SCHEMBL1604158

SCHEMBL1604158

CC(C)(C)OC(=O)N1C[C@H](F)C[C@H]1CO

nearest known ligand 0.48

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
NR1H2 P55055 1/20 0.48
SRC P12931 8/20 0.41
CHRM2 P08172 1/20 0.37
CHRM1 P11229 1/20 0.37
CHRM3 P20309 1/20 0.37
DPP4 P27487 3/20 0.36
HSD11B1 P28845 1/20 0.36
MEN1 O00255 1/20 0.35
KMT2A Q03164 1/20 0.35

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
SCHEMBL2542677 1.00 NR1H2 (0.48) NR1H2SRCCHRM2CHRM1CHRM3
SCHEMBL29246037 1.00 NR1H2 (0.48) NR1H2SRCCHRM2CHRM1CHRM3
SCHEMBL12183413 1.00 NR1H2 (0.48) NR1H2SRCCHRM2CHRM1CHRM3
SCHEMBL91567 1.00 NR1H2 (0.48) NR1H2SRCCHRM2CHRM1CHRM3
SCHEMBL3855310 1.00 NR1H2 (0.48) NR1H2SRCCHRM2CHRM1CHRM3
SCHEMBL475686 1.00 NR1H2 (0.48) NR1H2SRCCHRM2CHRM1CHRM3
SCHEMBL15270709 1.00 NR1H2 (0.48) NR1H2SRCCHRM2CHRM1CHRM3
SCHEMBL2435233 0.88 NR1H2 (0.42) NR1H2SRCCHRM2CHRM1CHRM3
SCHEMBL23546202 0.86 NR1H2 (0.43) NR1H2SRCCHRM2CHRM1CHRM3
SCHEMBL15057262 0.86 NR1H2 (0.40) NR1H2SRCCHRM2CHRM1CHRM3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12630563-B2 Macrocyclic RIP2-kinase inhibitors ONCODESIGN S.A. (FR) 2026-05-19 US disclosed
US-12630562-B2 Piperidylurea compounds and methods of use thereof ARCUS BIOSCIENCES, INC. (US) 2026-05-19 US disclosed
US-12630566-B2 KRas G12D inhibitors Mirati Therapeutics, Inc. (US) 2026-05-19 US disclosed
US-20260125396-A1 MACROCYCLIC RIP2-KINASE INHIBITORS ONCODESIGN S.A. (FR) 2026-05-07 US disclosed
US-20260042777-A1 PIPERIDYLUREA COMPOUNDS AND METHODS OF USE THEREOF ARCUS BIOSCIENCES, INC. (US) 2026-02-12 US disclosed
EP-4688784-A1 KRAS INHIBITORS Eli Lilly and Company (US) 2026-02-11 EP disclosed
EP-4606377-A2 NOVEL AMINO PYRIMIDINE DERIVATIVES Novartis AG (CH) 2025-08-27 EP disclosed
EP-4219478-B1 METHOD OF PREPARING AMINO PYRIMIDINE DERIVATIVES NOVARTIS AG (CH) 2025-06-11 EP disclosed
EP-3853234-B1 FUSED TRICYCLIC RING DERIVATIVES AS SRC HOMOLOGY-2 PHOSPHATASE INHIBITORS NIKANG THERAPEUTICS INC (US) 2025-04-23 EP disclosed
US-12264167-B2 Fused tricyclic ring derivatives as SRC homology-2 phosphate inhibitors NIKANG THERAPEUTICS, INC. (US) 2025-04-01 US disclosed
US-8269000-B2 Substituted pyrimidine and triazine compounds GRUENENTHAL GMBH (DE) 2012-09-18 US disclosed
WO-2012093101-A1 INDOLE COMPOUNDS OR ANALOGUES THEREOF USEFUL FOR THE TREATMENT OF AGE-RELATED MACULAR DEGENERATION (AMD) NOVARTIS AG (CH) 2012-07-12 WO disclosed
EP-2457903-A1 Cannabinoid receptor ligands Abbott Laboratories (US) 2012-05-30 EP disclosed
EP-2356101-A1 PYRIMIDINE AND TRIAZINE SULFONAMIDE DERIVATES AS B1 BRADYKININ RECEPTOR (B1R) INHIBITORS FOR TREATING PAIN Grünenthal GmbH (DE) 2011-08-17 EP disclosed
EP-2346843-A2 SUBSTITUTED BENZAMIDES AS CANNABINOID RECEPTOR LIGANDS Abbott Laboratories (US) 2011-07-27 EP disclosed
US-20110082165-A1 PYRROLIDINE GPR40 MODULATORS BRISTOL-MYERS SQUIBB COMPANY 2011-04-07 US disclosed
US-20100173889-A1 Substituted Pyrimidine and Triazine Compounds GRUENENTHAL GMBH (DE) 2010-07-08 US disclosed
WO-2010046109-A1 PYRIMIDINE AND TRIAZINE SULFONAMIDE DERIVATES AS B1 BRADYKININ RECEPTOR (B1R) INHIBITORS FOR TREATING PAIN Grünenthal GmbH (DE) 2010-04-29 WO disclosed
US-20100063022-A1 NOVEL COMPOUNDS AS CANNABINOID RECEPTOR LIGANDS ABBOTT LABORATORIES (US) 2010-03-11 US disclosed
WO-2010028338-A2 NOVEL COMPOUNDS AS CANNABINOID RECEPTOR LIGANDS ABBOTT LABORATORIES (US) 2010-03-11 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-12630566-B2 KRas G12D inhibitors KRAS, NRAS, HRAS NR1H2 1715/4885SRC 106/4885CHRM2 4858/4885
US-20100173889-A1 Substituted Pyrimidine and Triazine Compounds ADORA2B, CCNB1, TYMS NR1H2 2976/4885SRC 3337/4885CHRM2 986/4885
US-12630562-B2 Piperidylurea compounds and methods of use thereof CLIC1, HCCS, CNR1 NR1H2 308/4885SRC 1581/4885CHRM2 172/4885
US-20260125396-A1 MACROCYCLIC RIP2-KINASE INHIBITORS RIPK1, RIPK2, RIPK4 NR1H2 167/4885SRC 3102/4885CHRM2 2228/4885
US-12630563-B2 Macrocyclic RIP2-kinase inhibitors RIPK1, RIPK2, RIPK3 NR1H2 804/4885SRC 2369/4885CHRM2 3874/4885
US-12264167-B2 Fused tricyclic ring derivatives as SRC homology-2 phosphate inhibitors SRC, PTPRCAP, PTPRC NR1H2 2154/4885SRC 1/4885CHRM2 4874/4885
US-20110082165-A1 PYRROLIDINE GPR40 MODULATORS GPR55, GPR65, GPR27 NR1H2 160/4885SRC 2794/4885CHRM2 559/4885
US-20260042777-A1 PIPERIDYLUREA COMPOUNDS AND METHODS OF USE THEREOF CBR1, CLIC1, RER1 NR1H2 450/4885SRC 1450/4885CHRM2 185/4885
US-20100063022-A1 NOVEL COMPOUNDS AS CANNABINOID RECEPTOR LIGANDS CNR1, CNR2, NPY1R NR1H2 47/4885SRC 1441/4885CHRM2 52/4885

“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.