SCHEMBL278145

SCHEMBL278145

Nc1nccn2ccnc12

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 6)

geneUniProtsupporting neighboursconfidence
NUDT1 P36639 1/20 1.00
ADORA2A P29274 1/20 0.38
TLR7 Q9NYK1 12/20 0.37
L3MBTL1 Q9Y468 1/20 0.36
SMPD3 Q9NY59 1/20 0.34
AHCY P23526 1/20 0.34

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
SCHEMBL21082025 0.75 NUDT1 (0.59) NUDT1TLR7AHCY
SCHEMBL17505391 0.73 NUDT1 (0.57) NUDT1TLR7
SCHEMBL335977 0.73 NUDT1 (0.58) NUDT1ADORA2AL3MBTL1SMPD3
SCHEMBL15688262 0.72 NUDT1 (0.55) NUDT1ADORA2AL3MBTL1
SCHEMBL5477688 0.72 NUDT1 (0.55) NUDT1ADORA2AL3MBTL1
SCHEMBL14381039 0.72 NUDT1 (0.55) NUDT1ADORA2AL3MBTL1
SCHEMBL9080834 0.72 NUDT1 (0.55) NUDT1ADORA2ATLR7L3MBTL1
SCHEMBL5496407 0.72 NUDT1 (0.56) NUDT1SMPD3
Hydrochloric Acid SCHEMBL8374910 0.72 NUDT1 (0.56) NUDT1ADORA2AL3MBTL1SMPD3
SCHEMBL17505363 0.70 NUDT1 (0.54) NUDT1ADORA2AL3MBTL1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115667264-A Novel imidazo-pyrazine derivatives 豪夫迈·罗氏有限公司 2023-01-31 CN claimed
US-20090274626-A1 TARGETING TNF-alpha CONVERTING ENZYME(TACE)- DEPENDENT GROWTH FACTOR SHEDDING IN CANCER THERAPY THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2009-11-05 US claimed
WO-2007016597-A2 TARGETING TNF-ALPHA CONVERTING ENZYME (TACE)-DEPENDENT GROWTH FACTOR SHEDDING IN CANCER THERAPY THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2007-02-08 WO claimed
US-5028605-A Antispasmodic, bronchodilators, uterine relaxants, cardiac analeptics, neurosedatives L'UNIVERSITE DE MONTPELLIER I (FR) 1991-07-02 US claimed
US-12516065-B2 Tertiary alcohols as PI3K-γ inhibitors INCYTE CORPORATION (US) 2026-01-06 US disclosed
EP-4638454-A1 SUBSTITUTED IMIDAZO-BASED COMPOUNDS AS LIGAND DIRECTED DEGRADERS OF IRAK3 Celgene Corporation (US) 2025-10-29 EP disclosed
EP-4562012-A1 SUBSTITUTED IMIDAZOPYRAZINE COMPOUNDS AS LIGAND DIRECTED DEGRADERS OF IRAK3 CELGENE CORPORATION (US) 2025-06-04 EP disclosed
EP-4562013-A1 SUBSTITUTED IMIDAZOPYRAZINE COMPOUNDS AS IRAK3 BINDERS CELGENE CORPORATION (US) 2025-06-04 EP disclosed
CN-119894513-A Heterocycles as modulators of NSD activity 德州大学系统董事会 2025-04-25 CN disclosed
US-12263163-B2 Crystalline succinate salt of 6-(6-aminopyrazin-2-yl)-n-(4-(4-(oxetan-3-yl)piperazin-1-yl)phenyl)imidazo[1,2-a]pyrazin-8-amine as a Syk inhibitor Kronos Bio, Inc. (US) 2025-04-01 US disclosed
US-20240228498-A1 TERTIARY ALCOHOLS AS PI3K-y INHIBITORS INCYTE CORPORATION 2024-07-11 US disclosed
US-12030885-B2 Substituted imidazo[2,1-f][1,2,4]triazines as PI3K-gamma inhibitors INCYTE CORPORATION (US) 2024-07-09 US disclosed
US-20040067951-A1 6-aryl-imidazo[1,2-a] pyrazin-8-ylamines, method of making, and method of use thereof GILEAD CONNECTICUT, INC. 2004-04-08 US disclosed
WO-2004022562-A1 6-ARYL-IMIDAZO[1,2-a]PYRAZIN-8-YLAMINES, METHOD OF MAKING, AND METHOD OF USE THEREOF CELLULAR GENOMICS, INC. (US) 2004-03-18 WO disclosed
US-20030212073-A1 Imidazo[1,2-a]pyrazin-8-ylamines, method of making, and method of use thereof GILEAD CONNECTICUT, INC. 2003-11-13 US disclosed
US-20030212073-A1 Imidazo[1,2-a]pyrazin-8-ylamines, method of making, and method of use thereof GILEAD CONNECTICUT, INC. 2003-11-13 US disclosed
WO-2003089434-A2 IMIDAZO[1,2-a]PYRAZIN-8-YLAMINES METHOD OF MAKING AND METHOD OF USE THEREOF CELLULAR GENOMICS, INC. (US) 2003-10-30 WO disclosed
US-5028605-A Antispasmodic, bronchodilators, uterine relaxants, cardiac analeptics, neurosedatives L'UNIVERSITE DE MONTPELLIER I (FR) 1991-07-02 US disclosed
EP-0348392-A1 8-ALKYLAMINOIMIDAZO[1,2-A]PYRAZINES AND DERIVATIVES, THEIR PREPARATION AND THEIR APPLICATION IN THERAPY Université Montpellier I (FR) 1990-01-03 EP disclosed
WO-1988004298-A1 8-ALKYLAMINOIMIDAZO[1,2-A]PYRAZINES AND DERIVATIVES, THEIR PREPARATION AND THEIR APPLICATION IN THERAPY BYK GULDEN LOMBERG CHEMISCHE FABRIK GMBH (DE) 1988-06-16 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 (5 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-20040067951-A1 6-aryl-imidazo[1,2-a] pyrazin-8-ylamines, method of making, and method of use thereof MAP3K8, PRKACA, MAP3K1 NUDT1 995/4885ADORA2A 1225/4885TLR7 2271/4885
US-12030885-B2 Substituted imidazo[2,1-f][1,2,4]triazines as PI3K-gamma inhibitors PIK3CG, PIK3CD, PIK3R5 NUDT1 3219/4885ADORA2A 2358/4885TLR7 2121/4885
US-20240228498-A1 TERTIARY ALCOHOLS AS PI3K-y INHIBITORS PIK3R5, PIK3R1, PIK3CD NUDT1 4273/4885ADORA2A 4632/4885TLR7 2166/4885
US-12263163-B2 Crystalline succinate salt of 6-(6-aminopyrazin-2-yl)-n-(4-(4-(oxetan-3-yl)piperazin-1-yl)phenyl)imidazo[1,2-a]pyrazin-8-amine as a Syk inhibitor SYK, LCK, LYN NUDT1 4268/4885ADORA2A 4307/4885TLR7 85/4885
US-20030212073-A1 Imidazo[1,2-a]pyrazin-8-ylamines, method of making, and method of use thereof PRKACA, MAP3K8, MAP3K1 NUDT1 820/4885ADORA2A 1231/4885TLR7 3043/4885

“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.