SCHEMBL4338135

SCHEMBL4338135

CCOC(=O)c1nnc(O)cc1O

nearest known ligand 0.49

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NR1H2 P55055 1/20 0.49
NR1H3 Q13133 1/20 0.49
CA12 O43570 5/20 0.46
CA1 P00915 5/20 0.46
CA2 P00918 5/20 0.46
CA7 P43166 5/20 0.46
CA9 Q16790 5/20 0.46
CA14 Q9ULX7 5/20 0.46
CYP1A2 P05177 1/20 0.46
CYP2D6 P10635 1/20 0.46
CYP2C19 P33261 1/20 0.46
NPSR1 Q6W5P4 1/20 0.46
SMN1; SMN2 Q16637 2/20 0.45
CYP3A4 P08684 1/20 0.45
TDP1 Q9NUW8 1/20 0.45
NPC1 O15118 3/20 0.43
ALDH1A1 P00352 2/20 0.43
RAB9A P51151 2/20 0.43
KDM4E B2RXH2 1/20 0.42
MAPK1 P28482 1/20 0.42

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
SCHEMBL29739985 1.00 NR1H2 (0.49) NR1H2NR1H3CA12CA1CA2
SCHEMBL23618033 0.84 NR1H2 (0.47) NR1H2NR1H3CA12CA1CA2
SCHEMBL23096154 0.80 CA12 (0.41) NR1H2NR1H3CA12CA1CA2
SCHEMBL4974794 0.79 NPSR1 (0.46) CA12CA1CA2CA7CA9
SCHEMBL30940533 0.79 NPSR1 (0.46) CA12CA1CA2CA7CA9
SCHEMBL18560495 0.73 KDM4E (0.47) NR1H2NR1H3CA12CA1CA2
SCHEMBL17194938 0.72 MEN1 (0.38) SMN1; SMN2CYP3A4ALDH1A1KDM4EMAPK1
SCHEMBL8630212 0.72 CA12 (0.43) NR1H2NR1H3CA12CA1CA2
SCHEMBL29739916 0.71 GLP1R (0.49) CA12CA1CA2CA7CA9
SCHEMBL4019772 0.71 GLP1R (0.49) CA12CA1CA2CA7CA9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12565487-B2 Process for the preparation of 6-(cyclopropaneamido)-4-((2-methoxy-3-(1-methyl-1H-1,2,4-triazol-3-yl)phenyl)amino)-N-(methyl-d3)pyridazine-3-carboxamide BRISTOL-MYERS SQUIBB COMPANY (US) 2026-03-03 US disclosed
US-20260001898-A1 Heteroaryl compounds as inhibitors of TYK2/JAK1, composition and application thereof ACCRO BIOSCIENCE HK LTD (HK) 2026-01-01 US disclosed
US-12492184-B2 Heteroaryl compounds, preparation methods and uses thereof InventisBio Co., Ltd. (CN) 2025-12-09 US disclosed
US-12365667-B2 Sulfone pyridine alkyl amide-substituted heteroaryl compounds BRISTOL-MYERS SQUIBB COMPANY (US) 2025-07-22 US disclosed
EP-4551559-A1 HETEROARYL COMPOUNDS AS INHIBITORS OF TYK2/JAK1, COMPOSITION AND APPLICATION THEREOF Accro Bioscience (HK) Limited (HK) 2025-05-14 EP disclosed
CN-119954772-A Heteroaryl compounds, methods of making and uses thereof 益方生物科技(上海)股份有限公司 2025-05-09 CN disclosed
CN-119954775-A Heteroaryl compounds, methods of making and uses thereof 益方生物科技(上海)股份有限公司 2025-05-09 CN disclosed
US-20240382477-A1 NITROGEN-CONTAINING HETEROCYCLIC PYRIDINE COMPOUND SHANGHAI ZHEYE BIOTECHNOLOGY CO. LTD. (CN) 2024-11-21 US disclosed
US-20240343747-A1 Heteroaryl compounds as inhibitors of TYK2, composition and application thereof ACCRO BIOSCIENCE (HK) LIMITED (HK) 2024-10-17 US disclosed
CN-111315737-B Heteroaryl compounds substituted with sulfone pyridinylalkylamides 百时美施贵宝公司 2024-06-18 CN disclosed
US-9505748-B2 Amide-substituted heterocyclic compounds useful as modulators of IL-12, IL-23 and/or IFNα responses BRISTOL-MYERS SQUIBB COMPANY (US) 2016-11-29 US disclosed
WO-2016120403-A1 ALPHA-D-GALACTOSIDE INHIBITORS OF GALECTINS GALECTO BIOTECH AB (DK) 2016-08-04 WO disclosed
WO-2016120403-A1 ALPHA-D-GALACTOSIDE INHIBITORS OF GALECTINS GALECTO BIOTECH AB (DK) 2016-08-04 WO disclosed
US-20150299183-A1 AMIDE-SUBSTITUTED HETEROCYCLIC COMPOUNDS USEFUL AS MODULATORS OF IL-12, IL-23 AND/OR IFN ALPHA RESPONSES BRISTOL-MYERS SQUIBB COMPANY 2015-10-22 US disclosed
WO-2014074661-A1 AMIDE-SUBSTITUTED HETEROCYCLIC COMPOUNDS USEFUL AS MODULATORS OF IL-12, IL-23 AND/OR IFN ALPHα RESPONSES BRISTOL-MYERS SQUIBB COMPANY (US) 2014-05-15 WO disclosed
US-7576072-B2 Heterocyclic inhibitors of MEK and methods of use thereof ARRAY BIOPHARMA INC. (US) 2009-08-18 US disclosed
EP-1689406-A4 HETEROCYCLIC INHIBITORS OF MEK AND METHODS OF USE THEREOF ARRAY BIOPHARMA INC (US) 2007-01-17 EP disclosed
EP-1689406-A2 HETEROCYCLIC INHIBITORS OF MEK AND METHODS OF USE THEREOF Array Biopharma, Inc. (US) 2006-08-16 EP disclosed
US-20050153942-A1 Heterocyclic inhibitors of MEK and methods of use thereof ARRAY BIOPHARMA INC. 2005-07-14 US disclosed
WO-2005051906-A2 HETEROCYCLIC INHIBITORS OF MEK AND METHODS OF USE THEREOF ARRAY BIOPHARMA INC. (US) 2005-06-09 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 (8 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-20240382477-A1 NITROGEN-CONTAINING HETEROCYCLIC PYRIDINE COMPOUND NNMT, NOD1, NOD2 NR1H2 2780/4885NR1H3 3276/4885CA12 4362/4885
US-20150299183-A1 AMIDE-SUBSTITUTED HETEROCYCLIC COMPOUNDS USEFUL AS MODULATORS OF IL-12, IL-23 AND/OR IFN ALPHA RESPONSES IFNG, IFNAR1, TYK2 NR1H2 1833/4885NR1H3 2123/4885CA12 2379/4885
US-20240343747-A1 Heteroaryl compounds as inhibitors of TYK2, composition and application thereof TYK2, PTK2B, BTK NR1H2 1472/4885NR1H3 1447/4885CA12 4780/4885
US-12565487-B2 Process for the preparation of 6-(cyclopropaneamido)-4-((2-methoxy-3-(1-methyl-1H-1,2,4-triazol-3-yl)phenyl)amino)-N-(methyl-d3)pyridazine-3-carboxamide TYK2, DYRK3, DYRK4 NR1H2 4411/4885NR1H3 4536/4885CA12 2615/4885
US-20260001898-A1 Heteroaryl compounds as inhibitors of TYK2/JAK1, composition and application thereof JAK1, JAK2, TYK2 NR1H2 826/4885NR1H3 800/4885CA12 3342/4885
US-12365667-B2 Sulfone pyridine alkyl amide-substituted heteroaryl compounds TYK2, JAK3, JAK2 NR1H2 2204/4885NR1H3 2264/4885CA12 2843/4885
US-20050153942-A1 Heterocyclic inhibitors of MEK and methods of use thereof NRAS, BRAF, MAPK9 NR1H2 536/4885NR1H3 605/4885CA12 4872/4885
US-12492184-B2 Heteroaryl compounds, preparation methods and uses thereof TYK2, IL2, IL23R NR1H2 888/4885NR1H3 795/4885CA12 3027/4885

“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.