SCHEMBL6857673

SCHEMBL6857673

COC(=O)[C@@H]1C[C@@H](OC)CN1C(=O)OC(C)(C)C

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
UCHL1 P09936 1/20 0.46
MMP2 P08253 2/20 0.42
ANPEP P15144 2/20 0.42
P2RX3 P56373 1/20 0.41
NR1H2 P55055 2/20 0.41
NR1H3 Q13133 1/20 0.41
PTPN1 P18031 1/20 0.40
CYP1A2 P05177 1/20 0.39
POLB P06746 1/20 0.39
CYP3A4 P08684 1/20 0.39
CYP2C19 P33261 1/20 0.39
CHRM2 P08172 1/20 0.36
CHRM1 P11229 1/20 0.36
CHRM3 P20309 1/20 0.36
ALDH1A1 P00352 1/20 0.36
PDE4B Q07343 1/20 0.35
HTRA1 Q92743 1/20 0.35
HSD17B10 Q99714 1/20 0.35
MCL1 Q07820 1/20 0.34
CCR2 P41597 1/20 0.33

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
SCHEMBL8269126 1.00 UCHL1 (0.46) UCHL1MMP2ANPEPP2RX3NR1H2
SCHEMBL3833792 1.00 UCHL1 (0.46) UCHL1MMP2ANPEPP2RX3NR1H2
SCHEMBL7921977 1.00 UCHL1 (0.46) UCHL1MMP2ANPEPP2RX3NR1H2
SCHEMBL92870 1.00 UCHL1 (0.46) UCHL1MMP2ANPEPP2RX3NR1H2
SCHEMBL10215471 1.00 UCHL1 (0.46) UCHL1MMP2ANPEPP2RX3NR1H2
SCHEMBL19388625 1.00 UCHL1 (0.46) UCHL1MMP2ANPEPP2RX3NR1H2
SCHEMBL13163958 1.00 UCHL1 (0.46) UCHL1MMP2ANPEPP2RX3NR1H2
SCHEMBL31107813 0.92 UCHL1 (0.47) UCHL1MMP2ANPEPP2RX3NR1H2
SCHEMBL24739170 0.90 MMP2 (0.41) UCHL1MMP2ANPEPP2RX3NR1H2
SCHEMBL18586768 0.90 MMP2 (0.41) UCHL1MMP2ANPEPP2RX3NR1H2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12630566-B2 KRas G12D inhibitors Mirati Therapeutics, Inc. (US) 2026-05-19 US disclosed
EP-4688784-A1 KRAS INHIBITORS Eli Lilly and Company (US) 2026-02-11 EP disclosed
US-20250346585-A1 PHARMACEUTICAL COMPOUNDS FOR THE TREATMENT OF COMPLEMENT MEDIATED DISORDERS ALEXION PHARMACEUTICALS, INC. (US) 2025-11-13 US disclosed
US-12286429-B2 5-oxo-1,2,3,5,8,8a-hexahydroindolizine-3-carboxamide derivatives useful as a factor XIa inhibitors JANSSEN PHARMACEUTICA NV (BE) 2025-04-29 US disclosed
US-20250101043-A1 KRAS INHIBITORS ELI LILLY AND COMPANY 2025-03-27 US disclosed
US-20250059163-A1 FUSED RING COMPOUNDS GENENTECH INC (US) 2025-02-20 US disclosed
EP-4483881-A2 FUSED RING COMPOUNDS F. Hoffmann-La Roche AG (CH) 2025-01-01 EP disclosed
CN-113004269-B Heterocyclic compounds of Kras-G12C inhibitors 首药控股(北京)股份有限公司 2024-11-05 CN disclosed
US-20240343736-A1 KRAS INHIBITORS ELI LILLY AND COMPANY 2024-10-17 US disclosed
WO-2024206747-A1 KRAS INHIBITORS ELI LILLY AND COMPANY (US) 2024-10-03 WO disclosed
US-20130273005-A1 METHODS FOR TREATING HCV GILEAD SCIENCES, INC. (US) 2013-10-17 US disclosed
US-20130273005-A1 METHODS FOR TREATING HCV GILEAD SCIENCES, INC. (US) 2013-10-17 US disclosed
US-20130243726-A1 METHODS FOR TREATING HCV GILEAD PHARMASSET LLC (US) 2013-09-19 US disclosed
US-20130243726-A1 METHODS FOR TREATING HCV GILEAD PHARMASSET LLC (US) 2013-09-19 US disclosed
US-20130165462-A1 HETEROARYL COMPOUNDS AND USES THEREOF CELGENE AVILOMICS RESEARCH, INC. (US) 2013-06-27 US disclosed
US-8389560-B2 HCV protease inhibitors TAIGEN BIOTECHNOLOGY CO., LTD. (TW) 2013-03-05 US disclosed
US-20110065737-A1 HCV PROTEASE INHIBITORS TAIGEN BIOTECHNOLOGY CO., LTD. (TW) 2011-03-17 US disclosed
US-20090286814-A1 HCV PROTEASE INHIBITORS TAIGEN BIOTECHNOLOGY CO., LTD. (TW) 2009-11-19 US disclosed
US-20070232601-A1 Vla-4 Inhibitor DAIICHI PHARMACEUTICAL CO., LTD. (JP) 2007-10-04 US disclosed
US-20070232601-A1 Vla-4 Inhibitor DAIICHI PHARMACEUTICAL CO., LTD. (JP) 2007-10-04 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 (12 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-20240343736-A1 KRAS INHIBITORS KRAS, NRAS, HRAS UCHL1 4229/4885MMP2 3751/4885ANPEP 4125/4885
US-12286429-B2 5-oxo-1,2,3,5,8,8a-hexahydroindolizine-3-carboxamide derivatives useful as a factor XIa inhibitors F11, F12, F13A1 UCHL1 2717/4885MMP2 230/4885ANPEP 783/4885
US-20130243726-A1 METHODS FOR TREATING HCV HAVCR2, DHFR, HCCS UCHL1 3263/4885MMP2 2284/4885ANPEP 981/4885
US-20070232601-A1 Vla-4 Inhibitor VCAM1, ITGB4, ITGA4 UCHL1 4517/4885MMP2 975/4885ANPEP 1916/4885
US-12630566-B2 KRas G12D inhibitors KRAS, NRAS, HRAS UCHL1 3052/4885MMP2 1803/4885ANPEP 4438/4885
US-20250059163-A1 FUSED RING COMPOUNDS KRAS, NRAS, HRAS UCHL1 3731/4885MMP2 3256/4885ANPEP 4044/4885
US-20110065737-A1 HCV PROTEASE INHIBITORS RNASE1, HAVCR2, CTRL UCHL1 195/4885MMP2 168/4885ANPEP 16/4885
US-20250346585-A1 PHARMACEUTICAL COMPOUNDS FOR THE TREATMENT OF COMPLEMENT MEDIATED DISORDERS C5, C1S, C9 UCHL1 3984/4885MMP2 3537/4885ANPEP 1871/4885
US-20090286814-A1 HCV PROTEASE INHIBITORS HAVCR2, SPINT2, RNASE1 UCHL1 200/4885MMP2 159/4885ANPEP 19/4885
US-20130273005-A1 METHODS FOR TREATING HCV HAVCR2, HCCS, LIPC UCHL1 2586/4885MMP2 1083/4885ANPEP 808/4885
US-20130165462-A1 HETEROARYL COMPOUNDS AND USES THEREOF ABCG2, CYP3A43, CYP3A5 UCHL1 1518/4885MMP2 2607/4885ANPEP 1161/4885
US-20250101043-A1 KRAS INHIBITORS KRAS, NRAS, HRAS UCHL1 4229/4885MMP2 3751/4885ANPEP 4125/4885

“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.