SCHEMBL3163036

SCHEMBL3163036

Nc1ncnc2c1ncn2[C@@H]1O[C@H](COP(=O)(O)OP(=O)(O)OP(=O)(O)O)CC1O

nearest known ligand 0.75

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
▸ P2RX1 P51575 4/20 0.70
▸ P2RX3 P56373 4/20 0.70
▸ P2RX2 Q9UBL9 2/20 0.70
▸ P2RY1 P47900 6/20 0.67
▸ P2RX4 Q99571 3/20 0.67
▸ P2RY2 P41231 2/20 0.67
▸ SRC P12931 1/20 0.67
▸ ALDH1A1 P00352 1/20 0.67
▸ SMN1; SMN2 Q16637 1/20 0.67
▸ RNASEL Q05823 1/20 0.65
▸ MACROD2 A1Z1Q3 1/20 0.63
▸ SIRT6 Q8N6T7 1/20 0.63
▸ MACROD1 Q9BQ69 1/20 0.63
▸ TRPM2 O94759 1/20 0.63
▸ PARG Q86W56 1/20 0.61

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
SCHEMBL20419143 1.00 P2RX1 (0.70) P2RX1P2RX3P2RX2P2RY1P2RX4
SCHEMBL29476737 1.00 P2RX1 (0.70) P2RX1P2RX3P2RX2P2RY1P2RX4
SCHEMBL19493160 1.00 P2RX1 (0.70) P2RX1P2RX3P2RX2P2RY1P2RX4
SCHEMBL29476738 1.00 P2RX1 (0.70) P2RX1P2RX3P2RX2P2RY1P2RX4
SCHEMBL250252 1.00 P2RX1 (0.70) P2RX1P2RX3P2RX2P2RY1P2RX4
SCHEMBL23982340 1.00 P2RX1 (0.70) P2RX1P2RX3P2RX2P2RY1P2RX4
SCHEMBL12932304 1.00 P2RX1 (0.70) P2RX1P2RX3P2RX2P2RY1P2RX4
SCHEMBL250251 1.00 P2RX1 (0.70) P2RX1P2RX3P2RX2P2RY1P2RX4
SCHEMBL23856115 0.99 P2RX1 (0.69) P2RX1P2RX3P2RX2P2RY1P2RX4
SCHEMBL22498804 0.99 P2RX1 (0.68) P2RX1P2RX3P2RX2P2RY1P2RX4

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 65 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10144972-B2 Composition for hot-start reverse transcription reaction or hot-start reverse transcription polymerase chain reaction BIONEER CORPORATION (KR) 2018-12-04 — — US claimed
EP-2824189-B1 COMPOSITION FOR HOT-START REVERSE TRANSCRIPTION REACTION OR HOT-START REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION BIONEER CORP (KR) 2018-01-31 — — EP claimed
EP-2837696-B1 HIGH-SENSITIVITY NUCLEIC ACID PREPARATION METHODS FOR THE DETECTION OF NUCLEIC ACID BY NUCLEIC ACID POLYMERASE BIONEER CORP (KR) 2018-01-31 — — EP claimed
US-20150072351-A1 HIGH-SENSITIVITY NUCLEIC ACID PREPARATION METHODS FOR THE DETECTION OF NUCLEIC ACID BY NUCLEIC ACID POLYMERASE BIONEER CORPORATION (KR) 2015-03-12 — — US claimed
EP-2837696-A2 METHOD FOR PREPARING A NUCLEIC ACID WITH HIGH PRECISION USED IN DETECTING A NUCLEIC ACID WITH A NUCLEIC ACID POLYMERASE Bioneer Corporation (KR) 2015-02-18 — — EP claimed
US-20150044683-A1 COMPOSITION FOR HOT-START REVERSE TRANSCRIPTION REACTION OR HOT-START REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION BIONEER CORPORATION (KR) 2015-02-12 — — US claimed
EP-2824189-A1 COMPOSITION FOR HOT-START REVERSE TRANSCRIPTION REACTION OR HOT-START REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION Bioneer Corporation (KR) 2015-01-14 — — EP claimed
US-4708935-A (2-5')-Oligo (3'-deoxyadenylate) and derivatives thereof RESEARCH CORPORATION (US) 1987-11-24 — — US claimed
US-20250163096-A1 2' AND/OR 5' AMINO-ACID ESTER PHOSPHORAMIDATE 3'-DEOXY ADENOSINE DERIVATIVES AS ANTI-CANCER COMPOUNDS NuCana plc (GB) 2025-05-22 — — US disclosed
US-12054510-B2 2′ and/or 5′ amino-acid ester phosphoramidate 3′-deoxy adenosine derivatives as anti-cancer compounds NuCana plc (GB) 2024-08-06 — — US disclosed
US-20220306675-A1 2' AND/OR 5' AMINO-ACID ESTER PHOSPHORAMIDATE 3'-DEOXY ADENOSINE DERIVATIVES AS ANTI-CANCER COMPOUNDS NuCana plc (GB) 2022-09-29 — — US disclosed
US-11352387-B2 2′ and/or 5′ amino-acid ester phosphoramidate 3′-deoxy adenosine derivatives as anti-cancer compounds NuCana plc (GB) 2022-06-07 — — US disclosed
US-20210338706-A1 ADENOSINE ANALOG AND ITS USE IN REGULATING THE CIRCADIAN CLOCK NATIONAL INSTITUTE OF BIOLOGICAL SCIENCES, BEIJING (CN) 2021-11-04 — — US disclosed
EP-3683225-A1 NEW 2' AND/OR 5' AMINO-ACID ESTER PHOSPHORAMIDATE 3'-DEOXY ADENOSINE DERIVATIVES AS ANTI-CANCER COMPOUNDS Nucana PLC (GB) 2020-07-22 — — EP disclosed
WO-1991018115-A1 PROMOTER LIGATION ACTIVATED TRANSCRIPTION AMPLIFICATION OF NUCLEIC ACID SEQUENCES LIFE TECHNOLOGIES, INC. (US) 1991-11-28 — — WO disclosed
EP-0420872-A1 THERAPEUTIC USES OF 2',5'-OLIGOADENYLATE DERIVATIVES. UNIV TEMPLE (US) 1991-04-10 — — EP disclosed
US-4859768-A Derivatives of 2', 5'-oligoadenylate and antiviral uses thereof TEMPLE UNIVERSITY OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION (US) 1989-08-22 — — US disclosed
US-4708935-A (2-5')-Oligo (3'-deoxyadenylate) and derivatives thereof RESEARCH CORPORATION (US) 1987-11-24 — — US disclosed
US-4539313-A VIRICIDES RESEARCH CORPORATION (US) 1985-09-03 — — US disclosed
US-4464359-A VIRICIDES RESEARCH CORPORATION (US) 1984-08-07 — — US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (5 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20220306675-A1 2' AND/OR 5' AMINO-ACID ESTER PHOSPHORAMIDATE 3'-DEOXY ADENOSINE DERIVATIVES AS ANTI-CANCER COMPOUNDS MTAP, ADA, ADORA2A P2RX1 1355/4885P2RX3 1110/4885P2RX2 1248/4885
US-12054510-B2 2′ and/or 5′ amino-acid ester phosphoramidate 3′-deoxy adenosine derivatives as anti-cancer compounds MTAP, ADA, ADORA2A P2RX1 1384/4885P2RX3 1153/4885P2RX2 1293/4885
US-11352387-B2 2′ and/or 5′ amino-acid ester phosphoramidate 3′-deoxy adenosine derivatives as anti-cancer compounds MTAP, RNMT, ADA P2RX1 2019/4885P2RX3 1614/4885P2RX2 1840/4885
US-20210338706-A1 ADENOSINE ANALOG AND ITS USE IN REGULATING THE CIRCADIAN CLOCK PER2, CRY1, ADORA2A P2RX1 216/4885P2RX3 296/4885P2RX2 261/4885
US-20250163096-A1 2' AND/OR 5' AMINO-ACID ESTER PHOSPHORAMIDATE 3'-DEOXY ADENOSINE DERIVATIVES AS ANTI-CANCER COMPOUNDS MTAP, ADA, ADORA2A P2RX1 1355/4885P2RX3 1110/4885P2RX2 1248/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.

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