SCHEMBL669007

SCHEMBL669007

C=CCn1c(N)nc2nc[nH]c2c1=O

nearest known ligand 0.61

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
▸ ADORA2B P29275 9/20 0.61
▸ ADORA2A P29274 9/20 0.61
▸ ADORA3 P0DMS8 1/20 0.56
▸ PDE4A P27815 6/20 0.54
▸ PDE4B Q07343 6/20 0.54
▸ PDE4C Q08493 6/20 0.54
▸ PDE4D Q08499 6/20 0.54
▸ CDK1 P06493 2/20 0.46
▸ CCNB1 P14635 2/20 0.46
▸ CCNA2 P20248 2/20 0.46
▸ CDK2 P24941 2/20 0.46
▸ CCNA1 P78396 2/20 0.46
▸ MGMT P16455 1/20 0.46
▸ PNP P00491 2/20 0.43
▸ DPP4 P27487 1/20 0.41
▸ PDPK1 O15530 1/20 0.39
▸ GDA Q9Y2T3 1/20 0.39

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
SCHEMBL1047660 0.82 PNP (0.45) ADORA2BADORA2APDE4APDE4BPDE4C
SCHEMBL874737 0.82 ADORA2A (0.56) ADORA2BADORA2AADORA3PDE4APDE4B
SCHEMBL28071828 0.82 PNP (0.45) ADORA2BADORA2APDE4APDE4BPDE4C
SCHEMBL9308358 0.81 ADORA2B (0.52) ADORA2BADORA2AADORA3PDE4APDE4B
SCHEMBL5667530 0.79 ADORA2A (0.61) ADORA2BADORA2AADORA3PDE4APDE4B
SCHEMBL3671339 0.79 DPP4 (0.44) ADORA2BADORA2AADORA3PDE4APDE4B
SCHEMBL667797 0.79 PDE4A (0.60) ADORA2BADORA2AADORA3PDE4APDE4B
SCHEMBL27842808 0.79 PDE4A (0.53) ADORA2BADORA2APDE4APDE4BPDE4C
SCHEMBL6265538 0.79 MGMT (0.47) ADORA2BADORA2APDE4APDE4BPDE4C
SCHEMBL29203683 0.79 PNP (0.45) ADORA2BADORA2AADORA3PDE4APDE4B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117795071-A Antisense oligonucleotides for preventing renal dysfunction caused by endothelial dysfunction through inhibition of ephrin-B2 马克斯·普朗克科学促进学会 2024-03-29 — — CN claimed
US-20210363172-A1 5'-CAP-TRINUCLEOTIDE- OR HIGHER OLIGONUCLEOTIDE COMPOUNDS AND THEIR USE IN STABILIZING RNA, EXPRESSING PROTEINS IN THERAPY BIONTECH RNA PHARMACEUTICALS GMBH (DE) 2021-11-25 — — US claimed
EP-3765477-A1 5'-CAP-TRINUCLEOTIDE- OR HIGHER OLIGONUCLEOTIDE COMPOUNDS AND THEIR USES IN STABILIZING RNA, EXPRESSING PROTEINS AND IN THERAPY BioNTech RNA Pharmaceuticals GmbH (DE) 2021-01-20 — — EP claimed
CN-112119084-A 5' -cap trinucleotide or higher oligonucleotide compounds and their use in RNA stabilization, protein expression and therapy 生物技术RNA制药有限公司 2020-12-22 — — CN claimed
EP-2370808-B2 ELECTROCHEMICAL GAS SENSORS WITH IONIC LIQUID ELECTROLYTE SYSTEMS MSA EUROPE GMBH (CH) 2020-07-22 — — EP claimed
CN-105377250-B Compositions and methods for combating antibacterial resistant bacteria 蓝莓疗法有限公司 2020-04-03 — — CN claimed
WO-2019175356-A1 5'-CAP-TRINUCLEOTIDE- OR HIGHER OLIGONUCLEOTIDE COMPOUNDS AND THEIR USES IN STABILIZING RNA, EXPRESSING PROTEINS AND IN THERAPY BIONTECH RNA PHARMACEUTICALS GMBH (DE) 2019-09-19 — — WO claimed
US-9909169-B2 Allele-specific amplification of nucleic acids using blocking oligonucleotides for wild type suppression ROCHE MOLECULAR SYSTEMS, INC. (US) 2018-03-06 — — US claimed
EP-2370808-B1 ELECTROCHEMICAL GAS SENSORS WITH IONIC LIQUID ELECTROLYTE SYSTEMS MSA EUROPE GMBH (CH) 2017-11-01 — — EP claimed
EP-3234180-A1 ALLELE-SPECIFIC AMPLIFICATION OF NUCLEIC ACIDS USING BLOCKING OLIGONUCLEOTIDES FOR WILD TYPE SUPPRESSION Roche Diagnostics GmbH (DE) 2017-10-25 — — EP claimed
US-20100099110-A1 Allele-Specific Amplification ROCHE MOLECULAR SYSTEMS, INC. (US) 2010-04-22 — — US claimed
EP-1117838-B1 A METHOD FOR ANALYZING POLYNUCLEOTIDES VARIAGENICS INC (US) 2009-05-13 — — EP claimed
CN-101115995-A Covalent tethering of functional groups to proteins and substrates therefor PROMEGA CORP (US) 2008-01-30 — — CN claimed
EP-1117838-A4 A METHOD FOR ANALYZING POLYNUCLEOTIDES VARIAGENICS INC (US) 2007-05-02 — — EP claimed
CN-1463292-A Method for analyzing polynucleotide VARY GENIX CORP (US) 2003-12-24 — — CN claimed
US-6566059-B1 Method for analyzing polynucleotides VARIAGENICS, INC. 2003-05-20 — — US claimed
JP-2002525129-A — — 2002-08-13 — — JP claimed
EP-1117838-A1 A METHOD FOR ANALYZING POLYNUCLEOTIDES Variagenics, Inc. (US) 2001-07-25 — — EP claimed
WO-2000018967-A1 A METHOD FOR ANALYZING POLYNUCLEOTIDES VARIAGENICS, INC. (US) 2000-04-06 — — WO claimed
EP-0625985-B1 METHOD AND RING-OPENED PURINE COMPOUNDS FOR LABELING POLYNUCLEOTIDES UNIV MIAMI (US) 1997-06-11 — — EP claimed

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-20210363172-A1 5'-CAP-TRINUCLEOTIDE- OR HIGHER OLIGONUCLEOTIDE COMPOUNDS AND THEIR USE IN STABILIZING RNA, EXPRESSING PROTEINS IN THERAPY RNMT, RNGTT, NSUN3 ADORA2B 2996/4885ADORA2A 1232/4885ADORA3 1937/4885
US-20100099110-A1 Allele-Specific Amplification RNGTT, HLA-C, POLL ADORA2B 482/4885ADORA2A 354/4885ADORA3 340/4885

“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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