SCHEMBL14977221

SCHEMBL14977221

Fc1cnc2[nH]ncc2c1

nearest known ligand 0.42

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
NAMPT P43490 4/20 0.40
CDC7 O00311 2/20 0.37
PIK3C3 Q8NEB9 3/20 0.36
FGFR1 P11362 1/20 0.36
FGFR2 P21802 1/20 0.36
BRAF P15056 3/20 0.36
SNCA P37840 1/20 0.36
MAPK1 P28482 1/20 0.35
HTT P42858 1/20 0.35
MKNK1 Q9BUB5 1/20 0.35
AKT1 P31749 1/20 0.35
PIK3CA P42336 1/20 0.35
CHEK1 O14757 1/20 0.34
NPC1 O15118 1/20 0.34
RAB9A P51151 1/20 0.34
KDR P35968 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
SCHEMBL12344590 0.74 PIK3C3 (0.37) NAMPTPIK3C3FGFR1BRAFMAPK1
SCHEMBL29930822 0.73 TRPA1 (0.46) CDC7PIK3C3FGFR1BRAFMAPK1
SCHEMBL29705478 0.73 MAPT (0.50) PIK3C3FGFR1BRAFMAPK1HTT
SCHEMBL29705375 0.73 FGFR1 (0.40) NAMPTPIK3C3FGFR1FGFR2BRAF
SCHEMBL15243458 0.73 NOS1 (0.50) PIK3C3FGFR1BRAFMAPK1HTT
SCHEMBL3429629 0.73 PIK3C3 (0.36) PIK3C3FGFR1BRAFMAPK1HTT
SCHEMBL1496196 0.73 MAPT (0.50) PIK3C3FGFR1BRAFMAPK1HTT
SCHEMBL10329 0.73 DYRK1A (0.50) PIK3C3FGFR1MAPK1HTTMKNK1
SCHEMBL20674185 0.73 FGFR1 (0.40) NAMPTPIK3C3FGFR1FGFR2BRAF
SCHEMBL11982852 0.73 PIK3C3 (0.36) NAMPTPIK3C3FGFR1BRAFMAPK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113354638-A Preparation method of 5-fluoro-3-iodo-1H-pyrazolo [3,4-b ] pyridine 天津敬康生物科技有限公司 2021-09-07 CN claimed
US-20260108546-A1 GIP RECEPTOR AGONIST COMPOUNDS LILLY CO ELI (US) 2026-04-23 US disclosed
US-20260091048-A1 GIP RECEPTOR AGONIST COMPOUNDS LILLY CO ELI (US) 2026-04-02 US disclosed
US-12577243-B2 Monoacylglycerol lipase modulators JANSSEN PHARMACEUTICA NV (BE) 2026-03-17 US disclosed
WO-2025264700-A1 GIP RECEPTOR AGONIST COMPOUNDS ELI LILLY AND COMPANY (US) 2025-12-26 WO disclosed
US-20250197399-A1 COMPOUNDS, COMPOSITIONS, AND METHODS TENVIE THERAPEUTICS, INC. 2025-06-19 US disclosed
US-12275720-B2 Small molecule inhibitors of galectin-3 BRISTOL-MYERS SQUIBB COMPANY (US) 2025-04-15 US disclosed
WO-2025052129-A1 PYRIDINE DERIVATIVES WHICH ACT AS INHIBITORS OF MPTP. NRG THERAPEUTICS LTD (GB) 2025-03-13 WO disclosed
EP-4499626-A1 COMPOUNDS, COMPOSITIONS, AND METHODS Nico Therapeutics, Inc. (US) 2025-02-05 EP disclosed
CN-119233972-A Compounds, compositions, and methods 尼科治疗有限公司 2024-12-31 CN disclosed
EP-2896617-B1 METHOD FOR PRODUCING SUBSTITUTED (Z)-ALPHA-FLUORO-BETA-AMINO-ACRYLALDEHYDES ADVERIO PHARMA GMBH (DE) 2016-10-05 EP disclosed
US-20160009671-A1 PROCESS FOR PREPARING SUBSTITUTED 5-FLUORO-1H-PYRAZOLOPYRIDINES ADVERIO PHARMA GMBH (DE) 2016-01-14 US disclosed
US-9150573-B2 Process for preparing substituted 5-fluoro-1H-pyrazolopyridines ADVERIO PHARMA GMBH (DE) 2015-10-06 US disclosed
EP-2896617-A1 Method for producing substituted 5-fluoro-1h-pyrazolopyridines Adverio Pharma GmbH (DE) 2015-07-22 EP disclosed
US-20140315926-A1 Process for preparing substituted 5-fluoro-1H-pyrazolopyridines ADVERIO PHARMA GMBH (DE) 2014-10-23 US disclosed
EP-2782914-A1 METHOD FOR PRODUCING SUBSTITUTED 5-FLUORO-1H-PYRAZOLOPYRIDINES Bayer Pharma Aktiengesellschaft (DE) 2014-10-01 EP disclosed
US-8802847-B2 Process for preparing substituted 5-fluoro-1H-pyrazolopyridines BAYER INTELLECTUAL PROPERTY GMBH (DE) 2014-08-12 US disclosed
US-20130211090-A1 METHOD FOR THE PRODUCTION OF 5-FLUORO-1H-PYRAZOLO[3,4-B]PYRIDINE-3-CARBONITRILE BAYER INTELLECTUAL PROPERTY GMBH (DE) 2013-08-15 US disclosed
US-20130143900-A1 Process for preparing substituted 5-fluoro-1H-pyrazolopyridines BAYER INTELLECTUAL PROPERTY GMBH (DE) 2013-06-06 US disclosed
WO-2013076168-A1 METHOD FOR PRODUCING SUBSTITUTED 5-FLUORO-1H-PYRAZOLOPYRIDINES BAYER PHARMA AKTIENGESELLSCHAFT (DE) 2013-05-30 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 (9 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-12275720-B2 Small molecule inhibitors of galectin-3 LGALS3, LGALS3BP, LGALS1 NAMPT 849/4885CDC7 3503/4885PIK3C3 2017/4885
US-20130211090-A1 METHOD FOR THE PRODUCTION OF 5-FLUORO-1H-PYRAZOLO[3,4-B]PYRIDINE-3-CARBONITRILE CYP4F3, CYP2F1, CYP4B1 NAMPT 273/4885CDC7 2921/4885PIK3C3 2958/4885
US-12577243-B2 Monoacylglycerol lipase modulators MGLL, LPL, FAAH NAMPT 4738/4885CDC7 3905/4885PIK3C3 3285/4885
US-20160009671-A1 PROCESS FOR PREPARING SUBSTITUTED 5-FLUORO-1H-PYRAZOLOPYRIDINES CYP3A5, CYP4F2, CYP2F1 NAMPT 1428/4885CDC7 3085/4885PIK3C3 2625/4885
US-20260091048-A1 GIP RECEPTOR AGONIST COMPOUNDS GIPR, GLP1R, GPR119 NAMPT 4430/4885CDC7 3436/4885PIK3C3 3694/4885
US-20260108546-A1 GIP RECEPTOR AGONIST COMPOUNDS GIPR, GLP1R, GCGR NAMPT 4439/4885CDC7 3110/4885PIK3C3 3524/4885
US-20130143900-A1 Process for preparing substituted 5-fluoro-1H-pyrazolopyridines CYP3A5, CYP4F2, CYP2F1 NAMPT 1428/4885CDC7 3085/4885PIK3C3 2625/4885
US-20140315926-A1 Process for preparing substituted 5-fluoro-1H-pyrazolopyridines CYP3A5, CYP4F2, CYP2F1 NAMPT 1428/4885CDC7 3085/4885PIK3C3 2625/4885
US-20250197399-A1 COMPOUNDS, COMPOSITIONS, AND METHODS NLRP3, NLRP1, NOD1 NAMPT 294/4885CDC7 2150/4885PIK3C3 1577/4885

“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.