SCHEMBL1835481

SCHEMBL1835481

Nc1ccnc2[nH]ncc12

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
XDH P47989 2/20 0.53
RET P07949 1/20 0.53
PI4KA P42356 1/20 0.53
LRRK2 Q5S007 1/20 0.53
PI4K2B Q8TCG2 1/20 0.53
PI4K2A Q9BTU6 1/20 0.53
PI4KB Q9UBF8 1/20 0.53
PDPK1 O15530 1/20 0.48
PIK3CD O00329 1/20 0.46
PIK3CA P42336 1/20 0.46
PIK3CB P42338 1/20 0.46
NUDT1 P36639 1/20 0.45
AURKA O14965 2/20 0.43
BRD4 O60885 1/20 0.43
CHEK1 O14757 1/20 0.43
MAPK1 P28482 2/20 0.42
LMNA P02545 3/20 0.41
TSHR P16473 1/20 0.41
ADORA2A P29274 1/20 0.41
SLC6A4 P31645 1/20 0.41

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
SCHEMBL29487195 1.00 XDH (0.53) XDHRETPI4KALRRK2PI4K2B
Hydrochloric Acid SCHEMBL2247697 0.98 XDH (0.52) XDHRETPI4KALRRK2PI4K2B
Hydrochloric Acid SCHEMBL2596063 0.98 XDH (0.52) XDHRETPI4KALRRK2PI4K2B
SCHEMBL3934403 0.81 TSHR (0.43) XDHRETPI4KALRRK2PI4K2B
SCHEMBL11618063 0.76 PDPK1 (0.46) XDHRETPI4KALRRK2PI4K2B
SCHEMBL3375875 0.75 PRKCI (0.52) XDHRETPI4KALRRK2PI4K2B
SCHEMBL9933985 0.75 NUDT1 (0.49) XDHRETPI4KALRRK2PI4K2B
SCHEMBL11506 0.75 NUDT1 (0.53) XDHRETPI4KALRRK2PI4K2B
SCHEMBL21855766 0.75 PIK3CD (0.46) XDHRETPI4KALRRK2PI4K2B
SCHEMBL2112472 0.75 PIK3CD (0.46) XDHRETPI4KALRRK2PI4K2B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118146219-A Preparation process of 1H-pyrazolo [3,4-b ] pyridine-4-amine intermediate 南京艾康生物科技有限公司 2024-06-07 CN claimed
WO-2025215582-A1 SUBSTITUTED PYRAZOLOPYRIDINE AND PYRAZOLOPYRIMIDINE COMPOUNDS AND THEIR USE GT GAIN THERAPEUTICS SA (CH) 2025-10-16 WO disclosed
CN-118146219-A Preparation process of 1H-pyrazolo [3,4-b ] pyridine-4-amine intermediate 南京艾康生物科技有限公司 2024-06-07 CN disclosed
CN-118146219-A Preparation process of 1H-pyrazolo [3,4-b ] pyridine-4-amine intermediate 南京艾康生物科技有限公司 2024-06-07 CN disclosed
CN-118146219-A Preparation process of 1H-pyrazolo [3,4-b ] pyridine-4-amine intermediate 南京艾康生物科技有限公司 2024-06-07 CN disclosed
WO-2023220402-A1 ENPP1 MODULATORS AND PRODUCTS AND USES THEREOF GOSSAMER BIO SERVICES, INC. (US) 2023-11-16 WO disclosed
WO-2020065613-A1 MONOACYLGLYCEROL LIPASE MODULATORS JANSSEN PHARMACEUTICA NV (BE) 2020-04-02 WO disclosed
EP-3558988-A1 PYRAZOLO[3,4-B]PYRIDINES AND IMIDAZO[1,5-B]PYRIDAZINES AS PDE1 INHIBITORS H. Lundbeck A/S (DK) 2019-10-30 EP disclosed
WO-2018115067-A1 PYRAZOLO[3,4-B]PYRIDINES AND IMIDAZO[1,5-B]PYRIDAZINES AS PDE1 INHIBITORS H. LUNDBECK A/S (DK) 2018-06-28 WO disclosed
US-20170145009-A1 HETEROCYCLIC COMPOUNDS THAT INHIBIT THE KINASE ACTIVITY OF MNK USEFUL FOR TREATING VARIOUS CANCERS EFFECTOR THERAPEUTICS, INC. 2017-05-25 US disclosed
WO-2007036734-A1 PYRAZOLO[3,4-B]PYRIDINE COMPOUND, AND ITS USE AS A PDE4 INHIBITOR GLAXO GROUP LIMITED (GB) 2007-04-05 WO disclosed
WO-2007036733-A1 PYRAZOLO[3,4-B]PYRIDINE COMPOUNDS, AND THEIR USE AS PDE4 INHIBITORS GLAXO GROUP LIMITED (GB) 2007-04-05 WO disclosed
WO-2006047516-A2 COMPOUNDS AND COMPOSITIONS AS INHIBITORS OF CANNABINOID RECEPTOR 1 ACTIVITY IRM LLC (BM) 2006-05-04 WO disclosed
EP-1581532-A1 PYRAZOLO[3,4-B]PYRIDINE COMPOUNDS, AND THEIR USE AS PHOSPHODIESTERASE INHIBITORS GLAXO GROUP LIMITED (GB) 2005-10-05 EP disclosed
WO-2004056823-A1 PYRAZOLO[3,4-b]PYRIDINE COMPOUNDS, AND THEIR USE AS PHOSPHODIESTERASE INHIBITORS GLAXO GROUP LIMITED (GB) 2004-07-08 WO disclosed
EP-1391454-A1 Substituted benzamide compounds with antihypertensive activity Mitsubishi Pharma Corporation (JP) 2004-02-25 EP disclosed
EP-1195372-A1 N-heterocyclic substituted benzamide derivatives with antihypertensive activity Mitsubishi Pharma Corporation (JP) 2002-04-10 EP disclosed
US-6156766-A Benzamide compounds and pharmaceutical use thereof YOSHITOMI PHARMACEUTICAL INDUSTRIES, LTD. (JP) 2000-12-05 US disclosed
US-5958944-A TREATMENT OF CIRCULATORY DISEASES IN CORONARY, CEREBRAL, RENAL AND PERIPHERAL ARTERIES, AS A THERAPEUTIC AGENT FOR HYPERTENSION, ANGINA PECTORIS, AND RENAL AND PERIPHERAL CIRCULATION DISORDER, ANTIASTHMATIC AGENT YOSHITOMI PHARMACEUTICAL INDUSTRIES, LTD. (JP) 1999-09-28 US disclosed
EP-0757038-A1 BENZAMIDE COMPOUND AND MEDICINAL USE THEREOF YOSHITOMI PHARMACEUTICAL INDUSTRIES, LTD. (JP) 1997-02-05 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 (1 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-20170145009-A1 HETEROCYCLIC COMPOUNDS THAT INHIBIT THE KINASE ACTIVITY OF MNK USEFUL FOR TREATING VARIOUS CANCERS MAP3K9, MAP3K19, MAP3K20 XDH 3031/4885RET 307/4885PI4KA 382/4885

“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.