SCHEMBL3771173

SCHEMBL3771173

CCO[C@H]1CN[C@H](C(=O)O)C1

nearest known ligand 0.47

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
CYP2D6 P10635 3/20 0.47
CYP1A2 P05177 2/20 0.47
ALOX15 P16050 2/20 0.47
CYP2C19 P33261 2/20 0.47
SLC1A3 P43003 1/20 0.47
SLC1A2 P43004 1/20 0.47
SLC1A1 P43005 1/20 0.47
ARG1 P05089 1/20 0.41
LMNA P02545 2/20 0.37
BLM P54132 2/20 0.37
TSHR P16473 1/20 0.37
RAB9A P51151 1/20 0.37
MEN1 O00255 1/20 0.37
THRB P10828 1/20 0.37
PMP22 Q01453 1/20 0.37
KMT2A Q03164 1/20 0.37

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
SCHEMBL7340980 1.00 CYP2D6 (0.47) CYP2D6CYP1A2ALOX15CYP2C19SLC1A3
SCHEMBL3450012 1.00 CYP2D6 (0.47) CYP2D6CYP1A2ALOX15CYP2C19SLC1A3
SCHEMBL21896074 1.00 CYP2D6 (0.47) CYP2D6CYP1A2ALOX15CYP2C19SLC1A3
SCHEMBL9297990 1.00 CYP2D6 (0.47) CYP2D6CYP1A2ALOX15CYP2C19SLC1A3
SCHEMBL3450013 1.00 CYP2D6 (0.47) CYP2D6CYP1A2ALOX15CYP2C19SLC1A3
Hydrochloric Acid SCHEMBL16287994 0.98 CYP1A2 (0.46) CYP2D6CYP1A2ALOX15CYP2C19SLC1A3
Hydrochloric Acid SCHEMBL17600576 0.98 CYP1A2 (0.46) CYP2D6CYP1A2ALOX15CYP2C19SLC1A3
Hydrochloric Acid SCHEMBL16288453 0.98 CYP1A2 (0.46) CYP2D6CYP1A2ALOX15CYP2C19SLC1A3
SCHEMBL2339279 0.86 CYP2D6 (0.44) CYP2D6CYP1A2ALOX15CYP2C19SLC1A3
SCHEMBL13675316 0.86 CYP2D6 (0.44) CYP2D6CYP1A2ALOX15CYP2C19SLC1A3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4628592-A1 PEPTIDE PRODUCTION METHOD COMPRISING STEP FOR TRANSLATING AMINO ACID HAVING OXYGEN ATOM AT SPECIFIC POSITION CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2025-10-08 EP disclosed
US-20250302912-A1 COMPOSITION INCLUDING PEPTIDE COMPOUND AND SURFACTANT CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2025-10-02 US disclosed
US-12415835-B2 Peptide-compound cyclization method CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2025-09-16 US disclosed
US-12410212-B2 Cyclic compound having selective KRAS inhibitory effect on HRAS and NRAS CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2025-09-09 US disclosed
EP-4609875-A2 COMPOSITION CONTAINING PEPTIDE COMPOUND AND SURFACTANT CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2025-09-03 EP disclosed
EP-4603105-A1 PHARMACEUTICAL COMPOSITION CONTAINING CYCLIC COMPOUND HAVING SELECTIVE KRAS INHIBITORY EFFECT AGAINST HRAS AND NRAS CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2025-08-20 EP disclosed
EP-4592308-A1 CYCLIC COMPOUND HAVING SELECTIVE KRAS INHIBITORY EFFECT ON HRAS AND NRAS CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2025-07-30 EP disclosed
US-12371454-B2 Cyclic peptide compound having Kras inhibitory action CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2025-07-29 US disclosed
EP-4166133-B1 COMPOSITION CONTAINING PEPTIDE COMPOUND AND SURFACTANT CHUGAI PHARMACEUTICAL CO LTD (JP) 2025-07-23 EP disclosed
US-20250230193-A1 CYCLIC COMPOUND HAVING SELECTIVE KRAS INHIBITORY EFFECT ON HRAS AND NRAS CHUGAI PHARMACEUTICAL CO LTD (JP) 2025-07-17 US disclosed
EP-2813512-A1 PEPTIDE-COMPOUND CYCLIZATION METHOD Chugai Seiyaku Kabushiki Kaisha (JP) 2014-12-17 EP disclosed
WO-2013100132-A1 PEPTIDE-COMPOUND CYCLIZATION METHOD 中外製薬株式会社 (JP) 2013-07-04 WO disclosed
US-7858741-B2 Stabilization of the collagen triple helix by O-methylation of hydroxyproline residues WISCONSIN ALUMNI RESEARCH FOUNDATION (US) 2010-12-28 US disclosed
US-20090264626-A1 STABILIZATION OF THE COLLAGEN TRIPLE HELIX BY O-METHYLATION OF HYDROXYPROLINE RESIDUES NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2009-10-22 US disclosed
EP-0618810-A4 BRADYKININ ANTAGONIST PEPTIDES. SCIOS NOVA INC (US) 1994-12-07 EP disclosed
EP-0618809-A1 BRADYKININ TYPE PEPTIDES SCIOS NOVA INC. (US) 1994-10-12 EP disclosed
EP-0618810-A1 BRADYKININ ANTAGONIST PEPTIDES SCIOS NOVA INC. (US) 1994-10-12 EP disclosed
EP-0618809-A4 BRADYKININ TYPE PEPTIDES. SCIOS NOVA INC (US) 1994-07-28 EP disclosed
WO-1992018155-A1 BRADYKININ TYPE PEPTIDES NOVA TECHNOLOGY LIMITED PARTNERSHIP (US) 1992-10-29 WO disclosed
US-4316906-A HYPOTENSIVE AGENTS E. R. SQUIBB & SONS, INC. (US) 1982-02-23 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 (6 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-20090264626-A1 STABILIZATION OF THE COLLAGEN TRIPLE HELIX BY O-METHYLATION OF HYDROXYPROLINE RESIDUES COL14A1, COL2A1, PLOD3 CYP2D6 2584/4885CYP1A2 2169/4885ALOX15 3370/4885
US-12410212-B2 Cyclic compound having selective KRAS inhibitory effect on HRAS and NRAS KRAS, HRAS, NRAS CYP2D6 3511/4885CYP1A2 4290/4885ALOX15 4690/4885
US-20250230193-A1 CYCLIC COMPOUND HAVING SELECTIVE KRAS INHIBITORY EFFECT ON HRAS AND NRAS KRAS, HRAS, NRAS CYP2D6 3511/4885CYP1A2 4290/4885ALOX15 4690/4885
US-12371454-B2 Cyclic peptide compound having Kras inhibitory action KRAS, NRAS, HRAS CYP2D6 4576/4885CYP1A2 4845/4885ALOX15 4409/4885
US-20250302912-A1 COMPOSITION INCLUDING PEPTIDE COMPOUND AND SURFACTANT PCTP, CETP, PLTP CYP2D6 4748/4885CYP1A2 4802/4885ALOX15 2520/4885
US-12415835-B2 Peptide-compound cyclization method VIP, NGLY1, GLP1R CYP2D6 4715/4885CYP1A2 4833/4885ALOX15 3621/4885

“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.