SCHEMBL91557

SCHEMBL91557

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

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PEPD P12955 1/20 0.48
XPNPEP1 Q9NQW7 1/20 0.48
PTPN1 P18031 1/20 0.43
MMP2 P08253 2/20 0.42
ANPEP P15144 2/20 0.42
NR1H2 P55055 2/20 0.41
NR1H3 Q13133 1/20 0.41
CYP1A2 P05177 1/20 0.39
POLB P06746 1/20 0.39
CYP3A4 P08684 1/20 0.39
CYP2C19 P33261 1/20 0.39
DPP4 P27487 6/20 0.37
DPP8 Q6V1X1 1/20 0.37
DPP7 Q9UHL4 1/20 0.37
CHRM2 P08172 1/20 0.36
CHRM1 P11229 1/20 0.36
CHRM3 P20309 1/20 0.36
ALDH1A1 P00352 1/20 0.36
HSD11B1 P28845 1/20 0.36
P2RX3 P56373 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
SCHEMBL476146 1.00 PEPD (0.48) PEPDXPNPEP1PTPN1MMP2ANPEP
SCHEMBL4250662 1.00 PEPD (0.48) PEPDXPNPEP1PTPN1MMP2ANPEP
SCHEMBL3643891 1.00 PEPD (0.48) PEPDXPNPEP1PTPN1MMP2ANPEP
SCHEMBL3552873 1.00 PEPD (0.48) PEPDXPNPEP1PTPN1MMP2ANPEP
SCHEMBL2995724 1.00 PEPD (0.48) PEPDXPNPEP1PTPN1MMP2ANPEP
SCHEMBL3554330 1.00 PEPD (0.48) PEPDXPNPEP1PTPN1MMP2ANPEP
SCHEMBL18591298 1.00 PEPD (0.48) PEPDXPNPEP1PTPN1MMP2ANPEP
SCHEMBL19219868 1.00 PEPD (0.48) PEPDXPNPEP1PTPN1MMP2ANPEP
SCHEMBL29827776 0.91 NR1H2 (0.39) PEPDXPNPEP1PTPN1NR1H2NR1H3
SCHEMBL29947782 0.91 NR1H2 (0.39) PEPDXPNPEP1PTPN1NR1H2NR1H3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260109714-A1 PYRIMIDINE-FUSED RING COMPOUND, AND PREPARATION METHOD THEREFOR AND USE THEREOF GENFLEET THERAPEUTICS SHANGHAI INC (CN) 2026-04-23 US disclosed
US-20260062425-A1 AZA-TETRACYCLIC OXAZEPINE COMPOUNDS AND USES THEREOF GENENTECH INC (US) 2026-03-05 US disclosed
US-20250326766-A1 RIPK1 INHIBITORS AND METHODS OF USE MERCK SHARP & DOHME LLC (US) 2025-10-23 US disclosed
EP-4592295-A1 PYRIMIDINE-FUSED RING COMPOUND, AND PREPARATION METHOD THEREFOR AND USE THEREOF Genfleet Therapeutics (Shanghai) Inc. (CN) 2025-07-30 EP disclosed
US-12338256-B2 Aza-tetracyclic oxazepine compounds and uses thereof GENENTECH, INC. (US) 2025-06-24 US disclosed
WO-2025106362-A1 RIPK1 INHIBITORS AND METHODS OF USE MERCK SHARP & DOHME LLC (US) 2025-05-22 WO disclosed
EP-4526300-A1 RIPK1 INHIBITORS AND METHODS OF USE Merck Sharp & Dohme LLC (US) 2025-03-26 EP disclosed
EP-4526309-A1 AZA-TETRACYCLIC OXAZEPINE COMPOUNDS AND USES THEREOF Genentech, Inc. (US) 2025-03-26 EP disclosed
WO-2025026903-A1 IMIDAZO PYRIMIDINE COMPOUNDS FOR THE TREATMENT OF CANCER BAYER AKTIENGESELLSCHAFT (DE) 2025-02-06 WO disclosed
EP-4305038-B1 KRAS G12D INHIBITORS BRISTOL MYERS SQUIBB CO (US) 2025-01-29 EP disclosed
US-20080125589-A1 Process for Production of Fluoro Derivative CENTRAL GLASS COMPANY, LIMITED (JP) 2008-05-29 US disclosed
US-20080114053-A1 Method for Producing Fluorinated Proline Derivative MITSUI CHEMICALS, INC. (JP) 2008-05-15 US disclosed
US-20080114053-A1 Method for Producing Fluorinated Proline Derivative MITSUI CHEMICALS, INC. (JP) 2008-05-15 US disclosed
US-7279584-B2 Method for production of cis-4-fluoro-L-proline derivatives TAISHO PHARMACEUTICAL CO., LTD. (JP) 2007-10-09 US disclosed
US-7279584-B2 Method for production of cis-4-fluoro-L-proline derivatives TAISHO PHARMACEUTICAL CO., LTD. (JP) 2007-10-09 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
US-20070232601-A1 Vla-4 Inhibitor DAIICHI PHARMACEUTICAL CO., LTD. (JP) 2007-10-04 US disclosed
EP-1757602-A1 VLA-4 INHIBITOR DAIICHI PHARMACEUTICAL CO., LTD. (JP) 2007-02-28 EP disclosed
US-20060281927-A1 Process for production of cis-4-fluoro-l-proline derivatives TAISHO PHARMACEUTICAL CO., LTD. (JP) 2006-12-14 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 (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-20080125589-A1 Process for Production of Fluoro Derivative PFAS, PFKFB2, PFKFB1 PEPD 3407/4885XPNPEP1 4402/4885PTPN1 4355/4885
US-12338256-B2 Aza-tetracyclic oxazepine compounds and uses thereof AZI2, TET3, OXA1L PEPD 2977/4885XPNPEP1 2128/4885PTPN1 2229/4885
US-20070232601-A1 Vla-4 Inhibitor VCAM1, ITGB4, ITGA4 PEPD 4331/4885XPNPEP1 3603/4885PTPN1 988/4885
US-20260109714-A1 PYRIMIDINE-FUSED RING COMPOUND, AND PREPARATION METHOD THEREFOR AND USE THEREOF KRAS, NRAS, HRAS PEPD 4815/4885XPNPEP1 3047/4885PTPN1 987/4885
US-20080114053-A1 Method for Producing Fluorinated Proline Derivative LPO, NPFFR1, NPFFR2 PEPD 2007/4885XPNPEP1 1214/4885PTPN1 2372/4885
US-20260062425-A1 AZA-TETRACYCLIC OXAZEPINE COMPOUNDS AND USES THEREOF KRAS, NRAS, HRAS PEPD 4765/4885XPNPEP1 4293/4885PTPN1 975/4885
US-20060281927-A1 Process for production of cis-4-fluoro-l-proline derivatives PRAP1, P4HA1, SLC6A7 PEPD 10/4885XPNPEP1 187/4885PTPN1 2933/4885
US-20250326766-A1 RIPK1 INHIBITORS AND METHODS OF USE RIPK1, RIPK2, RIPK3 PEPD 3930/4885XPNPEP1 1850/4885PTPN1 1725/4885

“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.