SCHEMBL805045

SCHEMBL805045

Cc1nc2ncccc2[nH]1

nearest known ligand 0.60

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
NUDT1 P36639 1/20 0.60
AURKA O14965 6/20 0.54
METAP1 P53582 2/20 0.53
METAP2 P50579 1/20 0.53
HPGD P15428 2/20 0.50
SMN1; SMN2 Q16637 2/20 0.50
NPC1 O15118 1/20 0.50
RAB9A P51151 1/20 0.50
PDE5A O76074 5/20 0.49
TP53 P04637 1/20 0.46
PDE2A O00408 1/20 0.44
PDE4A P27815 1/20 0.44
PDE4B Q07343 1/20 0.44
PDE4C Q08493 1/20 0.44
PDE4D Q08499 1/20 0.44

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
SCHEMBL9215893 0.79 AURKA (0.58) NUDT1AURKAMETAP1METAP2HPGD
SCHEMBL1170747 0.78 METAP1 (0.72) NUDT1AURKAMETAP1METAP2PDE5A
SCHEMBL14765145 0.77 NUDT1 (0.53) NUDT1AURKAMETAP1METAP2HPGD
SCHEMBL239645 0.77 NUDT1 (0.62) NUDT1AURKAMETAP1METAP2HPGD
SCHEMBL31490802 0.77 NUDT1 (0.62) NUDT1AURKAMETAP1METAP2HPGD
SCHEMBL24520478 0.75 NUDT1 (0.60) NUDT1AURKAMETAP1METAP2HPGD
SCHEMBL1427745 0.75 NUDT1 (0.60) NUDT1AURKAMETAP1METAP2HPGD
SCHEMBL21389521 0.75 NUDT1 (0.60) NUDT1AURKAMETAP1METAP2HPGD
SCHEMBL323981 0.75 NUDT1 (0.60) NUDT1AURKAMETAP1METAP2HPGD
SCHEMBL6962055 0.75 NUDT1 (0.60) NUDT1AURKAMETAP1METAP2HPGD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-120025352-A Condensed heterocyclic compound, pharmaceutical composition and application thereof 北京康辰药业股份有限公司 2025-05-23 CN claimed
CN-113387946-B Method for synthesizing 2-phenyl-3-arylamine methylimidazole pyridine derivative by using ultrasonic assistance in multiple components 衡阳师范学院 2023-08-01 CN claimed
CN-112143487-A Mesoporous silicon fluorescent probe for detecting heavy metal ions in cosmetics 高伟健 2020-12-29 CN claimed
US-20250230157-A1 AZABENZIMIDAZOLES AND THEIR USE AS AMPA RECEPTOR MODULATORS RAPPORT THERAPEUTICS, INC. 2025-07-17 US disclosed
CN-118488954-A Pyrrolo [2,1-F ] [1,2,4] triazine derivatives as DYRK1A inhibitors 拜斯丽治疗有限公司 2024-08-13 CN disclosed
WO-2024003259-A1 TEAD INHIBITORS BAYER AKTIENGESELLSCHAFT (DE) 2024-01-04 WO disclosed
US-11845762-B2 Compound functioning as bromodomain protein inhibitor, and composition BETTA PHARMACEUTICALS CO., LTD. (CN) 2023-12-19 US disclosed
US-20230390385-A1 Compositions and Methods for Prevention and Treatment of Immune Complex Disease COWAN FRED M (US) 2023-12-07 US disclosed
US-20230365524-A1 2,4,5-TRISUBSTITUTED 1,2,4-TRIAZOLONES USEFUL AS INHIBITORS OF DHODH BAYER AKTIENGESELLSCHAFT (DE) 2023-11-16 US disclosed
US-20230365524-A1 2,4,5-TRISUBSTITUTED 1,2,4-TRIAZOLONES USEFUL AS INHIBITORS OF DHODH BAYER AKTIENGESELLSCHAFT (DE) 2023-11-16 US disclosed
US-20230357239-A1 PYRIDO[2,3-D]PYRIMIDIN-4-AMINES AS SOS1 INHIBITORS BAYER AKTIENGESELLSCHAFT (DE) 2023-11-09 US disclosed
US-5359073-A Substituted-phenyl (N,N'-cycloalkyl/alkyl carboxamide)-1H/3H-imidazo[4,5-b]pyridine compounds as PAF antagonists G. D. SEARLE & CO. (US) 1994-10-25 US disclosed
WO-1994021255-A1 SIX-MEMBERED RING FUSED IMIDAZOLES SUBSTITUTED WITH PHENOXYPHENYLACETIC ACID DERIVATIVES MERCK & CO., INC. (US) 1994-09-29 WO disclosed
WO-1994017063-A1 N,N'-CYCLOALKYL/ALKYL CARBOXAMIDE 4H-IMIDAZO[4,5-b]PYRIDINE COMPOUNDS AS PAF ANTAGONISTS G.D. SEARLE & CO. (US) 1994-08-04 WO disclosed
US-5334598-A Have endothelin antagonist activity; useful in treating cardiovascular disorders, hypertension, inflammatory diseases and asthma MERCK & CO., INC. (US) 1994-08-02 US disclosed
WO-1994012500-A1 SUBSTITUTED-PHENYL(N,N'-CYCLOALKYL/ALKYL CARBOXAMIDE)-1H/3H-IMIDAZO[4,5-b]PYRIDINE COMPOUNDS AS PAF ANTAGONISTS G.D. SEARLE & CO. (US) 1994-06-09 WO disclosed
US-5262426-A Treatment of cardiovascular disorders, antiinflammatory agents G. D. SEARLE & CO. (US) 1993-11-16 US disclosed
US-5180724-A Platelet activating factor BRITISH BIO-TECHNOLOGY LIMITED (GB) 1993-01-19 US disclosed
WO-1992018503-A1 IMIDAZO (4,5-c)PYRIDO DERIVATIVES, PROCESS AND INTERMEDIATES FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM BRITISH BIO-TECHNOLOGY LIMITED (GB) 1992-10-29 WO disclosed
EP-0434038-A1 Fused imidazole derivatives, their production and use Takeda Chemical Industries, Ltd. (JP) 1991-06-26 EP 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 (4 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-20230357239-A1 PYRIDO[2,3-D]PYRIMIDIN-4-AMINES AS SOS1 INHIBITORS SOS1, PPM1D, SOS2 NUDT1 17/4885AURKA 1562/4885METAP1 1203/4885
US-11845762-B2 Compound functioning as bromodomain protein inhibitor, and composition BRD4, BRD1, BRD2 NUDT1 3392/4885AURKA 832/4885METAP1 3041/4885
US-20250230157-A1 AZABENZIMIDAZOLES AND THEIR USE AS AMPA RECEPTOR MODULATORS GRIN1, GRIN2B, GRIN3A NUDT1 1382/4885AURKA 744/4885METAP1 4243/4885
US-20230365524-A1 2,4,5-TRISUBSTITUTED 1,2,4-TRIAZOLONES USEFUL AS INHIBITORS OF DHODH DHODH, DHPS, DPYD NUDT1 205/4885AURKA 3407/4885METAP1 4307/4885

“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.