SCHEMBL4581742

SCHEMBL4581742

COCCOC[C@H]1O[C@@H](n2cnc3c(N)ncnc32)[C@H](O)[C@@H]1O

nearest known ligand 0.70

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ P2RY1 P47900 4/20 0.70
▸ SMN1; SMN2 Q16637 3/20 0.70
▸ P2RY2 P41231 3/20 0.70
▸ ADORA1 P30542 3/20 0.70
▸ SRC P12931 2/20 0.70
▸ DNPH1 O43598 1/20 0.70
▸ PRKAB2 O43741 1/20 0.70
▸ TRPM2 O94759 1/20 0.70
▸ LDHA P00338 1/20 0.70
▸ ADRB2 P07550 1/20 0.70
▸ FBP1 P09467 1/20 0.70
▸ PRKAG1 P54619 1/20 0.70
▸ PRKAA2 P54646 1/20 0.70
▸ PDE4D Q08499 1/20 0.70
▸ KCNH2 Q12809 1/20 0.70
▸ PRKAA1 Q13131 1/20 0.70
▸ PDE3A Q14432 1/20 0.70
▸ TAS1R3 Q7RTX0 1/20 0.70
▸ TAS1R1 Q7RTX1 1/20 0.70
▸ P2RY11 Q96G91 1/20 0.70

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
SCHEMBL8328542 0.95 ADORA1 (0.74) P2RY1SMN1; SMN2P2RY2ADORA1SRC
SCHEMBL8164443 0.91 P2RY1 (0.68) P2RY1SMN1; SMN2P2RY2ADORA1SRC
SCHEMBL2534140 0.91 EHMT1 (0.70) P2RY1SMN1; SMN2P2RY2ADORA1SRC
SCHEMBL384075 0.90 ADORA1 (0.74) P2RY1SMN1; SMN2P2RY2ADORA1SRC
SCHEMBL15338536 0.90 ADORA1 (0.74) P2RY1SMN1; SMN2P2RY2ADORA1SRC
SCHEMBL15926827 0.90 ADORA1 (0.74) P2RY1SMN1; SMN2P2RY2ADORA1SRC
SCHEMBL41361 0.90 ADORA1 (0.74) P2RY1SMN1; SMN2P2RY2ADORA1SRC
SCHEMBL15788449 0.90 ADORA1 (0.74) P2RY1SMN1; SMN2P2RY2ADORA1SRC
SCHEMBL15338502 0.90 ADORA1 (0.74) P2RY1SMN1; SMN2P2RY2ADORA1SRC
SCHEMBL29936504 0.90 ADORA1 (0.74) P2RY1SMN1; SMN2P2RY2ADORA1SRC

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240229036-A9 NUCLEIC ACID MEDICINE EXPRESSING SPLICING VARIANT OF MYOSTATIN KNC LABORATORIES CO., LTD. (JP) 2024-07-11 — — US disclosed
WO-2024137993-A2 ENGINEERED GUIDE RNAS AND POLYNUCLEOTIDES SHAPE THERAPEUTICS INC. (US) 2024-06-27 — — WO disclosed
US-20240200061-A1 TRANSTHYRETIN (TTR) iRNA COMPOSITIONS AND METHODS OF USE THEREOF FOR TREATING OR PREVENTING TTR-ASSOCIATED OCULAR DISEASES ALNYLAM PHARMACEUTICALS, INC. 2024-06-20 — — US disclosed
EP-4384617-A1 FACTOR XII (F12) IRNA COMPOSITIONS AND METHODS OF USE THEREOF Alnylam Pharmaceuticals, Inc. (US) 2024-06-19 — — EP disclosed
EP-4381071-A1 IRNA COMPOSITIONS AND METHODS FOR SILENCING ANGIOTENSINOGEN (AGT) Alnylam Pharmaceuticals, Inc. (US) 2024-06-12 — — EP disclosed
EP-4381067-A1 TRANSTHYRETIN (TTR) IRNA COMPOSITIONS AND METHODS OF USE THEREOF Alnylam Pharmaceuticals, Inc. (US) 2024-06-12 — — EP disclosed
EP-4377458-A1 3-HYDROXY-3-METHYLGLUTARYL-COA REDUCTASE (HMGCR) IRNA COMPOSITIONS AND METHODS OF USE THEREOF Alnylam Pharmaceuticals, Inc. (US) 2024-06-05 — — EP disclosed
EP-4373933-A1 BETA-CATENIN (CTNNB1) IRNA COMPOSITIONS AND METHODS OF USE THEREOF Alnylam Pharmaceuticals, Inc. (US) 2024-05-29 — — EP disclosed
US-20240132893-A1 NUCLEIC ACID MEDICINE EXPRESSING SPLICING VARIANT OF MYOSTATIN KNC LABORATORIES CO., LTD. (JP) 2024-04-25 — — US disclosed
EP-4351541-A2 COMPOSITIONS AND METHODS FOR TREATING OR PREVENTING STARGARDT'S DISEASE AND/OR RETINAL BINDING PROTEIN 4 (RBP4)-ASSOCIATED DISORDERS Alnylam Pharmaceuticals, Inc. (US) 2024-04-17 — — EP disclosed
WO-2017019660-A1 XANTHINE DEHYDROGENASE (XDH) IRNA COMPOSITIONS AND METHODS OF USE THEREOF ALNYLAM PHARMACEUTICALS, INC. (US) 2017-02-02 — — WO disclosed
EP-2970974-A2 COMPLEMENT COMPONENT C5 IRNA COMPOSITIONS AND METHODS OF USE THEREOF Alnylam Pharmaceuticals, Inc. (US) 2016-01-20 — — EP disclosed
WO-2014160129-A2 COMPLEMENT COMPONENT C5 IRNA COMPOSITIONS AND METHODS OF USE THEREOF ALNYLAM PHARMACEUTICALS, INC. (US) 2014-10-02 — — WO disclosed
US-7371852-B2 Alkyl-linked nucleotide compositions SERENEX, INC. (US) 2008-05-13 — — US disclosed
EP-1585754-A2 ALKYL-LINKED NUCLEOTIDE COMPOSITIONS Serenex, Inc. (US) 2005-10-19 — — EP disclosed
US-20040215009-A1 Alkyl-linked nucleotide compositions SERENEX, INC. (US) 2004-10-28 — — US disclosed
US-6800751-B2 ALKYLATION OF 2'-HYDROXY GROUP OF RIBONUCLEOSIDE PROTECTED WITH INVENTIVE SILYLATING AGENTS IN PRESENCE OF EXCESS OF MILD HINDERED BASE MAY BE CARRIED OUT WITHOUT PROTECTING EXOCYCLIC AMINE AND OXO FUNCTIONALITIES OF NUCLEOBASES ISIS PHARMACEUTICALS, INC. 2004-10-05 — — US disclosed
WO-2004065566-A2 ALKYL-LINKED NUCLEOTIDE COMPOSITIONS SERENEX, INC. (US) 2004-08-05 — — WO disclosed
US-20030225262-A1 Reagent and process for protecting active groups IONIS PHARMACEUTICALS, INC. 2003-12-04 — — US disclosed
WO-2003087053-A2 REAGENT AND PROCESS FOR PROTECTING NUCLEOSIDE ACTIVE GROUPS ISIS PHARMACEUTICALS, INC. (US) 2003-10-23 — — WO 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 (2 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-20030225262-A1 Reagent and process for protecting active groups TRDMT1, SBDS, DIMT1 P2RY1 4547/4885SMN1; SMN2 229/4885P2RY2 4172/4885
US-20040215009-A1 Alkyl-linked nucleotide compositions NT5C3B, NUDT1, NT5C2 P2RY1 446/4885SMN1; SMN2 2062/4885P2RY2 666/4885

“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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