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Specialized nucleoside phosphoramidites

5′-CP™ & scpBNA™ phosphoramidites

Six research-use building blocks based on licensed 5′-CP™ and scpBNA™ technologies. Compare the chemistries, view pack prices and select products for your oligonucleotide research.

For research use only.

scpBNA™ and 5′-CP™ are Luxna Biotech trademarks. Products are supplied through WuXi’s resale arrangement with Summit Pharmaceuticals International.

scpBNA™

RNA affinity and exonuclease resistance

Reported model oligonucleotides showed LNA-comparable RNA affinity and greater resistance to 3′-exonuclease degradation than LNA and unmodified DNA. [R3–R4]

MeC(Bz) · T

scpBNA™ scaffold

5′-CP™

DNA-gap chemistry for balancing activity and tolerability

Reduced late-onset neurotoxicity with retained target knockdown through 5′-CP incorporation at DNA-gap position 3 with a 5′-adjacent phosphodiester linkage in a mouse ASO model. [R2]

A(Bz) · G(dmf) · MeC(Bz) · T

5′-CP™ scaffold

Preclinical findings; performance depends on sequence, modification position and backbone design.

Six research building blocks

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scpBNA™ · MeC and T

scpBNA™ MeC(Bz) amidite

STA-LB00001

CAS No. 1807471-41-5

Protected monomer structure of scpBNA™ MeC(Bz) amidite

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Chemical identity & selected SKU

(1R,4R,5R,7R)-5-(4-benzamido-5-methyl-2-oxopyrimidin-1(2H)-yl)-1-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-3,6-dioxaspiro[bicyclo[2.2.1]heptane-2,1'-cyclopropan]-7-yl (2-cyanoethyl) diisopropylphosphoramidite

STA-LB00001-1GM

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scpBNA™ T amidite

STA-LB00002

CAS No. 1784750-25-9

Protected monomer structure of scpBNA™ T amidite

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Chemical identity & selected SKU

(1R,4R,5R,7S)-1-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-5-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,6-dioxaspiro[bicyclo[2.2.1]heptane-2,1'-cyclopropan]-7-yl (2-cyanoethyl) diisopropylphosphoramidite

STA-LB00002-1GM

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5′-CP™ · A, G, MeC and T

5′-CP™ A(Bz) amidite

STA-LB00003

CAS No. Not assigned

Protected monomer structure of 5′-CP™ A(Bz) amidite

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(2S,3S,5R)-5-(6-benzamido-9H-purin-9-yl)-2-(1-(trityloxy)cyclopropyl)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite

STA-LB00003-1GM

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5′-CP™ G(dmf) amidite

STA-LB00004

CAS No. Not assigned

Protected monomer structure of 5′-CP™ G(dmf) amidite

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Chemical identity & selected SKU

2-cyanoethyl ((2S,3S,5R)-5-(2-(((dimethylamino)methylene)amino)-6-oxo-1,6-dihydro-9H-purin-9-yl)-2-(1-(trityloxy)cyclopropyl)tetrahydrofuran-3-yl) diisopropylphosphoramidite

STA-LB00004-1GM

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5′-CP™ MeC(Bz) amidite

STA-LB00005

CAS No. 2460633-39-8

Protected monomer structure of 5′-CP™ MeC(Bz) amidite

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Chemical identity & selected SKU

(2S,3S,5R)-5-(4-benzamido-5-methyl-2-oxopyrimidin-1(2H)-yl)-2-(1-((4-methoxyphenyl)diphenylmethoxy)cyclopropyl)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite

STA-LB00005-1GM

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5′-CP™ T amidite

STA-LB00006

CAS No. 2460633-31-0

Protected monomer structure of 5′-CP™ T amidite

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Chemical identity & selected SKU

2-cyanoethyl ((2S,3S,5R)-2-(1-((4-methoxyphenyl)diphenylmethoxy)cyclopropyl)-5-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)tetrahydrofuran-3-yl) diisopropylphosphoramidite

STA-LB00006-1GM

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5′-CP™ · Published evidence

Investigate the DNA gap and its adjacent linkage

A, G, MeC and T monomers support base-matched substitution at selected DNA-gap positions. Published work examines nucleoside placement and local PS/PO changes as connected variables in antisense activity and tolerability. [R1–R2]

In a mouse ASO model, a gap-position-3 substitution paired with a 5′-adjacent PO linkage reduced late-onset neurotoxicity while maintaining Mapt knockdown in the hippocampus and lumbar cord. [R2]

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5′-CP™ scaffold
Read the 5′-CP technical noteFour-base duplex data, nuclease resistance, RNase H and published synthesis context

5′-Cyclopropylene alters the local 5′ sugar environment of a DNA nucleoside while retaining RNA–DNA duplex formation. Model 12-mers containing a single 5′-CP substitution showed small, base-dependent decreases in melting temperature (0.9–2.4 °C). [R1]

Four-base RNA duplex data

Base at the substitution siteReference Tm5′-CP TmChange
T47.8 °C45.7 °C−2.1 °C
C / MeC53.5 °C52.6 °C−0.9 °C
A46.3 °C43.9 °C−2.4 °C
G52.4 °C50.7 °C−1.7 °C
One substitution in a 12-mer, 5′-d(GCGTTXTTTGCT)-3′, with a base-matched RNA complement. Conditions: 4 µM each strand, 10 mM phosphate, pH 7.2, 100 mM NaCl; three measurements. The MeC construct is compared with natural C, so that row also includes a base-methylation difference. [R1, Table 44]

Nuclease resistance and RNase H

5′-CP-T model constructs show increased nuclease resistance while retaining RNase H-mediated RNA cleavage. In a venom-phosphodiesterase assay, the terminal 5′-CP-T model retained approximately 70% uncleaved oligonucleotide at 40 minutes, versus approximately 30% for the terminal single-PS comparator. In a separate E. coli RNase H assay, constructs with two and three 5′-CP-T residues gave 46% and 27% RNA cleavage, respectively, versus 31% for the reference. [R1, Examples 11–12]

Published incorporation conditions

ParameterPublished conditions — patent Example 9
Amidite and activator0.1 M amidite in anhydrous acetonitrile; 0.25 M 4,5-dicyanoimidazole.
CouplingExtend coupling time to four 240-second cycles for the modified amidite and the nucleotide introduced immediately afterward.
Capping200 seconds.
DeblockingTwo 120-second cycles.
Cleavage and base deprotection28% aqueous ammonia: 1.5 h at room temperature, then at least 5 h at 55 °C.
Published example conditions should be assessed against each monomer and all protecting groups present in the synthesis sequence. For troubleshooting, contact the catalog team to connect with a technical expert. [R1, Example 9]
Read the 5′-CP application noteSingle-site gap walks, local backbone changes and preclinical study results

A single site and its adjacent backbone linkage

Kuroda et al. first walked single 5′-CP substitutions through ASO DNA gaps, then tested the substitutions with replacement of the immediately 5′-adjacent phosphorothioate (PS) linkage by a phosphodiester (PO) linkage. In the ASO1 paired walk, gap positions 1, 3, 4 and 5 reduced cytotoxicity and toxicity-associated transcripts without significantly reducing knockdown in that screen. [R2, Figure 6B]

At ASO1 gap position 3, the combined 5′-CP/PO design reduced late-onset neurotoxicity while maintaining Mapt knockdown in mouse hippocampus and lumbar cord. The study used a 38.4 nmol intracerebroventricular dose, four animals per group, and assessment at 21 days. Adding the PO linkage preserved knockdown more effectively than the corresponding 5′-CP/all-PS design in ASO1 and ASO4. [R2, Figure 6; supplementary Figure S24]

The result supports testing nucleoside placement and the neighboring linkage together, but remains sequence- and position-dependent; the authors did not observe mitigation of ASO2 acute-onset neurotoxicity from these gap modifications. [R2, Discussion]

A separate patent liver experiment

Patent constructNR3C1 mRNAALTAST
Parent ASO19100100
ASO2912.121.2
ASO3120.71.7
ASO4150.41.7
Male C57BL/6NCr mice, 20 mg/kg intravenously, assessed at 96 h. mRNA is normalized to saline = 100; each enzyme is normalized separately to parent ASO1 = 100. Modified constructs contain 5′-CP-T and local backbone changes. The patent ASO labels are unrelated to Kuroda’s labels. [R1, Figures 3–4]

A useful comparison for research

A matched set of parent ASO, 5′-CP substitution, PO-only variant and combined change can help assess 5′-CP incorporation and separate the two design variables. A preclinical screen may measure duplex binding, knockdown and tolerability separately.

scpBNA™ · Published evidence

Evaluate RNA affinity and nuclease-resistant wing chemistry

scpBNA T and MeC monomers provide bridged-sugar options at selected pyrimidine positions. Reported model oligonucleotides showed LNA-comparable RNA duplex stabilization and greater resistance to 3′-exonuclease degradation than LNA and unmodified DNA. [R3–R4]

In a 2025 mouse Scarb1 study, the all-scpBNA-wing construct LX-A2007 (T and MeC, all-PS backbone) retained substantial target knockdown and showed lower plasma AST than the LNA-wing reference LX-A1656. [R5, Figure 1]

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scpBNA™ scaffold
Read the scpBNA technical noteRNA duplex measurements, terminal stability, coupling and MeC handling considerations

scpBNA is a 2′-O,4′-C-spirocyclopropylene bridged nucleic acid. Published model-oligonucleotide experiments assess RNA affinity and terminal nuclease resistance as distinct properties. [R3–R4]

RNA affinity in model constructs

ConstructRNA duplex TmCorresponding LNA Tm
Unmodified reference ON149 °C—
Two scpBNA-T residues, ON5a60 °C61 °C
Two scpBNA-MeC residues, ON4a61 °C61 °C
PTEN-derived 14-mer; 4 µM each strand, 10 mM phosphate, pH 7.2, 10 mM NaCl; three measurements. Horiba et al. report rounded increases of +5 °C per T modification and +6 °C per MeC modification. The MeC comparison also includes methylation relative to natural C. [R4, Table 3]

Terminal stability

A technical report describes a terminal scpBNA-T model without PS linkages that retained more than 80% intact oligonucleotide after 60 minutes of exonuclease exposure, with resistance equal to or slightly better than a single-PS comparator. In the foundational patent’s separate assay, combined 10-mer and 9-mer material remained at 60% or more after 80 minutes, while the unmodified DNA-thymidine and LNA samples were nearly degraded by 20 minutes. [R6, Figure 2; R3, Example 5]

Published synthesis precedents

ParameterPublished example conditions
Scale and modified couplingPublished examples at 0.2, 1 and 10 µmol used 8-, 10- and 30-minute modified coupling, respectively. [R3–R5]
ActivatorActivator 42 in the patent and Kawanobe study; ETT in Horiba et al. [R3–R5]
Amidite solution0.1 M amidite in anhydrous acetonitrile. [R3; R5]
MeC solubilityFor a 0.1 M MeC solution, acetonitrile/THF 3:1 or acetonitrile/dichloromethane 1:1 has been used. [R6]
Cleavage and base deprotectionConcentrated ammonium hydroxide, 55 °C for 12 h. [R4; R6]
MeC(Bz) deprotection — proposed guidanceAvoid AMA (ammonium hydroxide/methylamine) with MeC(Bz) to limit an N4-methylated side product (M+14).
Assess these published examples against the synthesis scale, sequence and protecting groups in use. For troubleshooting, contact the catalog team to connect with a technical expert.
Read the scpBNA application notePublished T and MeC wing designs, backbone choices and activity/tolerability

All-PS scpBNA and LNA wing comparison

In a patent Pten experiment, an all-PS scpBNA-wing gapmer and its LNA comparator gave approximately 60–70% target suppression. The patent describes AST/ALT values for the scpBNA design at approximately half the LNA values. Male mice received 35 mg/kg intraperitoneally, with four animals per group and assessment at 72 h. [R3, Example 7]

Kawanobe 2025: all-scpBNA wings and mixed-chemistry designs

Kawanobe et al. compared Scarb1 gapmers with a ten-nucleotide DNA gap. The all-scpBNA construct LX-A2007 has three T/MeC residues in each wing and an all-PS backbone. Figure 1 compares this design with the LNA reference LX-A1656 and the AmNA-containing reference LX-A2001. [R5, Figure 1B]

Wing design / constructScarb1 mRNA % of vehiclePlasma AST IU/L
LNA; LX-A1656<5%≈2,200
AmNA + terminal DNA C; LX-A2001≈5%≈600
All-scpBNA; LX-A2007≈15%≈350
Approximate bar heights estimated from Figure 1D/E; these are not reported raw values. Knockdown: one 30 mg/kg subcutaneous dose, day-7 assessment, n = 3 or 6. AST: three 30 mg/kg subcutaneous doses on days 0, 2 and 4, day-7 assessment, n = 6. The two endpoints use different dosing regimens. [R5, Figure 1]

The all-scpBNA-wing construct LX-A2007 retained substantial Scarb1 knockdown with lower AST than the LNA reference LX-A1656 and the AmNA-containing reference LX-A2001. Further liver assessments examined mixed AmNA/scpBNA wings with two intra-wing PO linkages. The combined design reduced ALT, AST, total-bile-acid elevations and selected liver lesions, although residual lesions remained. [R5, Figures 1–3]

The combined AmNA/scpBNA/PO construct LX-A3928 showed approximately 1.5-fold weaker on-target knockdown activity and 2.5-fold improvement in the AST dose-response comparison versus the LNA/PS reference. These findings reflect the combined architecture. [R5, Results and supplementary Figure S3]

What this adds to the design toolkit

Evaluate T and MeC terminal and wing substitutions with selected PO and/or PS backbone linkages; assess RNA affinity, nuclease resistance, target knockdown and tolerability.

Sources and references (6)
  1. [R1] Obika et al. 5′-Modified Nucleoside and Nucleotide Using Same. US20220372060A1 (2022). Example 9: incorporation; Table 44: duplexes; Examples 11–12: nuclease and RNase H; Figures 3–4: liver experiment.

    https://patents.google.com/patent/US20220372060A1/en

  2. [R2] Kuroda et al. Unraveling and controlling late-onset neurotoxicity of antisense oligonucleotides through strategic chemical modifications. Molecular Therapy: Nucleic Acids 36, 102692 (2025). Figures 4–7 and supplementary Figures S19–S26.

    https://doi.org/10.1016/j.omtn.2025.102692

  3. [R3] Obika et al. Crosslinked Nucleoside and Nucleotide. US9611479B2 (2017). Examples 2 and 5: incorporation and stability; Example 7: Pten study.

    https://patents.google.com/patent/US9611479B2/en

  4. [R4] Horiba, Yamaguchi and Obika. Synthesis of scpBNA-mC, -A, and -G Monomers and Evaluation of the Binding Affinities of scpBNA-Modified Oligonucleotides toward Complementary ssRNA and ssDNA. Journal of Organic Chemistry 81, 11000–11008 (2016). Table 3 and synthesis/experimental sections.

    https://doi.org/10.1021/acs.joc.6b02036

  5. [R5] Kawanobe et al. Hepatotoxicity Reduction Profiles of Antisense Oligonucleotides Containing Amido-Bridged Nucleic Acid and 2′-O,4′-C-Spirocyclopropylene Bridged Nucleic Acid. Nucleic Acid Therapeutics 35, 114–124 (2025). Figure 1B: positions; Figures 1–3: activity and liver findings; Materials and Methods: synthesis.

    https://doi.org/10.1089/nat.2024.0047

  6. [R6] Shrestha and Kajino. Spirocyclopropylene bridged nucleic acid phosphoramidites. The Glen Report 36.2, 2–3 (2024). Luxna-authored technical report. Figure 2 and synthesis section.

    https://www.glenresearch.com/reports/gr36-21

Product selection and procurement

Specialized chemistry through WuXi TIDES

Source these six research-use amidites through the WuXi TIDES catalog. Contact our catalog team for product selection, current specifications, available documentation, availability and lead times.

For a quotation, send your catalog IDs, pack sizes, containers, number of packs and ship-to country to tides_catalog@wuxiapptec.com.

For uses beyond the permitted research-use scope, contact us to facilitate a referral to Summit Pharmaceuticals International.

Questions before you order

Where do I choose the pack and container?
Choose a 1 g, 2 g or 5 g pack and a container on the product card, then add it to your quote. The quote request carries your selected SKU, container and quantity. You can also browse the WuXi TIDES Online Shop; online ordering requires a registered account.
Can I request more than 10 g of one product?
Yes, you may request it for review. Quantities above 10 g of an individual product per order require Summit Pharmaceuticals International’s prior written approval. Count all packs and containers of that product together.
How do I select synthesis conditions?
For scpBNA, consider a 10-minute modified coupling cycle with 0.1 M amidite and Activator 42 or ETT as a starting point for 1 µmol synthesis. Published examples use longer coupling at 10 µmol. [R3–R5] For 5′-CP, consider four 240-second coupling cycles for the modified amidite and the next nucleotide, with 200-second capping and two 120-second deblocking cycles. [R1] Check the complete protecting-group set before selecting deprotection conditions. For troubleshooting, contact the catalog team to connect with a technical expert.
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