Nucleosides - RNA / BOC Sciences

(E)-N'-(1-Benzyl-9-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-6-oxo-6,9-dihydro-1H-purin-2-yl)-N,N-dimethylformimidamide

Description: (E)-N'-(1-Benzyl-9-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-6-oxo-6,9-dihydro-1H-purin-2-yl)-N,N-dimethylformimidamide is a chemical compound used in organic synthesis and medicinal chemistry. It is often utilized as a precursor or intermediate in the synthesis of nucleoside analogs or other bioactive compounds.

CAT: BRP-00795

MF: C20H24N6O5

MF: 428.44

Purity: 98%

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InChIKey: ALGXQQKQSPSJBB-DJWODFLFSA-N

InChI: InChI=1S/C20H24N6O5/c1-24(2)10-22-20-23-17-14(18(30)25(20)8-12-6-4-3-5-7-12)21-11-26(17)19-16(29)15(28)13(9-27)31-19/h3-7,10-11,13,15-16,19,27-29H,8-9H2,1-2H3/b22-10+/t13-,15-,16-,19-/m1/s1

5,8-Dihydro-N,N,5-trimethyl-8-β-D-ribofuranosylpyrrolo[2',3':4,5]pyrrolo[2,3-d]pyrimidin-4-amine

Description: 5,8-Dihydro-N,N,5-trimethyl-8-β-D-ribofuranosylpyrrolo[2',3':4,5]pyrrolo[2,3-d]pyrimidin-4-amine is a chemical compound with potential biological activity. It is often studied for its potential pharmacological properties or as a building block in medicinal chemistry for the synthesis of nucleoside analogs.

CAT: BRP-00796

CAS: 2180983-51-9

MF: C16H21N5O4

MF: 347.37

Purity: 98%

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Density: 1.62±0.1 g/cm3

Boiling Point: 588.6±50.0 °C at 760 mmHg

InChIKey: GIPKNLNHAZHJMS-RVXWVPLUSA-N

CanonicalSMILES: CN1C=CC2=C1C3=C(N2C4C(C(C(O4)CO)O)O)N=CN=C3N(C)C

IUPAC Name: (2R,3R,4S,5R)-2-[12-(dimethylamino)-3-methyl-3,7,9,11-tetrazatricyclo[6.4.0.02,6]dodeca-1(8),2(6),4,9,11-pentaen-7-yl]-5-(hydroxymethyl)oxolane-3,4-diol

InChI: InChI=1S/C16H21N5O4/c1-19(2)14-10-11-8(4-5-20(11)3)21(15(10)18-7-17-14)16-13(24)12(23)9(6-22)25-16/h4-5,7,9,12-13,16,22-24H,6H2,1-3H3/t9-,12-,13-,16-/m1/s1

Synonyms: Pyrrolo[2',3':4,5]pyrrolo[2,3-d]pyrimidin-4-amine, 5,8-dihydro-N,N,5-trimethyl-8-β-D-ribofuranosyl-; (2R,3R,4S,5R)-2-(4-(Dimethylamino)-5-methylpyrrolo[2',3':4,5]pyrrolo[2,3-d]pyrimidin-8(5H)-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol

5-O-DMT-N2-Dimethylformamide-2-O-methylguanosine

Description: 5-O-DMT-N2-Dimethylformamide-2-O-methylguanosine is a modified nucleoside compound commonly used in RNA synthesis and modification studies. It is often employed as a building block for the synthesis of RNA molecules with specific modifications for various biological and research purposes.

CAT: BRP-00797

CAS: 1858223-91-2

MF: C35H38N6O7

MF: 654.71

Purity: 97%

Appearance: White powder

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Storage: Store at 2-8 °C, Keep in a dark and dry place

Density: 1.33±0.1 g/cm3

Boiling Point: 848.7±75.0 °C at 760 mmHg

InChIKey: SBJHBQZDABMKCF-JHZZHVAFSA-N

CanonicalSMILES: CN(C)C=NC1=NC2=C(C(=O)N1)N=CN2C3C(C(C(O3)COC(C4=CC=CC=C4)(C5=CC=C(C=C5)OC)C6=CC=C(C=C6)OC)O)OC

IUPAC Name: N'-[9-[(2R,3R,4R,5R)-5-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-4-hydroxy-3-methoxyoxolan-2-yl]-6-oxo-1H-purin-2-yl]-N,N-dimethylmethanimidamide

InChI: InChI=1S/C35H38N6O7/c1-40(2)20-37-34-38-31-28(32(43)39-34)36-21-41(31)33-30(46-5)29(42)27(48-33)19-47-35(22-9-7-6-8-10-22,23-11-15-25(44-3)16-12-23)24-13-17-26(45-4)18-14-24/h6-18,20-21,27,29-30,33,42H,19H2,1-5H3,(H,38,39,43)/t27-,29-,30-,33-/m1/s1

Synonyms: N'-(9-((2R,3R,4R,5R)-5-((Bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-hydroxy-3-methoxytetrahydrofuran-2-yl)-6-oxo-6,9-dihydro-1H-purin-2-yl)-N,N-dimethylformimidamide; 5'-O-DMT-N2-DMF-2'-O-methylguanosine; N2-dmf-DMT-2'-OMe-Gr; N2-dimethylformamidine-5'-O-(4,4'-dimethoxytrityl)-2'-O-methyl-Guanosine

(E)-N2-Dimethylformamide-2-O-methylguanosine

Description: (E)-N2-Dimethylformamide-2-O-methylguanosine is a modified nucleoside compound used in RNA synthesis and modification studies. It is commonly employed as a building block for the synthesis of RNA molecules with specific modifications, allowing researchers to investigate RNA structure, function, and interactions.

CAT: BRP-00798

CAS: 1951424-87-5

MF: C14H20N6O5

MF: 352.35

Purity: 98%

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Density: 1.63±0.1 g/cm3

Boiling Point: 672.2±65.0 °C at 760 mmHg

InChIKey: KDQQTCFKBCWYFL-GTACIXLRSA-N

CanonicalSMILES: CN(C)C=NC1=NC2=C(C(=O)N1)N=CN2C3C(C(C(O3)CO)O)OC

IUPAC Name: (E)-N'-[9-[(2R,3R,4R,5R)-4-hydroxy-5-(hydroxymethyl)-3-methoxyoxolan-2-yl]-6-oxo-1H-purin-2-yl]-N,N-dimethylmethanimidamide

InChI: InChI=1S/C14H20N6O5/c1-19(2)5-16-14-17-11-8(12(23)18-14)15-6-20(11)13-10(24-3)9(22)7(4-21)25-13/h5-7,9-10,13,21-22H,4H2,1-3H3,(H,17,18,23)/b16-5+/t7-,9-,10-,13-/m1/s1

Synonyms: (E)-N-[(Dimethylamino)methylene]-2'-O-methylguanosine; (E)-N'-(9-((2R,3R,4R,5R)-4-Hydroxy-5-(hydroxymethyl)-3-methoxytetrahydrofuran-2-yl)-6-oxo-6,9-dihydro-1H-purin-2-yl)-N,N-dimethylformimidamide

Related CAS: 183737-04-4 (N-[(Dimethylamino)methylene]-2'-O-methylguanosine)

[N(E)]-N-[(Dimethylamino)methylene]guanosine

Description: [N(E)]-N-[(Dimethylamino)methylene]guanosine is a modified nucleoside compound commonly utilized in biochemical research, particularly in RNA studies. This modification is often used to investigate RNA structure, function, and interactions, providing valuable insights into biological processes such as RNA folding, RNA-protein interactions, and RNA catalysis.

CAT: BRP-00799

CAS: 1055407-32-3

MF: C13H18N6O5

MF: 338.32

Purity: 98%

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Density: 1.77±0.1 g/cm3

Boiling Point: 708.5±70.0 °C at 760 mmHg

InChIKey: WDAVDBAMSKZBEN-PZYHSTABSA-N

CanonicalSMILES: CN(C)C=NC1=NC2=C(C(=O)N1)N=CN2C3C(C(C(O3)CO)O)O

IUPAC Name: (E)-N'-[9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-6-oxo-1H-purin-2-yl]-N,N-dimethylmethanimidamide

InChI: InChI=1S/C13H18N6O5/c1-18(2)4-15-13-16-10-7(11(23)17-13)14-5-19(10)12-9(22)8(21)6(3-20)24-12/h4-6,8-9,12,20-22H,3H2,1-2H3,(H,16,17,23)/b15-4+/t6-,8-,9-,12-/m1/s1

Synonyms: (E)-N'-(9-((2R,3R,4S,5R)-3,4-Dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-6-oxo-6,9-dihydro-3H-purin-2-yl)-N,N-dimethylformimidamide; Guanosine, N-[(dimethylamino)methylene]-, [N(E)]-; (E)-N2-DMF-rG; N-dimethylaminomethylene guanosine

Related CAS: 17331-16-7 (N-[(Dimethylamino)methylene]guanosine)

2'-O-TBDMS-N2-DMF-rG

Description: 2'-O-TBDMS-N2-DMF-rG is a modified nucleoside commonly employed in RNA synthesis and modification studies. It contains a guanosine base with modifications at the 2'-position (TBDMS) and N2 position (DMF). The TBDMS group protects the 2'-hydroxyl group, while the DMF group is attached to the N2 position. This modification allows researchers to introduce specific functionalities into RNA molecules for various research purposes, such as structural studies, RNA-protein interactions, or RNA labeling experiments, providing valuable insights into RNA biology and function.

CAT: BRP-00800

CAS: 126922-63-2

MF: C19H32N6O5Si

MF: 452.58

Purity: 98%

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Density: 1.34±0.1 g/cm3

InChIKey: ILIKLOCTYDXXNJ-LSCFUAHRSA-N

CanonicalSMILES: CC(C)(C)[Si](C)(C)OC1C(C(OC1N2C=NC3=C2N=C(NC3=O)N=CN(C)C)CO)O

IUPAC Name: N'-[9-[(2R,3R,4R,5R)-3-[tert-butyl(dimethyl)silyl]oxy-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-6-oxo-1H-purin-2-yl]-N,N-dimethylmethanimidamide

InChI: InChI=1S/C19H32N6O5Si/c1-19(2,3)31(6,7)30-14-13(27)11(8-26)29-17(14)25-10-20-12-15(25)22-18(23-16(12)28)21-9-24(4)5/h9-11,13-14,17,26-27H,8H2,1-7H3,(H,22,23,28)/t11-,13-,14-,17-/m1/s1

Synonyms: Guanosine, N-[(dimethylamino)methylene]-2'-O-[(1,1-dimethylethyl)dimethylsilyl]-; N-[(Dimethylamino)methylene]-2'-O-[(1,1-dimethylethyl)dimethylsilyl]guanosine; N'-(9-((2R,3R,4R,5R)-3-((tert-Butyldimethylsilyl)oxy)-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-6-oxo-6,9-dihydro-1H-purin-2-yl)-N,N-dimethylformimidamide

5-Bromotubercidin

Description: 5-Bromotubercidin is a chemical compound commonly utilized in biochemical research and drug development. It belongs to the class of tubercidin analogs and is known for its inhibitory effects on various enzymes, including kinases.

CAT: BRP-00801

CAS: 21193-80-6

MF: C11H13BrN4O4

MF: 345.15

Purity: 97%

Appearance: White to off-white solid

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Storage: Store at 2-8 °C, protect from light

Density: 2.26±0.1 g/cm3

Melting Point: 232 °C

Boiling Point: 686.9±55.0 °C at 760 mmHg

InChIKey: ZWTPRQXZXQEKFT-IOSLPCCCSA-N

Solubility: Soluble in DMSO (Slightly), Methanol (Slightly)

CanonicalSMILES: C1=C(C2=C(N=CN=C2N1C3C(C(C(O3)CO)O)O)N)Br

IUPAC Name: (2R,3R,4S,5R)-2-(4-amino-5-bromopyrrolo[2,3-d]pyrimidin-7-yl)-5-(hydroxymethyl)oxolane-3,4-diol

InChI: InChI=1S/C11H13BrN4O4/c12-4-1-16(10-6(4)9(13)14-3-15-10)11-8(19)7(18)5(2-17)20-11/h1,3,5,7-8,11,17-19H,2H2,(H2,13,14,15)/t5-,7-,8-,11-/m1/s1

Synonyms: (2R,3R,4S,5R)-2-(4-Amino-5-bromo-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol; Bromotubercidin; 5-Bromo-7-β-D-ribofuranosyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine; NSC103802

O2',O3',O5'-Tribenzoyl-5-methyl-2-thiouridine

Description: O2',O3',O5'-Tribenzoyl-5-methyl-2-thiouridine is a modified nucleoside compound often used in RNA research and modification studies. It contains a uridine base with modifications at the 2nd position (thio), and the 2', 3', and 5' hydroxyl groups are tribenzoylated. This modification is utilized to study RNA structure, function, and interactions, providing insights into RNA biology and potential therapeutic applications.

CAT: BRP-00802

CAS: 75921-08-3

MF: C31H26N2O8S

MF: 586.61

Purity: 98%

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Density: 1.43±0.1 g/cm3

InChIKey: JEAZFXFXZLAZLW-DLGLWYJGSA-N

CanonicalSMILES: CC1=CN(C(=S)NC1=O)C2C(C(C(O2)COC(=O)C3=CC=CC=C3)OC(=O)C4=CC=CC=C4)OC(=O)C5=CC=CC=C5

IUPAC Name: [(2R,3R,4R,5R)-3,4-dibenzoyloxy-5-(5-methyl-4-oxo-2-sulfanylidenepyrimidin-1-yl)oxolan-2-yl]methyl benzoate

InChI: InChI=1S/C31H26N2O8S/c1-19-17-33(31(42)32-26(19)34)27-25(41-30(37)22-15-9-4-10-16-22)24(40-29(36)21-13-7-3-8-14-21)23(39-27)18-38-28(35)20-11-5-2-6-12-20/h2-17,23-25,27H,18H2,1H3,(H,32,34,42)/t23-,24-,25-,27-/m1/s1

Synonyms: (2R,3R,4R,5R)-2-((Benzoyloxy)methyl)-5-(5-methyl-4-oxo-2-thioxo-3,4-dihydropyrimidin-1(2H)-yl)tetrahydrofuran-3,4-diyl dibenzoate; Uridine, 5-methyl-2-thio-, 2',3',5'-tribenzoate

2',3'-O-Isopropylidenecytidine sulfate

Description: 2',3'-O-Isopropylidenecytidine sulfate is a modified nucleoside compound frequently employed in RNA synthesis and modification studies. It contains a cytidine base with protection at the 2' and 3' hydroxyl groups by isopropylidene and is in the form of a sulfate salt.

CAT: BRP-00803

CAS: 1955522-00-5

MF: C12H19N3O9S

MF: 381.36

Purity: 98%

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InChIKey: WEIXBFRDOMNWIS-RQDZQORCSA-N

CanonicalSMILES: CC1(OC2C(OC(C2O1)N3C=CC(=NC3=O)N)CO)C.OS(=O)(=O)O

IUPAC Name: 1-[(3aR,4R,6R,6aR)-6-(hydroxymethyl)-2,2-dimethyl-3a,4,6,6a-tetrahydrofuro[3,4-d][1,3]dioxol-4-yl]-4-aminopyrimidin-2-one;sulfuric acid

InChI: InChI=1S/C12H17N3O5.H2O4S/c1-12(2)19-8-6(5-16)18-10(9(8)20-12)15-4-3-7(13)14-11(15)17;1-5(2,3)4/h3-4,6,8-10,16H,5H2,1-2H3,(H2,13,14,17);(H2,1,2,3,4)/t6-,8-,9-,10-;/m1./s1

Synonyms: 4-Amino-1-((3aR,4R,6R,6aR)-6-(hydroxymethyl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)pyrimidin-2(1H)-one sulfate; 2',3'-Isopropylidenecytidine sulfate; 2',3'-O-(1-Methylethylidene)cytidine sulfate

Related CAS: 362-42-5 (free base)

1-(β-D-lyxofuranosyl)uracil

Description: 1-(β-D-lyxofuranosyl)uracil is a nucleoside compound commonly used in nucleic acid research and drug development. This modified nucleoside is employed in the study of nucleic acid structure and function, and can be used as an analog in the synthesis of oligonucleotides. Additionally, it has potential applications in the development of antiviral and anticancer therapeutics by mimicking natural nucleosides and interfering with nucleic acid metabolism.

CAT: BRP-00804

CAS: 4348-61-2

MF: C9H12N2O6

MF: 244.20

Purity: 98%

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Density: 1.674±0.06 g/cm3 (Predicted)

Melting Point: 203-204 °C

InChIKey: DRTQHJPVMGBUCF-YDKYIBAVSA-N

CanonicalSMILES: C1=CN(C(=O)NC1=O)C2C(C(C(O2)CO)O)O

IUPAC Name: 1-[(2R,3S,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidine-2,4-dione

InChI: InChI=1S/C9H12N2O6/c12-3-4-6(14)7(15)8(17-4)11-2-1-5(13)10-9(11)16/h1-2,4,6-8,12,14-15H,3H2,(H,10,13,16)/t4-,6+,7+,8-/m1/s1

Synonyms: 1-((2R,3S,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyrimidine-2,4(1H,3H)-dione; 1-β-D-lyxofuranosyl-uracil; 2,4(1H,3H)-Pyrimidinedione, 1-β-D-lyxofuranosyl-

(E)-Ethyl 3-(1-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)acrylate

Description: (E)-Ethyl 3-(1-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)acrylate is a modified nucleoside derivative used in biochemical and pharmaceutical research. The modifications enhance its utility in studying nucleic acid interactions and functions, and it can serve as an intermediate in the synthesis of nucleoside analogs. These analogs have potential therapeutic applications, particularly in antiviral and anticancer treatments, by interfering with nucleic acid metabolism and replication processes.

CAT: BRP-00805

CAS: 123881-85-6

MF: C14H18N2O8

MF: 342.30

Purity: 98%

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Storage: Store at 2-8 °C

Density: 1.583±0.06 g/cm3

InChIKey: ATSFSUUXRHMGQU-BGFIHSBQSA-N

CanonicalSMILES: CCOC(=O)C=CC1=CN(C(=O)NC1=O)C2C(C(C(O2)CO)O)O

IUPAC Name: ethyl (E)-3-[1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-2,4-dioxopyrimidin-5-yl]prop-2-enoate

InChI: InChI=1S/C14H18N2O8/c1-2-23-9(18)4-3-7-5-16(14(22)15-12(7)21)13-11(20)10(19)8(6-17)24-13/h3-5,8,10-11,13,17,19-20H,2,6H2,1H3,(H,15,21,22)/b4-3+/t8-,10-,11-,13-/m1/s1

Synonyms: 2-Propenoic acid, 3-[1,2,3,4-tetrahydro-2,4-dioxo-1-β-D-ribofuranosyl-5-pyrimidinyl]-, ethyl ester, (E)-

6-Fluoro-3,4-dihydro-3-oxo-4-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)pyrazinecarboxamide

Description: 6-Fluoro-3,4-dihydro-3-oxo-4-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)pyrazinecarboxamide is a modified nucleoside analog used in biochemical research and pharmaceutical development. The modifications enhance its stability and facilitate its incorporation into nucleic acids. It is often utilized in the synthesis of nucleoside analogs for studying nucleic acid interactions, function, and potential therapeutic applications, particularly in the development of antiviral and anticancer agents.

CAT: BRP-00807

CAS: 499785-96-5

MF: C16H18FN3O9

MF: 415.33

Purity: 98%

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Density: 1.61±0.1 g/cm3

Boiling Point: 524.4±60.0 °C at 760 mmHg

InChIKey: IVDSFFUXGZDUGN-RVXWVPLUSA-N

CanonicalSMILES: CC(=O)OCC1C(C(C(O1)N2C=C(N=C(C2=O)C(=O)N)F)OC(=O)C)OC(=O)C

IUPAC Name: [(2R,3R,4R,5R)-3,4-diacetyloxy-5-(3-carbamoyl-5-fluoro-2-oxopyrazin-1-yl)oxolan-2-yl]methyl acetate

InChI: InChI=1S/C16H18FN3O9/c1-6(21)26-5-9-12(27-7(2)22)13(28-8(3)23)16(29-9)20-4-10(17)19-11(14(18)24)15(20)25/h4,9,12-13,16H,5H2,1-3H3,(H2,18,24)/t9-,12-,13-,16-/m1/s1

Synonyms: Pyrazinecarboxamide, 6-fluoro-3,4-dihydro-3-oxo-4-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)-; Acetic acid (2R,3R,4R,5R)-3,4-diacetoxy-5-(3-carbamoyl-5-fluoro-2-oxo-2H-pyrazin-1-yl)-tetrahydro-furan-2-ylmethyl ester; (2R,3R,4R,5R)-2-(Acetoxymethyl)-5-(3-carbamoyl-5-fluoro-2-oxopyrazin-1(2H)-yl)tetrahydrofuran-3,4-diyl diacetate

2-O-Ethyl-2'-O-methyluridine

Description: 2-O-Ethyl-2'-O-methyluridine is a modified nucleoside used in biochemical research, particularly in the study of RNA synthesis and modification. These modifications increase the stability and resistance to enzymatic degradation of the nucleoside, making it useful in the development of therapeutic oligonucleotides and the study of RNA structure and function.

CAT: BRP-00808

CAS: 1352173-49-9

MF: C12H18N2O6

MF: 286.28

Purity: 98%

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Density: 1.47±0.1 g/cm3

Boiling Point: 466.2±55.0 °C at 760 mmHg

InChIKey: NZNRDRCBHUXJKX-QCNRFFRDSA-N

CanonicalSMILES: CCOC1=NC(=O)C=CN1C2C(C(C(O2)CO)O)OC

IUPAC Name: 2-ethoxy-1-[(2R,3R,4R,5R)-4-hydroxy-5-(hydroxymethyl)-3-methoxyoxolan-2-yl]pyrimidin-4-one

InChI: InChI=1S/C12H18N2O6/c1-3-19-12-13-8(16)4-5-14(12)11-10(18-2)9(17)7(6-15)20-11/h4-5,7,9-11,15,17H,3,6H2,1-2H3/t7-,9-,10-,11-/m1/s1

Synonyms: 2'-O-Methyl-2-O-ethyluridine; 2-Ethoxy-1-((2R,3R,4R,5R)-4-hydroxy-5-(hydroxymethyl)-3-methoxytetrahydrofuran-2-yl)pyrimidin-4(1H)-one

S-(5')-Adenosyl-3-thiopropylamine

Description: S-(5')-Adenosyl-3-thiopropylamine is a modified nucleoside compound used in biochemical research, particularly in the study of enzyme mechanisms and metabolic pathways. This compound consists of an adenosine moiety linked to a 3-thiopropylamine group via a sulfur atom at the 5' position. It serves as a cofactor or substrate analog in various enzymatic reactions, providing insights into the role of sulfur-containing nucleosides in biological processes and potential therapeutic applications.

CAT: BRP-00810

CAS: 53186-57-5

MF: C13H20N6O3S

MF: 340.40

Purity: 98%

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Density: 1.78±0.1 g/cm3

Boiling Point: 683.7±65.0 °C at 760 mmHg

InChIKey: FUSRAALGPJJIRO-QYVSTXNMSA-N

CanonicalSMILES: C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CSCCCN)O)O)N

IUPAC Name: (2S,3S,4R,5R)-2-(3-aminopropylsulfanylmethyl)-5-(6-aminopurin-9-yl)oxolane-3,4-diol

InChI: InChI=1S/C13H20N6O3S/c14-2-1-3-23-4-7-9(20)10(21)13(22-7)19-6-18-8-11(15)16-5-17-12(8)19/h5-7,9-10,13,20-21H,1-4,14H2,(H2,15,16,17)/t7-,9-,10-,13-/m1/s1

Synonyms: S-Adenosyl-3-thiopropylamine; 5'-S-(3-Aminopropyl)-5'-thioadenosine; 5''-(Aminopropylthio)-5''-deoxy-adenosine; (2R,3R,4S,5S)-2-(6-amino-9H-purin-9-yl)-5-((3-aminopropylthio)methyl)tetrahydrofuran-3,4-diol

Related CAS: 99019-00-8 (sulfate)

N4-Ac-2'-O-4'-C-Locked-Cr

Description: N4-Ac-2'-O-4'-C-Locked-Cr is a modified nucleoside used in oligonucleotide synthesis. It consists of an acetyl group (Ac) at the N4 position of the cytosine, a 2'-O modification, and a 4'-carbon locked cytosine (Locked-Cr). This modification is designed to stabilize the oligonucleotide structure and alter its properties for specific applications in nucleic acid research and biotechnology.

CAT: BRP-00986

CAS: 391199-75-0

MF: C12H15N3O6

MF: 297.27

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Inquiry

Density: 1.77±0.1 g/cm3

Melting Point: 223-225 °C (dec.)

InChIKey: DLDUBZSJKKUTMP-KLBPJQLPSA-N

CanonicalSMILES: CC(=O)NC1=NC(=O)N(C=C1)C2C3C(C(O2)(CO3)CO)O

IUPAC Name: N-[1-[(1S,3R,4R,7S)-7-hydroxy-1-(hydroxymethyl)-2,5-dioxabicyclo[2.2.1]heptan-3-yl]-2-oxopyrimidin-4-yl]acetamide

InChI: InChI=1S/C12H15N3O6/c1-6(17)13-7-2-3-15(11(19)14-7)10-8-9(18)12(4-16,21-10)5-20-8/h2-3,8-10,16,18H,4-5H2,1H3,(H,13,14,17,19)/t8-,9+,10-,12+/m1/s1

Synonyms: N4-acetyl-2'-O-4'-C-Locked-cytidine; Acetamide, N-[1-[2,5-anhydro-4-C-(hydroxymethyl)-α-L-lyxofuranosyl]-1,2-dihydro-2-oxo-4-pyrimidinyl]-; LNA C(Ac)

N4-Dibutylformamidine-2'-O-Me-Cr

Description: N4-Dibutylformamidine-2'-O-Me-Cr is a modified nucleoside used in oligonucleotide synthesis. It consists of a dibutylformamidine group attached to the N4 position of cytosine, a methyl (Me) group at the 2' position of ribose, and a modified cytosine (Cr). This modification alters the properties of the oligonucleotide and can be utilized for specific applications in nucleic acid research and biotechnology.

CAT: BRP-00987

MF: C19H32N4O5

MF: 396.49

Purity: ≥98% by HPLC

Appearance: White powder

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Storage: Store at 2-8 °C, Keep in a dark and dry place

InChIKey: MMQXUCDIZCUQOH-VDHUWJSZSA-N

IUPAC Name: N,N-dibutyl-N'-(1-((2R,3R,4R,5R)-4-hydroxy-5-(hydroxymethyl)-3-methoxytetrahydrofuran-2-yl)-2-oxo-1,2-dihydropyrimidin-4-yl)formimidamide

InChI: InChI=1S/C19H32N4O5/c1-4-6-9-22(10-7-5-2)13-20-15-8-11-23(19(26)21-15)18-17(27-3)16(25)14(12-24)28-18/h8,11,13-14,16-18,24-25H,4-7,9-10,12H2,1-3H3/t14-,16-,17-,18-/m1/s1

Synonyms: N4-dibutylformamidine-2'-O-methyl-cytidine

N1-Methylene pivalate-N2-dibutylformamidine-2'-O-Me-Gr

Description: N1-Methylene pivalate-N2-dibutylformamidine-2'-O-Me-Gr is a modified nucleoside used in oligonucleotide synthesis. It consists of a methylene pivalate group attached to the N1 position of guanine, a dibutylformamidine group attached to the N2 position of guanine, a methyl (Me) group at the 2' position of ribose, and a modified guanine (Gr). This modification alters the properties of the oligonucleotide and can be employed for specific applications in nucleic acid research and biotechnology.

CAT: BRP-00988

MF: C26H42N6O7

MF: 550.66

Purity: ≥98% by HPLC

Appearance: White powder

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Storage: Store at 2-8 °C, Keep in a dark and dry place

InChIKey: FJYUEQOQXMHZLF-ZDXOVATRSA-N

IUPAC Name: (2-(((dibutylamino)methylene)amino)-9-((2R,3R,4R,5R)-4-hydroxy-5-(hydroxymethyl)-3-methoxytetrahydrofuran-2-yl)-6-oxo-6,9-dihydro-1H-purin-1-yl)methyl pivalate

InChI: InChI=1S/C26H42N6O7/c1-7-9-11-30(12-10-8-2)14-28-25-29-21-18(22(35)32(25)16-38-24(36)26(3,4)5)27-15-31(21)23-20(37-6)19(34)17(13-33)39-23/h14-15,17,19-20,23,33-34H,7-13,16H2,1-6H3/t17-,19-,20-,23-/m1/s1

Synonyms: N1-methylene pivalate-N2-dibutylformamidine-2'-O-methyl-guanosine

N2-Dibutylformamidine-2'-O-Me-Gr

Description: N2-Dibutylformamidine-2'-O-Me-Gr is a modified nucleoside used in oligonucleotide synthesis. It consists of a dibutylformamidine group attached to the N2 position of guanine, a methyl (Me) group at the 2' position of ribose, and a modified guanine (Gr). This modification can alter the properties of the oligonucleotide for specific applications in nucleic acid research and biotechnology.

CAT: BRP-00989

MF: C20H32N6O5

MF: 436.51

Purity: ≥98% by HPLC

Appearance: White powder

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Storage: Store at 2-8 °C, Keep in a dark and dry place

InChIKey: KZJIRTOCSLCQKS-NVQRDWNXSA-N

IUPAC Name: N,N-dibutyl-N'-(9-((2R,3R,4R,5R)-4-hydroxy-5-(hydroxymethyl)-3-methoxytetrahydrofuran-2-yl)-6-oxo-6,9-dihydro-1H-purin-2-yl)formimidamide

InChI: InChI=1S/C20H32N6O5/c1-4-6-8-25(9-7-5-2)11-22-20-23-17-14(18(29)24-20)21-12-26(17)19-16(30-3)15(28)13(10-27)31-19/h11-13,15-16,19,27-28H,4-10H2,1-3H3,(H,23,24,29)/t13-,15-,16-,19-/m1/s1

Synonyms: N2-dibutylformamidine-2'-O-methyl-guanosine

8-Br-N2-iBu-2'-OMe-Gr

Description: 8-Br-N2-iBu-2'-OMe-Gr is a modified nucleoside used in oligonucleotide synthesis. It consists of a bromine (Br) atom at the 8th position of guanine, an isobutyl (iBu) group attached to the N2 position of guanine, a methyl (Me) group at the 2' position of ribose, and a modified guanine (Gr). This modification can introduce specific properties or functionalities to the oligonucleotide for various applications in nucleic acid research and biotechnology.

CAT: BRP-00990

CAS: 2920231-98-5

MF: C15H20BrN5O6

MF: 446.25

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Inquiry

Density: 1.93±0.1 g/cm3

InChIKey: VMDRFWCYFGNAGO-HTVVRFAVSA-N

CanonicalSMILES: CC(C)C(=O)NC1=NC2=C(C(=O)N1)N=C(N2C3C(C(C(O3)CO)O)OC)Br

IUPAC Name: N-[8-bromo-9-[(2R,3R,4R,5R)-4-hydroxy-5-(hydroxymethyl)-3-methoxyoxolan-2-yl]-6-oxo-1H-purin-2-yl]-2-methylpropanamide

InChI: InChI=1S/C15H20BrN5O6/c1-5(2)11(24)19-15-18-10-7(12(25)20-15)17-14(16)21(10)13-9(26-3)8(23)6(4-22)27-13/h5-6,8-9,13,22-23H,4H2,1-3H3,(H2,18,19,20,24,25)/t6-,8-,9-,13-/m1/s1

Synonyms: 8-bromo-N2-isobutyryl-2'-O-methyl-guanosine; N2-Isobutyryl-8-bromo-2'-O-methyl-guanosine; N-(8-bromo-9-((2R,3R,4R,5R)-4-hydroxy-5-(hydroxymethyl)-3-methoxytetrahydrofuran-2-yl)-6-oxo-6,9-dihydro-1H-purin-2-yl)isobutyramide; N2-iBu-8-Br-2'-O-Me-G

N4-Ac-5-I-2'-O-Me-Cr

Description: N4-Ac-5-I-2'-O-Me-Cr is a modified nucleoside used in oligonucleotide synthesis. It consists of an acetyl group (Ac) at the N4 position of cytosine, an iodine atom (I) at the 5th position of cytosine, a methyl (Me) group at the 2' position of ribose, and a modified cytosine (Cr). This modification can impart specific properties or functionalities to the oligonucleotide for various applications in nucleic acid research and biotechnology.

CAT: BRP-00991

CAS: 1402062-84-3

MF: C12H16IN3O6

MF: 425.18

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Inquiry

Density: 2.05±0.1 g/cm3

InChIKey: UKLQCCOIWJBTQA-TURQNECASA-N

CanonicalSMILES: CC(=O)NC1=NC(=O)N(C=C1I)C2C(C(C(O2)CO)O)OC

IUPAC Name: N-[1-[(2R,3R,4R,5R)-4-hydroxy-5-(hydroxymethyl)-3-methoxyoxolan-2-yl]-5-iodo-2-oxopyrimidin-4-yl]acetamide

InChI: InChI=1S/C12H16IN3O6/c1-5(18)14-10-6(13)3-16(12(20)15-10)11-9(21-2)8(19)7(4-17)22-11/h3,7-9,11,17,19H,4H2,1-2H3,(H,14,15,18,20)/t7-,8-,9-,11-/m1/s1

Synonyms: N4-Acetyl-5-iodo-2'-O-methyl-cytidine; N-Acetyl-5-iodo-2'-O-methylcytidine; N-(1-((2R,3R,4R,5R)-4-hydroxy-5-(hydroxymethyl)-3-methoxytetrahydrofuran-2-yl)-5-iodo-2-oxo-1,2-dihydropyrimidin-4-yl)acetamide