SCHEMBL4526748

SCHEMBL4526748

Cn1ncc2c(F)c(Br)ccc21

nearest known ligand 0.58

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HTT P42858 1/20 0.34
SMN1; SMN2 Q16637 1/20 0.34
CCR4 P51679 2/20 0.33
HTR1A P08908 1/20 0.33
HTR7 P34969 1/20 0.33
HTR6 P50406 1/20 0.33
GAA P10253 1/20 0.32
APP P05067 1/20 0.31
MAPT P10636 2/20 0.31
KDM4E B2RXH2 1/20 0.31
MEN1 O00255 1/20 0.31
ALDH1A1 P00352 1/20 0.31
MAPK1 P28482 1/20 0.31
KMT2A Q03164 1/20 0.31
NPSR1 Q6W5P4 1/20 0.31
TRPA1 O75762 1/20 0.31
MAOB P27338 1/20 0.31
HTR2C P28335 2/20 0.31
CDK2 P24941 1/20 0.30
FLT3 P36888 1/20 0.30

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
SCHEMBL31472061 0.88
SCHEMBL15518859 0.79 BRD4 (0.36) HTTSMN1; SMN2CCR4MAPTKDM4E
SCHEMBL13676392 0.79 PIP4K2A (0.38) CCR4APPTRPA1MAOBCDK2
SCHEMBL29769114 0.79 PIP4K2A (0.38) CCR4APPTRPA1MAOBCDK2
SCHEMBL23115842 0.78 MAOB (0.36) HTTSMN1; SMN2GAAAPPMAPT
SCHEMBL20015374 0.78 CCR4 (0.39) CCR4MAPTKDM4EMEN1ALDH1A1
SCHEMBL31424338 0.78 PI4KA (0.37) CCR4APPMAPTALDH1A1TRPA1
SCHEMBL31500712 0.78 PI4KA (0.37) CCR4MAPTKDM4EMEN1ALDH1A1
SCHEMBL16738868 0.78 IDO1 (0.32) CCR4GAAMAPTKDM4EMEN1
SCHEMBL31500705 0.78 ALDH1A1 (0.32) CCR4MAPTKDM4EMEN1ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260138998-A1 GLP-1 RECEPTOR AGONISTS AND METHODS OF USE MERCK SHARP & DOHME LLC (US) 2026-05-21 US disclosed
WO-2025124357-A9 HETEROCYCLIC GLP-1 RECEPTOR AGONIST AND USE THEREOF 广东众生睿创生物科技有限公司 2026-05-15 WO disclosed
CN-122010981-A GLP-1 receptor agonism/GLP-1 secretagogue double-target compound 仁奎医药科技(北京)有限公司 2026-05-12 CN disclosed
US-12617783-B2 Heterocyclic GLP-1R agonists BIOMEA FUSION, INC. (US) 2026-05-05 US disclosed
WO-2026087442-A1 AMINO-IMIDAZOLE ANTIBACTERIAL COMPOUNDS F. HOFFMANN-LA ROCHE AG (CH) 2026-04-30 WO disclosed
US-20260103463-A1 PYRAZOLOPYRIDINE DERIVATIVE HAVING GLP-1 RECEPTOR AGONIST EFFECT CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2026-04-16 US disclosed
CN-121850947-A Preparation method of GLP-1 agonist intermediate and compound 成都博腾药业有限公司 2026-04-14 CN disclosed
US-12595264-B2 Heterocyclic GLP-1 agonists GASHERBRUM BIO, INC. (US) 2026-04-07 US disclosed
US-20260055105-A1 PYRAZOLOPYRIDINE DERIVATIVE HAVING GLP-1 RECEPTOR AGONIST EFFECT CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2026-02-26 US disclosed
US-20250339411-A1 GLP-1R AGONIST COMPOUND AND USE THEREOF CHONGQING PHARMACEUTICAL RES INSTITUTE CO LTD (CN) 2025-11-06 US disclosed
CN-110740991-A Novel biphenyl compound or salt thereof 大鹏药品工业株式会社 2020-01-31 CN disclosed
EP-3517538-A1 PYRAZOLOPYRIDINE DERIVATIVE HAVING GLP-1 RECEPTOR AGONIST EFFECT Chugai Seiyaku Kabushiki Kaisha (JP) 2019-07-31 EP disclosed
EP-3517538-A1 PYRAZOLOPYRIDINE DERIVATIVE HAVING GLP-1 RECEPTOR AGONIST EFFECT Chugai Seiyaku Kabushiki Kaisha (JP) 2019-07-31 EP disclosed
US-20190225604-A1 PYRAZOLOPYRIDINE DERIVATIVE HAVING GLP-1 RECEPTOR AGONIST EFFECT CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2019-07-25 US disclosed
US-20190225604-A1 PYRAZOLOPYRIDINE DERIVATIVE HAVING GLP-1 RECEPTOR AGONIST EFFECT CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2019-07-25 US disclosed
US-20180354960-A1 NOVEL BIPHENYL COMPOUND OR SALT THEREOF TAIHO PHARMACEUTICAL CO., LTD. (JP) 2018-12-13 US disclosed
EP-3381896-A1 NOVEL BIPHENYL COMPOUND OR SALT THEREOF Taiho Pharmaceutical Co., Ltd. (JP) 2018-10-03 EP disclosed
WO-2018056453-A1 PYRAZOLOPYRIDINE DERIVATIVE HAVING GLP-1 RECEPTOR AGONIST EFFECT 中外製薬株式会社 2018-03-29 WO disclosed
US-8822468-B2 3-Methyl-imidazo[1,2-b]pyridazine derivatives NOVARTIS AG (CH) 2014-09-02 US disclosed
US-20090264406-A1 3-METHYL-IMIDAZO[1,2-B]PYRIDAZINE DERIVATIVES NOVARTIS AG 2009-10-22 US 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-20190225604-A1 PYRAZOLOPYRIDINE DERIVATIVE HAVING GLP-1 RECEPTOR AGONIST EFFECT GLP1R, GPR119, GIPR HTT 2783/4885SMN1; SMN2 3453/4885CCR4 4075/4885
US-20090264406-A1 3-METHYL-IMIDAZO[1,2-B]PYRIDAZINE DERIVATIVES MET, ERBB2, ALK HTT 3764/4885SMN1; SMN2 765/4885CCR4 2400/4885
US-12617783-B2 Heterocyclic GLP-1R agonists GLP1R, GIPR, GPR119 HTT 2184/4885SMN1; SMN2 3598/4885CCR4 1573/4885
US-20260138998-A1 GLP-1 RECEPTOR AGONISTS AND METHODS OF USE GLP1R, GIPR, GPR119 HTT 1647/4885SMN1; SMN2 3547/4885CCR4 303/4885
US-12595264-B2 Heterocyclic GLP-1 agonists GLP1R, GIPR, GCGR HTT 2254/4885SMN1; SMN2 2362/4885CCR4 665/4885
US-20180354960-A1 NOVEL BIPHENYL COMPOUND OR SALT THEREOF KDM1B, HDAC1, DOT1L HTT 3125/4885SMN1; SMN2 2791/4885CCR4 4056/4885
US-20260103463-A1 PYRAZOLOPYRIDINE DERIVATIVE HAVING GLP-1 RECEPTOR AGONIST EFFECT GLP1R, GPR119, GIPR HTT 3268/4885SMN1; SMN2 2889/4885CCR4 1136/4885
US-20250339411-A1 GLP-1R AGONIST COMPOUND AND USE THEREOF GLP1R, GIPR, GPR119 HTT 1595/4885SMN1; SMN2 2057/4885CCR4 3950/4885
US-20260055105-A1 PYRAZOLOPYRIDINE DERIVATIVE HAVING GLP-1 RECEPTOR AGONIST EFFECT GLP1R, GIPR, GPR119 HTT 3315/4885SMN1; SMN2 2230/4885CCR4 2701/4885

“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.