SCHEMBL1673251

SCHEMBL1673251

Nc1ncnc2c1ncn2CC(=O)O

nearest known ligand 0.70

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
EGFR P00533 3/20 0.70
ALDH1A1 P00352 1/20 0.65
ADORA2A P29274 8/20 0.62
ADORA1 P30542 4/20 0.62
PI4KA P42356 3/20 0.61
PI4K2B Q8TCG2 3/20 0.61
PI4K2A Q9BTU6 3/20 0.61
PI4KB Q9UBF8 3/20 0.61
SRC P12931 1/20 0.59
KDR P35968 1/20 0.59
ADORA2B P29275 1/20 0.58
ADCY5 O95622 1/20 0.57
AHCY P23526 5/20 0.56

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
SCHEMBL17165347 0.87 EGFR (0.66) EGFRALDH1A1ADORA2AADORA1PI4KA
SCHEMBL27713663 0.86 EGFR (0.64) EGFRALDH1A1ADORA2AADORA1PI4KA
SCHEMBL983769 0.84 ADORA2A (0.68) EGFRALDH1A1ADORA2AADORA1PI4KA
SCHEMBL7199253 0.84 ADORA2A (0.62) EGFRALDH1A1ADORA2AADORA1PI4KA
SCHEMBL455646 0.82 P2RX7 (0.49) EGFRALDH1A1ADORA2AADORA1PI4KA
SCHEMBL17297723 0.82 ADCY5 (0.74) EGFRALDH1A1ADORA2AADORA1PI4KA
SCHEMBL6694591 0.82 EGFR (0.60) EGFRALDH1A1ADORA2AADORA1PI4KA
Acetic Acid SCHEMBL4107415 0.81 ADORA2A (0.82) EGFRALDH1A1ADORA2AADORA1PI4KA
SCHEMBL6045746 0.81 ADCY5 (0.74) EGFRALDH1A1ADORA2AADORA1PI4KA
SCHEMBL23885424 0.81 P2RX7 (0.66) EGFRALDH1A1KDR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20190262794-A1 SUBSTRATES, SYSTEMS, AND METHODS FOR NUCLEIC ACID ARRAY SYNTHESIS VIBRANT HOLDINGS, LLC 2019-08-29 US claimed
EP-3402897-A1 SUBSTRATES, SYSTEMS, AND METHODS FOR NUCLEIC ACID ARRAY SYNTHESIS Vibrant Holdings, LLC (US) 2018-11-21 EP claimed
WO-2017117292-A1 SUBSTRATES, SYSTEMS, AND METHODS FOR NUCLEIC ACID ARRAY SYNTHESIS VIBRANT HOLDINGS, LLC (US) 2017-07-06 WO claimed
CN-101157703-A Adenine bisphosphonate and preparation method thereof and application in pharmaceutical preparations UNIV HEBEI MEDICAL (CN) 2008-04-09 CN claimed
EP-0792283-A1 SYNTHESIS OF PEPTIDE NUCLEIC ACIDS (PNAs) AND ANALOGUES VIA SUBMONOMER APPROACH CHIRON CORPORATION (US) 1997-09-03 EP claimed
WO-1996015143-A1 SYNTHESIS OF PEPTIDE NUCLEIC ACIDS (PNAs) AND ANALOGUES VIA SUBMONOMER APPROACH CHIRON CORPORATION (US) 1996-05-23 WO claimed
US-20230294064-A1 SUBSTRATES, SYSTEMS, AND METHODS FOR NUCLEIC ACID ARRAY SYNTHESIS VIBRANT HOLDINGS, LLC 2023-09-21 US disclosed
US-20230159536-A1 PYRROLOPYRIMIDINE AMINES AS COMPLEMENT INHIBITORS WILMINGTON TRUST, NATIONAL ASSOCIATION 2023-05-25 US disclosed
US-20230159536-A1 PYRROLOPYRIMIDINE AMINES AS COMPLEMENT INHIBITORS WILMINGTON TRUST, NATIONAL ASSOCIATION 2023-05-25 US disclosed
US-20230159536-A1 PYRROLOPYRIMIDINE AMINES AS COMPLEMENT INHIBITORS WILMINGTON TRUST, NATIONAL ASSOCIATION 2023-05-25 US disclosed
EP-4125914-A1 PYRROLOPYRIMIDINE AMINES AS COMPLEMENT INHIBITORS Biocryst Pharmaceuticals, Inc. (US) 2023-02-08 EP disclosed
CN-115427044-A Pyrrolopyrimidines as complement inhibitors 拜奥克里斯特制药公司 2022-12-02 CN disclosed
US-11311520-B2 Substituted dihydroimidazopyridinediones as MKNK1 and MKNK2 inhibitors BAYER PHARMA AKTIENGESELLSCHAFT (DE) 2022-04-26 US disclosed
EP-0639607-B1 Method and apparatus for degradation and sequencing of polymers which sequentially eliminate terminal residues PERSEPTIVE BIOSYSTEMS INC (US) 1998-01-07 EP disclosed
EP-0792283-A1 SYNTHESIS OF PEPTIDE NUCLEIC ACIDS (PNAs) AND ANALOGUES VIA SUBMONOMER APPROACH CHIRON CORPORATION (US) 1997-09-03 EP disclosed
US-5527675-A Method for degradation and sequencing of polymers which sequentially eliminate terminal residues MILLIPORE CORPORATION (US) 1996-06-18 US disclosed
WO-1996015143-A1 SYNTHESIS OF PEPTIDE NUCLEIC ACIDS (PNAs) AND ANALOGUES VIA SUBMONOMER APPROACH CHIRON CORPORATION (US) 1996-05-23 WO disclosed
EP-0639607-A2 Method and apparatus for degradation and sequencing of polymers which sequentially eliminate terminal residues PERSEPTIVE BIOSYSTEMS, INC. (US) 1995-02-22 EP disclosed
EP-0586474-A1 PEPTIDE NUCLEIC ACIDS BUCHARDT, Ole (DK) 1994-03-16 EP disclosed
WO-1992020702-A1 PEPTIDE NUCLEIC ACIDS BUCHARDT OLE (DK) 1992-11-26 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-20230159536-A1 PYRROLOPYRIMIDINE AMINES AS COMPLEMENT INHIBITORS C5, C9, C1QBP EGFR 2721/4885ALDH1A1 1325/4885ADORA2A 1283/4885
US-11311520-B2 Substituted dihydroimidazopyridinediones as MKNK1 and MKNK2 inhibitors MKNK1, MKNK2, MAP4K5 EGFR 2624/4885ALDH1A1 2000/4885ADORA2A 4316/4885

“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.