SCHEMBL15698596

SCHEMBL15698596

[N-]=[N+]=N[C@@H]1[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O[C@H]1n1cnc2c(N)ncnc21

nearest known ligand 0.75

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ P2RX1 P51575 4/20 0.75
▸ P2RX3 P56373 4/20 0.75
▸ P2RX2 Q9UBL9 2/20 0.75
▸ P2RY1 P47900 7/20 0.73
▸ P2RY2 P41231 3/20 0.73
▸ ALDH1A1 P00352 3/20 0.73
▸ SRC P12931 2/20 0.73
▸ SMN1; SMN2 Q16637 2/20 0.73
▸ P2RX4 Q99571 2/20 0.73
▸ RNASEL Q05823 1/20 0.70
▸ HIF1A Q16665 1/20 0.69
▸ TRPM2 O94759 2/20 0.69
▸ MACROD2 A1Z1Q3 1/20 0.69
▸ SIRT6 Q8N6T7 1/20 0.69
▸ MACROD1 Q9BQ69 1/20 0.69
▸ DNPH1 O43598 1/20 0.65
▸ PRKAB2 O43741 1/20 0.65
▸ LDHA P00338 1/20 0.65
▸ ADRB2 P07550 1/20 0.65
▸ FBP1 P09467 1/20 0.65

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
SCHEMBL18771184 1.00 P2RX1 (0.75) P2RX1P2RX3P2RX2P2RY1P2RY2
SCHEMBL29750562 1.00 P2RX1 (0.75) P2RX1P2RX3P2RX2P2RY1P2RY2
SCHEMBL20820229 1.00 P2RX1 (0.75) P2RX1P2RX3P2RX2P2RY1P2RY2
SCHEMBL15703927 0.93 P2RY1 (0.73) P2RX1P2RX3P2RX2P2RY1P2RY2
SCHEMBL18771186 0.93 P2RY1 (0.73) P2RX1P2RX3P2RX2P2RY1P2RY2
SCHEMBL12961954 0.90 P2RX1 (0.78) P2RX1P2RX3P2RX2P2RY1P2RY2
SCHEMBL20820163 0.89 P2RY1 (0.63) P2RX1P2RX3P2RX2P2RY1P2RY2
SCHEMBL16081092 0.89 P2RY1 (0.63) P2RX1P2RX3P2RX2P2RY1P2RY2
Adenosine Triphosphate SCHEMBL4362224 0.88 P2RY1 (0.94) P2RX1P2RX3P2RX2P2RY1P2RY2
Adenosine Triphosphate SCHEMBL20550531 0.88 P2RY1 (0.94) P2RX1P2RX3P2RX2P2RY1P2RY2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20220145295-A1 ENZYMATIC RNA SYNTHESIS PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 2022-05-12 — — US claimed
EP-3864151-A2 ENZYMATIC RNA SYNTHESIS President and Fellows of Harvard College (US) 2021-08-18 — — EP claimed
US-20210052706-A1 COMPOSITIONS AND METHODS FOR FACILITATING DELIVERY OF SYNTHETIC NUCLEIC ACIDS TO CELLS TRANSLATE BIO MA, INC. (US) 2021-02-25 — — US claimed
EP-3737424-A1 COMPOSITIONS AND METHODS FOR FACILITATING DELIVERY OF SYNTHETIC NUCLEIC ACIDS TO CELLS Translate Bio MA, Inc. (US) 2020-11-18 — — EP claimed
US-20180311176-A1 NANOPARTICLE FORMULATIONS FOR DELIVERY OF NUCLEIC ACID COMPLEXES TRANSLATE BIO MA, INC. (US) 2018-11-01 — — US claimed
EP-3368089-A1 NANOPARTICLE FORMULATIONS FOR DELIVERY OF NUCLEIC ACID COMPLEXES TRANSLATE BIO MA, INC. (US) 2018-09-05 — — EP claimed
WO-2017075038-A1 NANOPARTICLE FORMULATIONS FOR DELIVERY OF NUCLEIC ACID COMPLEXES RANA THERAPEUTICS, INC. (US) 2017-05-04 — — WO claimed
EP-3033424-A1 COMPOSITIONS AND METHODS FOR MODULATING RNA Rana Therapeutics, Inc. (US) 2016-06-22 — — EP claimed
WO-2015023975-A1 COMPOSITIONS AND METHODS FOR MODULATING RNA RANA THERAPEUTICS, INC. (US) 2015-02-19 — — WO claimed
US-20140170689-A1 Modified Diguanylate Cyclase-Phosphodiesterase and Method for Enzymatic Production of Cyclic-diGMP THE RESEARCH FOUNDATION FOR THE STATE UNIVERSITY OF NEW YORK (US) 2014-06-19 — — US claimed
EP-2451980-B1 CHEMICALLY MODIFIED LIGASE COFACTORS, DONORS AND ACCEPTORS TRILINK BIOTECHNOLOGIES (US) 2014-05-21 — — EP claimed
US-8728725-B2 Chemically modified ligase cofactors, donors and acceptors TRILINK BIOTECHNOLOGIES (US) 2014-05-20 — — US claimed
US-20260138999-A1 REAGENTS AND THEIR USE FOR MODULAR ENANTIODIVERGENT SYNTHESIS OF C-P BONDS BRISTOL MYERS SQUIBB CO (US) 2026-05-21 — — US disclosed
US-12545900-B2 CGAS/DNCV-like nucleotidyltransferases and uses thereof DANA-FARBER CANCER INSTITUTE, INC. (US) 2026-02-10 — — US disclosed
US-12492217-B2 Reagents and their use for modular enantiodivergent synthesis of C—P bonds BRISTOL-MYERS SQUIBB COMPANY (US) 2025-12-09 — — US disclosed
US-20250360089-A1 NANOPARTICLE FORMULATIONS FOR DELIVERY OF NUCLEIC ACID COMPLEXES TRANSLATE BIO MA, INC. (US) 2025-11-27 — — US disclosed
WO-2014160484-A1 AMINO ACID PHOSPHORAMIDATE PRONUCLEOTIDES OF 2'-CYANO, AZIDO AND AMINO NUCLEOSIDES FOR THE TREATMENT OF HCV IDENIX PHARMACEUTICALS, INC. (US) 2014-10-02 — — WO disclosed
US-20140271547-A1 AMINO ACID PHOSPHORAMIDATE PRONUCLEOTIDES OF 2'-CYANO, AZIDO AND AMINO NUCLEOSIDES FOR THE TREATMENT OF HCV IDENIX PHARMACEUTICALS, INC. 2014-09-18 — — US disclosed
US-20140271547-A1 AMINO ACID PHOSPHORAMIDATE PRONUCLEOTIDES OF 2'-CYANO, AZIDO AND AMINO NUCLEOSIDES FOR THE TREATMENT OF HCV IDENIX PHARMACEUTICALS, INC. 2014-09-18 — — US disclosed
US-20140170689-A1 Modified Diguanylate Cyclase-Phosphodiesterase and Method for Enzymatic Production of Cyclic-diGMP THE RESEARCH FOUNDATION FOR THE STATE UNIVERSITY OF NEW YORK (US) 2014-06-19 — — 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 (7 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-20260138999-A1 REAGENTS AND THEIR USE FOR MODULAR ENANTIODIVERGENT SYNTHESIS OF C-P BONDS RNGTT, CDA, DCTD P2RX1 1240/4885P2RX3 1431/4885P2RX2 1490/4885
US-20180311176-A1 NANOPARTICLE FORMULATIONS FOR DELIVERY OF NUCLEIC ACID COMPLEXES DIS3, SYNCRIP, EXOSC5 P2RX1 4598/4885P2RX3 4577/4885P2RX2 4724/4885
US-20250360089-A1 NANOPARTICLE FORMULATIONS FOR DELIVERY OF NUCLEIC ACID COMPLEXES DIS3, SYNCRIP, EXOSC5 P2RX1 4598/4885P2RX3 4577/4885P2RX2 4724/4885
US-20210052706-A1 COMPOSITIONS AND METHODS FOR FACILITATING DELIVERY OF SYNTHETIC NUCLEIC ACIDS TO CELLS NSUN3, RNGTT, CSGALNACT1 P2RX1 4858/4885P2RX3 4846/4885P2RX2 4852/4885
US-20140271547-A1 AMINO ACID PHOSPHORAMIDATE PRONUCLEOTIDES OF 2'-CYANO, AZIDO AND AMINO NUCLEOSIDES FOR THE TREATMENT OF HCV PNP, RNGTT, NSUN2 P2RX1 84/4885P2RX3 144/4885P2RX2 185/4885
US-12492217-B2 Reagents and their use for modular enantiodivergent synthesis of C—P bonds PNKP, POLL, RNGTT P2RX1 2268/4885P2RX3 2326/4885P2RX2 2022/4885
US-12545900-B2 CGAS/DNCV-like nucleotidyltransferases and uses thereof NT5C2, NT5DC2, NTPCR P2RX1 223/4885P2RX3 304/4885P2RX2 156/4885

“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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