenylacetylene. HETEROCYCLIC COMMUNICATIONS, 29 (1): [PMID:9169142] [10.1515/hc-2022-0163]
3. Yuqin Wang, Pingping Fan, Shanyu Zhang, Liying Wang, Xinyue Li, Wendong Jia, Yao Liu, Kefan Wang, Xiaoyu Du, Panke Zhang, Shuo Huang. (2022) Discrimination of Ribonucleoside Mono-, Di-, and Triphosphates Using an Engineered Nanopore. ACS Nano, 16 (12): (21356–21365). [PMID:36475606] [10.1021/acsnano.2c09662]

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Cytidine-5′-diphosphate - 98%, high purity , CAS No.63-38-7