Nucleotides

2'-Modified Nucleotides
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3'-Modified Nucleotides
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Arabinonucleotides
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Dinucleosides Phosphate
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Fluorescent Nucleotides
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Halogen Nucleotides
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Phosphate Modified Nucleotides (93/93) Ribonucleotides
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5-Fluoro-UMP

Description: 5-Fluoro-UMP, a potent antineoplastic nucleotide analog, is utilized to combat several forms of cancer. It thwarts the synthesis of RNA and DNA by disturbing their natural cellular processes, ultimately culminating in apoptosis. Moreover, it's a key research tool to assess how changes in nucleotide metabolism can impact cellular maturation and proliferation.
CAT: BRP-01839
CAS: 796-66-7
MF: C9H12FN2O9P
MF: 342.17
Purity: ≥97% by HPLC
Appearance: clear aqueous solution
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Density: 1.93±0.1 g/cm3
InChIKey: RNBMPPYRHNWTMA-UAKXSSHOSA-N
CanonicalSMILES: C1=C(C(=O)NC(=O)N1C2C(C(C(O2)COP(=O)(O)O)O)O)F
IUPAC Name: [(2R,3S,4R,5R)-5-(5-fluoro-2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl dihydrogen phosphate
InChI: InChI=1S/C9H12FN2O9P/c10-3-1-12(9(16)11-7(3)15)8-6(14)5(13)4(21-8)2-20-22(17,18)19/h1,4-6,8,13-14H,2H2,(H,11,15,16)(H2,17,18,19)/t4-,5-,6-,8-/m1/s1
Synonyms: 5F-UMP; 5-Fluorouridine-monophosphate; Fosfluoridine; 5-Fluorouridylic acid; 5-fluorouridine 5'-(dihydrogen phosphate); 5-Fluoro-4-hydroxy-1-(5-O-phosphonopentofuranosyl)pyrimidin-2(1H)-one; ((2R,3S,4R,5R)-5-(5-Fluoro-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl dihydrogen phosphate; 5-Fluoro-5'-uridylic acid; Uridine, 5-fluoro-, 5'-(dihydrogen phosphate); Uridine, 5-fluoro-, 5'-phosphate; 5-Fluorouridine 5'-monophosphate; 5-Fluorouridine 5'-phosphate; 5-Fluorouridine monophosphate; 5-Fluorouridylic acid
Related CAS: 99631-71-7 (diammonia salt) ; 374083-83-7 (x-ammonium salt) ; 67550-10-1 (disodium salt)

5-Fluorouridine-5'-monophosphate sodium salt

Description: 5-fluorouridine 5'-monophosphate is a pyrimidine ribonucleoside 5'-monophosphate having 5-fluorouracil as the pyrimidine component. It has a role as a drug metabolite. It is a pyrimidine ribonucleoside 5'-monophosphate and an organofluorine compound. It derives from a uridine 5'-monophosphate.
CAT: BRP-01840
CAS: 67550-10-1
MF: C9H10FN2Na2O9P
MF: 386.14
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InChIKey: MPRJYKKHPJYUND-HGXRYYEQSA-L
CanonicalSMILES: [Na].[Na].O=C1NC(=O)N(C=C1F)C2OC(COP(=O)(O)O)C(O)C2O
IUPAC Name: disodium;((2R,3S,4R,5R)-5-(5-fluoro-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl phosphate
InChI: InChI=1S/C9H12FN2O9P.2Na/c10-3-1-12(9(16)11-7(3)15)8-6(14)5(13)4(21-8)2-20-22(17,18)19;;/h1,4-6,8,13-14H,2H2,(H,11,15,16)(H2,17,18,19);;/q;2*+1/p-2/t4-,5-,6-,8-;;/m1../s1
Synonyms: 5'-Uridylic acid, 5-fluoro-, disodium salt; 5F-UMP disodium salt; 5-Fluoro-5'-uridylic acid disodium salt; 5-Fluorouridine 5'-monophosphate disodium salt; 5-Fluorouridine 5'-phosphate disodium salt; 5-Fluorouridine monophosphate disodium salt; 5-Fluorouridylic acid disodium salt; 5-fluorouridine 5'-(dihydrogen phosphate) disodium salt; 5-Fluoro-UMP disodium salt
Related CAS: 796-66-7 (free acid)

5-Fluorouridine-5'-diphosphate

Description: 5-Fluorouridine-5'-diphosphate, a pivotal biomedicine entity, demonstrates profound significance in diverse ailments, particularly cancer. Operating as an efficient anticancer intervention, this derivative effectively impedes the expansion and reproduction of malignant cells. Its mechanism involves interrupting DNA synthesis, thereby facilitating the control over specific cancer variants.
CAT: BRP-01841
CAS: 803-98-5
MF: C9H13FN2O12P2
MF: 422.15
Purity: ≥97% by HPLC
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Density: 2.04±0.1 g/cm3
InChIKey: FOZCNVFQOJRHFF-UAKXSSHOSA-N
CanonicalSMILES: C1=C(C(=O)NC(=O)N1C2C(C(C(O2)COP(=O)(O)OP(=O)(O)O)O)O)F
IUPAC Name: [(2R,3S,4R,5R)-5-(5-fluoro-2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl phosphono hydrogen phosphate
InChI: InChI=1S/C9H13FN2O12P2/c10-3-1-12(9(16)11-7(3)15)8-6(14)5(13)4(23-8)2-22-26(20,21)24-25(17,18)19/h1,4-6,8,13-14H,2H2,(H,20,21)(H,11,15,16)(H2,17,18,19)/t4-,5-,6-,8-/m1/s1
Synonyms: 5-Fluorouridine 5'-(trihydrogen diphosphate); Uridine, 5-fluoro-, 5'-(trihydrogen pyrophosphate); Uridine, 5-fluoro-, 5'-pyrophosphate; 5-Fluoro-UDP; 5-Fluorouridine 5'-diphosphate; 5-Fluorouridine diphosphate; 5-F-UDP
Related CAS: 980-18-7 (trilithium salt)

5-Fluorouridine-diphosphate disodium salt

Description: 5-Fluorouridine-diphosphate disodium salt, a potent biochemical, holds great promise in treating cancer. Its dual mechanism of RNA synthesis inhibition and nucleotide metabolism inhibition leads to its effectiveness in minimizing tumor growth. Remarkably, it has been proven to specifically target breast, colon, and pancreatic cancers. Clinical insights indicate that it is applied in combination chemotherapy to achieve maximum efficacy.
CAT: BRP-01842
MF: C9H11FN2Na2O12P2
MF: 466.11
Purity: ≥97% by HPLC
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InChIKey: AHYBVRBYXCFNSY-HGXRYYEQSA-L
CanonicalSMILES: [Na].[Na].O=C1NC(=O)N(C=C1F)C2OC(COP(=O)(O)OP(=O)(O)O)C(O)C2O
IUPAC Name: disodium;((2R,3S,4R,5R)-5-(5-fluoro-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl hydrogen diphosphate
InChI: InChI=1S/C9H13FN2O12P2.2Na/c10-3-1-12(9(16)11-7(3)15)8-6(14)5(13)4(23-8)2-22-26(20,21)24-25(17,18)19;;/h1,4-6,8,13-14H,2H2,(H,20,21)(H,11,15,16)(H2,17,18,19);;/q;2*+1/p-2/t4-,5-,6-,8-;;/m1../s1
Synonyms: 5-Fluorouridine 5'-(trihydrogen diphosphate) disodium salt; 5-Fluoro-UDP disodium salt; 5-Fluorouridine diphosphate disodium salt; Uridine, 5-fluoro-, 5'-(trihydrogen pyrophosphate), disodium salt; Uridine, 5-fluoro-, 5'-pyrophosphate, disodium salt; 5-F-UDP disodium salt; 5-Fluorouridine 5'-diphosphate disodium salt
Related CAS: 803-98-5 (free acid)

3'-O-TBDMS-2'-O-methyl-Uridine-5'-triphosphate

Description: 3'-O-TBDMS-2'-O-methyl-Uridine-5'-triphosphate, a synthetic nucleotide analogue, is a versatile and dynamic molecule that has found extensive use within biomedical research. With numerous applications available, this molecule has been shown to successfully penetrate cellular pathways linked to RNA and DNA function, ultimately leading to cancer and viral infection treatment by limiting nucleotide synthesis, and hence thwarting virus and cancer cell replication. Such therapeutic potential, coupled with its characteristic specificity and otherwise low toxicity, make this molecule a prime candidate for exploring advanced horizons within the field of biomedicine.
CAT: BRP-01843
MF: C16H31N2O15P3Si
MF: 612.43
Purity: ≥97% by HPLC
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InChIKey: YNWBJRPNEDBXTK-FMKGYKFTSA-N
IUPAC Name: ((2R,3R,4R,5R)-3-((tert-butyldimethylsilyl)oxy)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-4-methoxytetrahydrofuran-2-yl)methyl tetrahydrogen triphosphate
InChI: InChI=1S/C16H31N2O15P3Si/c1-16(2,3)37(5,6)31-12-10(9-29-35(24,25)33-36(26,27)32-34(21,22)23)30-14(13(12)28-4)18-8-7-11(19)17-15(18)20/h7-8,10,12-14H,9H2,1-6H3,(H,24,25)(H,26,27)(H,17,19,20)(H2,21,22,23)/t10-,12-,13-,14-/m1/s1
Synonyms: (((2R,3R,4R,5R)-3-((tert-butyldimethylsilyl)oxy)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-4-methoxytetrahydrofuran-2-yl)methyl)triphosphoric acid; 3'-O-TBDMS-2'-O-Me-UTP; 3'-O-TBDMS-2'-OMe-UTP

2'-O-Methyladenosine-5'-triphosphate trisodium salt

Description: 2'-O-Methyladenosine-5'-triphosphate trisodium salt is a powerful tool widely used in the biomedical industry. With its ability to serve as a substrate for various enzymatic reactions, it plays a vital role in research related to mRNA modification and RNA processing. It is particularly valuable for investigating the roles of 2'-O-methyladenosine in RNA structure and function.
CAT: BRP-01844
MF: C11H15N5Na3O13P3
MF: 587.15
Purity: ≥97% by HPLC
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Storage: Store at -20°C
InChIKey: FBSPORIDBYRWCL-MTQUBGKESA-K
Solubility: Soluble in Water
CanonicalSMILES: COC1C(C(OC1N2C=NC3=C(N=CN=C32)N)COP(=O)([O-])OP(=O)([O-])OP(=O)(O)[O-])O.[Na+].[Na+].[Na+]
IUPAC Name: trisodium;[[[(2R,3R,4R,5R)-5-(6-aminopurin-9-yl)-3-hydroxy-4-methoxyoxolan-2-yl]methoxy-oxidophosphoryl]oxy-oxidophosphoryl] hydrogen phosphate
InChI: InChI=1S/C11H18N5O13P3.3Na/c1-25-8-7(17)5(2-26-31(21,22)29-32(23,24)28-30(18,19)20)27-11(8)16-4-15-6-9(12)13-3-14-10(6)16;;;/h3-5,7-8,11,17H,2H2,1H3,(H,21,22)(H,23,24)(H2,12,13,14)(H2,18,19,20);;;/q;3*+1/p-3/t5-,7-,8-,11-;;;/m1.../s1
Synonyms: 2'-O-methyl-Adenosine-5'-triphosphate, trisodium salt; trisodium ((2R,3R,4R,5R)-5-(6-amino-9H-purin-9-yl)-3-hydroxy-4-methoxytetrahydrofuran-2-yl)methyl hydrogen triphosphate; 2'-O-Me-ATP trisodium salt; Trisodium 5'-O-[({[(hydroxyphosphinato)oxy]phosphinato}oxy)phosphinato]-2'-O-methyladenosine; Adenosine, 2'-O-methyl-, 5'-(tetrahydrogen triphosphate), sodium salt (1:3); 2'-O-Methyladenosine 5'-(tetrahydrogen triphosphate) trisodium salt; 2'-O-Methyl-ATP trisodium salt
Related CAS: 30948-06-2 (free acid) ; 100020-58-4 (tetrasodium salt)

Adenosine N-phosphate 5'-phosphosulfate lithium salt

Description: Adenosine N-phosphate 5'-phosphosulfate lithium salt is an indispensable compound prevalent in the biomedical field, exhibiting its significant relevance in the research and development of sulfated glycosaminoglycans, integral constituents of connective tissues. Additionally, it serves as an appreciable substrate for enzymes participating in compound metabolism and detoxification mechanisms.
CAT: BRP-01873
CAS: 109434-21-1
MF: C10H15N5O13P2S.xLi
MF: 507.26 (free acid)
Purity: ≥98%
Appearance: Clear colorless Liquid
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Storage: Store at -20 °C, Always avoid freeze-thaw cycles
IUPAC Name: lithium;[[9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-[[hydroxy(sulfooxy)phosphoryl]oxymethyl]oxolan-2-yl]purin-6-yl]amino]phosphonic acid
Synonyms: Sulfuric acid, 5'-anhydride with N-phosphono-5'-adenylic acid, lithium salt (1:x); Sulfuric acid, 5'-anhydride with N-phosphono-5'-adenylic acid, lithium salt; N-Phosphoadenosine-5'-phosphosulfate lithium salt
Related CAS: 765231-59-2 (free acid)

Adenosine 3'-phosphate 5'-phosphosulfate

Description: Adenosine 3'-phosphate 5'-phosphosulfate is a pivotal compound extensively employed in the biomedical sector, exhibiting properties as a crucial coenzyme implicated in sulfate activation. Its multifaceted functionality includes facilitating the research and development of sulfate esters and orchestrating the regulation of numerous intricate biological processes.
CAT: BRP-01874
CAS: 482-67-7
MF: C10H15N5O13P2S
MF: 507.27
Purity: ≥95%
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Storage: Store at -20 °C, Always avoid freeze-thaw cycles
Density: 2.56±0.1 g/cm3
InChIKey: GACDQMDRPRGCTN-KQYNXXCUSA-N
CanonicalSMILES: C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)COP(=O)(O)OS(=O)(=O)O)OP(=O)(O)O)O)N
IUPAC Name: [(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-3-phosphonooxyoxolan-2-yl]methyl sulfo hydrogen phosphate
InChI: InChI=1S/C10H15N5O13P2S/c11-8-5-9(13-2-12-8)15(3-14-5)10-6(16)7(27-29(17,18)19)4(26-10)1-25-30(20,21)28-31(22,23)24/h2-4,6-7,10,16H,1H2,(H,20,21)(H2,11,12,13)(H2,17,18,19)(H,22,23,24)/t4-,6-,7-,10-/m1/s1
Synonyms: Phosphoadenosine phosphosulfate; 3'-Phosphoadenylyl sulfate; PAPS; 3'-Adenylic acid, 5'-(dihydrogen phosphate), 5'-anhydride with sulfuric acid; Adenosine 3',5'-diphosphate, 5'-anhydride with sulfuric acid; Adenosine, 3',5'-bis(dihydrogen phosphate), 5'-monoanhydride with sulfuric acid; 3'-Phosphoadenosine 5'-phosphosulfate; 5'-Adenylyl sulfate 3'-phosphate; Adenosine 3'-phosphate 5'-sulfatophosphate; Adenosine 5'-phosphosulfate 3'-phosphate; PAPS (nucleotide)
Related CAS: 1374115-02-2 (tetrasodium salt) ; 102029-54-9 (tetralithium salt)

Adenosine 3'-Phosphate 5'-Phosphosulfate Tetralithium Salt

Description: Adenosine 3'-Phosphate 5'-Phosphosulfate Tetralithium Salt is a pivotal compound recompound, playing an indispensable role in elucidating the intricate intricacies of adenosine nucleotide metabolism and signaling pathways. It functions as a substrate for the esteemed enzyme APS kinase, thereby exerting its influence on the research and development of both phosphoadenosine phosphosulfate (PAPS) and ATP.
CAT: BRP-01875
CAS: 102029-54-9
MF: C10H11Li4N5O13P2S
MF: 531.00
Purity: ≥80%
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Storage: Store at -20 °C, Always avoid freeze-thaw cycles
InChIKey: XWIJNPMPIUNGDA-KWIZKVQNSA-J
Solubility: Soluble in Water
CanonicalSMILES: [Li+].[Li+].[Li+].[Li+].C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)COS(=O)(=O)OP(=O)([O-])[O-])OP(=O)([O-])[O-])O)N
IUPAC Name: tetralithium;[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-3-phosphonatooxyoxolan-2-yl]methoxysulfonyl phosphate
InChI: InChI=1S/C10H15N5O13P2S.4Li/c11-8-5-9(13-2-12-8)15(3-14-5)10-6(16)7(27-29(17,18)19)4(26-10)1-25-31(23,24)28-30(20,21)22;;;;/h2-4,6-7,10,16H,1H2,(H2,11,12,13)(H2,17,18,19)(H2,20,21,22);;;;/q;4*+1/p-4/t4-,6-,7-,10-;;;;/m1..../s1
Synonyms: Adenosine 3'-phosphate 5'-phosphosulfate lithium salt; Phosphoadenosine phosphosulfate tetralithium salt; 3'-Phosphoadenylyl sulfate tetralithium salt; PAPS tetralithium salt; 3'-Phosphoadenosine 5'-phosphosulfate tetralithium salt; 5'-Adenylyl sulfate 3'-phosphate tetralithium salt; Adenosine 3'-phosphate 5'-sulfatophosphate tetralithium salt; Adenosine 5'-phosphosulfate 3'-phosphate tetralithium salt
Related CAS: 482-67-7 (free acid)

Adenosine 2'-phosphate 5'-phosphosulfate

Description: Adenosine 2'-phosphate 5'-phosphosulfate (PAPS) is an essential molecule in biochemistry, acting as a universal sulfate donor in numerous sulfation reactions. Its role in metabolism, detoxification, and physiological regulation underscores its significance in both health and disease.
CAT: BRP-01876
CAS: 62230-89-1
MF: C10H15N5O13P2S
MF: 507.27
Purity: ≥95%
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Storage: Store at -20 °C, Always avoid freeze-thaw cycles
Density: 2.56±0.1 g/cm3
InChIKey: SGNZKKOMSOPYFR-KQYNXXCUSA-N
CanonicalSMILES: C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)COP(=O)(O)OS(=O)(=O)O)O)OP(=O)(O)O)N
IUPAC Name: [(2R,3R,4R,5R)-5-(6-aminopurin-9-yl)-3-hydroxy-4-phosphonooxyoxolan-2-yl]methyl sulfo hydrogen phosphate
InChI: InChI=1S/C10H15N5O13P2S/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(27-29(17,18)19)6(16)4(26-10)1-25-30(20,21)28-31(22,23)24/h2-4,6-7,10,16H,1H2,(H,20,21)(H2,11,12,13)(H2,17,18,19)(H,22,23,24)/t4-,6-,7-,10-/m1/s1
Synonyms: 2'-Adenylic acid, 5'-(dihydrogen phosphate), 5'-anhydride with sulfuric acid; 2'-Phosphoadenosine 5'-phosphosulfate; iso-PAPS; IsoPAPS

Adenosine 3'-phosphate 5'-phosphosulfate, N-ethylethanamine

Description: Adenosine 3'-phosphate 5'-phosphosulfate, N-ethylethanamine is a modified nucleotide where adenosine is doubly phosphorylated at the 3' and 5' positions, with a sulfate group attached to the 5' phosphate. This compound is significant in biochemical studies for understanding nucleotide modifications and their roles in cellular processes.
CAT: BRP-01877
CAS: 936827-85-9
MF: C10H15N5O13P2S.xC4H11N
MF: 507.27 (free base)
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Storage: Store at -20 °C, Always avoid freeze-thaw cycles
IUPAC Name: [(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-3-phosphonooxyoxolan-2-yl]methyl sulfo hydrogen phosphate;N-ethylethanamine
Synonyms: 3'-Adenylic acid, 5'-(dihydrogen phosphate), 5'-anhydride with sulfuric acid, compd. with N-ethylethanamine (1:x); Phosphoadenosine phosphosulfate, N-ethylethanamine; 3'-Phosphoadenylyl sulfate, N-ethylethanamine; PAPS, N-ethylethanamine; 3'-Phosphoadenosine 5'-phosphosulfate, N-ethylethanamine; 5'-Adenylyl sulfate 3'-phosphate, N-ethylethanamine; Adenosine 3'-phosphate 5'-sulfatophosphate, N-ethylethanamine; Adenosine 5'-phosphosulfate 3'-phosphate, N-ethylethanamine
Related CAS: 482-67-7 (free base)

Adenosine 3'-phosphate 5'-phosphosulfate, piperidine

Description: Adenosine 3'-phosphate 5'-phosphosulfate, piperidine is a chemically modified nucleotide where adenosine is phosphorylated at both the 3' and 5' positions, with a sulfate group attached to the 5' phosphate. This compound is used in biochemical research to study the roles of nucleotide modifications in various cellular processes and signaling pathways.
CAT: BRP-01878
CAS: 936827-86-0
MF: C10H15N5O13P2S.xC5H11N
MF: 507.27 (free base)
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Storage: Store at -20 °C, Always avoid freeze-thaw cycles
IUPAC Name: [(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-3-phosphonooxyoxolan-2-yl]methyl sulfo hydrogen phosphate;piperidine
Synonyms: 3'-Adenylic acid, 5'-(dihydrogen phosphate), 5'-anhydride with sulfuric acid, compd. with piperidine (1:x); Phosphoadenosine phosphosulfate, piperidine; 3'-Phosphoadenylyl sulfate, piperidine; PAPS, piperidine; 3'-Phosphoadenosine 5'-phosphosulfate, piperidine; 5'-Adenylyl sulfate 3'-phosphate, piperidine; Adenosine 3'-phosphate 5'-sulfatophosphate, piperidine; Adenosine 5'-phosphosulfate 3'-phosphate, piperidine
Related CAS: 482-67-7 (free base)

Adenosine 3'-phosphate 5'-phosphosulfate, Triethanolamine

Description: Adenosine 3'-phosphate 5'-phosphosulfate, triethanolamine is a modified nucleotide where adenosine is phosphorylated at both the 3' and 5' positions, with a sulfate group attached to the 5' phosphate. This compound is significant in biochemical research for investigating the roles of nucleotide modifications in cellular metabolism and signaling pathways.
CAT: BRP-01879
CAS: 936827-88-2
MF: C10H15N5O13P2S.xC6H15NO3
MF: 507.27 (free base)
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IUPAC Name: [(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-3-phosphonooxyoxolan-2-yl]methyl sulfo hydrogen phosphate;2-[bis(2-hydroxyethyl)amino]ethanol
Synonyms: 3'-Adenylic acid, 5'-(dihydrogen phosphate), 5'-anhydride with sulfuric acid, compd. with 2,2',2''-nitrilotris[ethanol] (1:x); Phosphoadenosine phosphosulfate, Triethanolamine; 3'-Phosphoadenylyl sulfate, Triethanolamine; PAPS, Triethanolamine; 3'-Phosphoadenosine 5'-phosphosulfate, Triethanolamine; 5'-Adenylyl sulfate 3'-phosphate, Triethanolamine; Adenosine 3'-phosphate 5'-sulfatophosphate, Triethanolamine; Adenosine 5'-phosphosulfate 3'-phosphate, Triethanolamine
Related CAS: 482-67-7 (free base)

Adenosine 3'-phosphate 5'-phosphosulfate, N,N-dimethylmethanamine

Description: Adenosine 3'-phosphate 5'-phosphosulfate, N,N-dimethylmethanamine is a modified nucleotide where adenosine is phosphorylated at both the 3' and 5' positions, with a sulfate group attached to the 5' phosphate. This compound is used in biochemical research to investigate the roles of nucleotide modifications in various cellular processes, including sulfation pathways and metabolic reactions.
CAT: BRP-01880
CAS: 936827-90-6
MF: C10H15N5O13P2S.xC3H9N
MF: 507.27 (free base)
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Storage: Store at -20 °C, Always avoid freeze-thaw cycles
IUPAC Name: [(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-3-phosphonooxyoxolan-2-yl]methyl sulfo hydrogen phosphate;N,N-dimethylmethanamine
Synonyms: 3'-Adenylic acid, 5'-(dihydrogen phosphate), 5'-anhydride with sulfuric acid, compd. with N,N-dimethylmethanamine (1:x); Phosphoadenosine phosphosulfate, N,N-dimethylmethanamine; 3'-Phosphoadenylyl sulfate, N,N-dimethylmethanamine; PAPS, N,N-dimethylmethanamine; 3'-Phosphoadenosine 5'-phosphosulfate, N,N-dimethylmethanamine; 5'-Adenylyl sulfate 3'-phosphate, N,N-dimethylmethanamine; Adenosine 3'-phosphate 5'-sulfatophosphate, N,N-dimethylmethanamine; Adenosine 5'-phosphosulfate 3'-phosphate, N,N-dimethylmethanamine
Related CAS: 482-67-7 (free base)

Adenosine 3'-phosphate 5'-phosphosulfate, aziridine homopolymer

Description: Adenosine 3'-phosphate 5'-phosphosulfate, aziridine homopolymer is a complex biochemical compound where adenosine is doubly phosphorylated at the 3' and 5' positions, with a sulfate group attached to the 5' phosphate, and conjugated to an aziridine homopolymer. Adenosine 3'-phosphate 5'-phosphosulfate, aziridine homopolymer is an advanced biochemical tool used to study and manipulate sulfation processes in cellular metabolism and pharmacology. Its unique combination of PAPS and aziridine homopolymer offers enhanced properties for research and potential therapeutic applications.
CAT: BRP-01881
CAS: 936827-92-8
MF: C10H15N5O13P2S.x(C2H5N)x
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Storage: Store at -20 °C, Always avoid freeze-thaw cycles
IUPAC Name: [(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-3-phosphonooxyoxolan-2-yl]methyl sulfo hydrogen phosphate;aziridine
Synonyms: 3'-Adenylic acid, 5'-(dihydrogen phosphate), 5'-anhydride with sulfuric acid, compd. with aziridine homopolymer; Phosphoadenosine phosphosulfate, aziridine homopolymer; 3'-Phosphoadenylyl sulfate, aziridine homopolymer; PAPS, aziridine homopolymer; 3'-Phosphoadenosine 5'-phosphosulfate, aziridine homopolymer; 5'-Adenylyl sulfate 3'-phosphate, aziridine homopolymer; Adenosine 3'-phosphate 5'-sulfatophosphate, aziridine homopolymer; Adenosine 5'-phosphosulfate 3'-phosphate, aziridine homopolymer
Related CAS: 482-67-7 (free base)

Adenosine 3'-phosphate 5'-phosphosulfate, butandiamine

Description: Adenosine 3'-phosphate 5'-phosphosulfate, butandiamine is a modified nucleotide where adenosine is phosphorylated at both the 3' and 5' positions, with a sulfate group attached to the 5' phosphate. Adenosine 3'-phosphate 5'-phosphosulfate, butandiamine is a specialized biochemical compound combining the sulfate-donating capabilities of PAPS with the unique properties imparted by butandiamine. This makes it a valuable tool for studying sulfation processes, enzyme activities, and the development of new therapeutic strategies.
CAT: BRP-01882
CAS: 936827-93-9
MF: C10H15N5O13P2S.xC4H12N2
MF: 507.27 (free base)
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Storage: Store at -20 °C, Always avoid freeze-thaw cycles
IUPAC Name: [(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-3-phosphonooxyoxolan-2-yl]methyl sulfo hydrogen phosphate;1,4-butanediamine
Synonyms: 3'-Adenylic acid, 5'-(dihydrogen phosphate), 5'-anhydride with sulfuric acid, compd. with 1,4-butanediamine (1:x); Phosphoadenosine phosphosulfate, butandiamine; 3'-Phosphoadenylyl sulfate, butandiamine; PAPS, butandiamine; 3'-Phosphoadenosine 5'-phosphosulfate, butandiamine; 5'-Adenylyl sulfate 3'-phosphate, butandiamine; Adenosine 3'-phosphate 5'-sulfatophosphate, butandiamine; Adenosine 5'-phosphosulfate 3'-phosphate, butandiamine
Related CAS: 482-67-7 (free base)

Adenosine 3'-phosphate 5'-phosphosulfate, histidine

Description: Adenosine 3'-phosphate 5'-phosphosulfate, L-histidine is a modified nucleotide where adenosine is phosphorylated at both the 3' and 5' positions, with a sulfate group attached to the 5' phosphate. Adenosine 3'-phosphate 5'-phosphosulfate, L-histidine is a specialized biochemical compound that combines the sulfate-donating capabilities of PAPS with the unique properties of L-histidine. This combination makes it a valuable tool for studying sulfation processes, protein interactions, enzyme activities, and potential therapeutic applications.
CAT: BRP-01883
CAS: 936827-94-0
MF: C10H15N5O13P2S.xC6H9N3O2
MF: 507.27 (free base)
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Storage: Store at -20 °C, Always avoid freeze-thaw cycles
IUPAC Name: [(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-3-phosphonooxyoxolan-2-yl]methyl sulfo hydrogen phosphate;(2S)-2-amino-3-(1H-imidazol-5-yl)propanoic acid
Synonyms: L-Histidine, compd. with 3'-adenylic acid 5'-(dihydrogen phosphate) 5'-anhydride with sulfuric acid (1:x); Phosphoadenosine phosphosulfate, L-histidine; 3'-Phosphoadenylyl sulfate, L-histidine; PAPS, L-histidine; 3'-Phosphoadenosine 5'-phosphosulfate, L-histidine; 5'-Adenylyl sulfate 3'-phosphate, L-histidine; Adenosine 3'-phosphate 5'-sulfatophosphate, L-histidine; Adenosine 5'-phosphosulfate 3'-phosphate, L-histidine
Related CAS: 482-67-7 (free base)

3'-Phosphoadenosine 5'-phosphosulfate triethylammnonium salt

Description: 3'-Phosphoadenosine 5'-phosphosulfate triethylammonium salt (PAPS-TEA) is a biochemical compound where 3'-phosphoadenosine 5'-phosphosulfate (PAPS) is stabilized as a salt with triethylammonium. 3'-Phosphoadenosine 5'-phosphosulfate triethylammonium salt (PAPS-TEA) is a key reagent in biochemical and pharmacological research, providing a stable and soluble form of PAPS for studying sulfation processes and their implications in cellular functions and drug development.
CAT: BRP-01884
CAS: 936827-87-1
MF: C10H15N5O13P2S.xC6H15N
MF: 507.27 (free base)
Purity: ≥90%
Appearance: Off-white crystalline powder
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Storage: Store at -20 °C, Always avoid freeze-thaw cycles
InChIKey: DSVQYYJXFALRJJ-KWIZKVQNSA-N
Solubility: Soluble in Water
CanonicalSMILES: CC[NH+](CC)CC.CC[NH+](CC)CC.CC[NH+](CC)CC.CC[NH+](CC)CC.C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)COP(=O)([O-])OS(=O)(=O)[O-])OP(=O)([O-])[O-])O)N
IUPAC Name: [(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-3-phosphonooxyoxolan-2-yl]methyl sulfo hydrogen phosphate;N,N-diethylethanamine
InChI: InChI=1S/C10H15N5O13P2S.4C6H15N/c11-8-5-9(13-2-12-8)15(3-14-5)10-6(16)7(27-29(17,18)19)4(26-10)1-25-30(20,21)28-31(22,23)24;4*1-4-7(5-2)6-3/h2-4,6-7,10,16H,1H2,(H,20,21)(H2,11,12,13)(H2,17,18,19)(H,22,23,24);4*4-6H2,1-3H3/t4-,6-,7-,10-;;;;/m1..../s1
Synonyms: 3'-Adenylic acid, 5'-(dihydrogen phosphate), 5'-anhydride with sulfuric acid, compd. with N,N-diethylethanamine (1:x); Phosphoadenosine phosphosulfate, TEA salt; 3'-Phosphoadenylyl sulfate, TEA salt; PAPS, TEA salt; 3'-Phosphoadenosine 5'-phosphosulfate, TEA salt; 5'-Adenylyl sulfate 3'-phosphate, TEA salt; Adenosine 3'-phosphate 5'-sulfatophosphate, TEA salt; Adenosine 5'-phosphosulfate 3'-phosphate, TEA salt
Related CAS: 482-67-7 (free base)

N-Phosphoadenosine-5'-phosphosulfate lithium salt hydrate

Description: N-Phosphoadenosine-5'-phosphosulfate lithium salt hydrate is an indispensable compound prevalent in the biomedical field, exhibiting its significant relevance in the research and development of sulfated glycosaminoglycans, integral constituents of connective tissues. Additionally, it serves as an appreciable substrate for enzymes participating in compound metabolism and detoxification mechanisms.
CAT: BRP-01885
MF: C10H15N5O13P2S·xLi·yH2O
MF: 507.27 (anhydrous free acid)
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Storage: Store at -20 °C, Always avoid freeze-thaw cycles
IUPAC Name: lithium;[[9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-[[hydroxy(sulfooxy)phosphoryl]oxymethyl]oxolan-2-yl]purin-6-yl]amino]phosphonic acid;hydrate
Synonyms: Adenosine N-phosphate 5'-phosphosulfate lithium salt hydrate; Sulfuric acid, 5'-anhydride with N-phosphono-5'-adenylic acid, lithium salt, hydrate (1:x:x)
Related CAS: 109434-21-1 (anhydrous) ; 765231-59-2 (anhydrous free acid)

2-Thio-UTP tetrasodium salt

Description: 2-ThioUTP tetrasodium salt is a potent and selective P2Y2 agonist (EC50 = 0.035, 0.35 and 1.5 μM for hP2Y2, hP2Y4 and hP2Y6 receptors, respectively).
CAT: BRP-01890
CAS: 1343364-70-4
MF: C9H11N2Na4O14P3S
MF: 588.13
Purity: ≥98% by HPLC
Appearance: Colorless transparent liquid
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Storage: Store at -20°C
InChIKey: QCBCNKBBEOQRRB-ODQFIEKDSA-J
Solubility: Soluble in Water
CanonicalSMILES: C1=CN(C(=S)NC1=O)C2C(C(C(O2)COP(=O)([O-])OP(=O)([O-])OP(=O)([O-])[O-])O)O.[Na+].[Na+].[Na+].[Na+]
IUPAC Name: tetrasodium;[[[(2R,3S,4R,5R)-3,4-dihydroxy-5-(4-oxo-2-sulfanylidenepyrimidin-1-yl)oxolan-2-yl]methoxy-oxidophosphoryl]oxy-oxidophosphoryl] phosphate
InChI: InChI=1S/C9H15N2O14P3S.4Na/c12-5-1-2-11(9(29)10-5)8-7(14)6(13)4(23-8)3-22-27(18,19)25-28(20,21)24-26(15,16)17;;;;/h1-2,4,6-8,13-14H,3H2,(H,18,19)(H,20,21)(H,10,12,29)(H2,15,16,17);;;;/q;4*+1/p-4/t4-,6-,7-,8-;;;;/m1..../s1
Synonyms: 2-Thiouridine 5'-triphosphate tetrasodium salt; 2-Thiouridine 5'-(tetrahydrogen triphosphate) tetrasodium salt; ((2R,3S,4R,5R)-3,4-dihydroxy-5-(4-oxo-2-thioxo-3,4-dihydropyrimidin-1(2H)-yl)tetrahydrofuran-2-yl)methyl triphosphate tetrasodium salt; Uridine 5'-(tetrahydrogen triphosphate), 2-thio-, sodium salt (1:4)
Related CAS: 35763-29-2 (free acid)
* Only for research. Not suitable for any diagnostic or therapeutic use.
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