SCHEMBL972349

SCHEMBL972349

C=CCN[C@@H](Cc1ccccc1)C(=O)O

nearest known ligand 0.51

Predicted protein targets (top 8)

geneUniProtsupporting neighboursconfidence
MME P08473 2/20 0.50
NPSR1 Q6W5P4 1/20 0.49
FPR2 P25090 5/20 0.48
NAALAD2 Q9Y3Q0 1/20 0.48
CYP1A2 P05177 1/20 0.47
MMP2 P08253 3/20 0.47
MMP9 P14780 2/20 0.47
L3MBTL1 Q9Y468 1/20 0.47

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
SCHEMBL972348 1.00 MME (0.50) MMENPSR1FPR2NAALAD2CYP1A2
Hydrochloric Acid SCHEMBL8133191 0.98 MME (0.49) MMENPSR1FPR2NAALAD2CYP1A2
Hydrochloric Acid SCHEMBL8133188 0.98 MME (0.49) MMENPSR1FPR2NAALAD2CYP1A2
Fluoride SCHEMBL29086588 0.97 MME (0.48) MMENPSR1FPR2NAALAD2CYP1A2
SCHEMBL29086585 0.94 MME (0.46) MMENPSR1FPR2NAALAD2MMP2
1,2-Dichlorobenzene SCHEMBL16428571 0.91 ITGB1 (0.51) MMENPSR1FPR2NAALAD2CYP1A2
SCHEMBL598433 0.87 FOLH1 (0.50) MMENAALAD2L3MBTL1
SCHEMBL9755786 0.87 EPHX1 (0.46) MMP2
SCHEMBL598434 0.87 FOLH1 (0.50) MMENAALAD2L3MBTL1
SCHEMBL9755788 0.87 EPHX1 (0.46) MMP2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2006017619-A2 RECEPTOR-BINDING CYCLIC PEPTIDES AND METHODS OF USE THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2006-02-16 WO claimed
US-20060029544-A1 Receptor-binding cyclic peptides and methods of use THE REGENTS OF THE UNIVERSITY OF CALIFORNIA OFFICE OF TECHNOLOGY TRANSFER (US) 2006-02-09 US claimed
EP-0030847-B1 PHARMACOLOGICALLY ACTIVE PEPTIDES, THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM ELI LILLY AND COMPANY (US) 1984-05-30 EP claimed
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-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-20250230193-A1 CYCLIC COMPOUND HAVING SELECTIVE KRAS INHIBITORY EFFECT ON HRAS AND NRAS CHUGAI PHARMACEUTICAL CO LTD (JP) 2025-07-17 US disclosed
CN-120202211-A Cyclic compounds having selective KRAS inhibition over HRAS and NRAS 中外制药株式会社 2025-06-24 CN disclosed
EP-4512818-A1 CYCLIC COMPOUND HAVING SELECTIVE KRAS INHIBITORY EFFECT ON HRAS AND NRAS Chugai Seiyaku Kabushiki Kaisha (JP) 2025-02-26 EP disclosed
US-20250051394-A1 CYCLIC COMPOUND HAVING SELECTIVE KRAS INHIBITORY EFFECT ON HRAS AND NRAS CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2025-02-13 US disclosed
WO-2024151890-A1 LINKERS, DRUG LINKERS AND CONJUGATES THEREOF AND METHODS OF USING THE SAME PROFOUNDBIO US CO. (US) 2024-07-18 WO disclosed
EP-0119705-A2 Octapeptide vasopressin antagonists SMITHKLINE BECKMAN CORPORATION (US) 1984-09-26 EP disclosed
EP-0030847-B1 PHARMACOLOGICALLY ACTIVE PEPTIDES, THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM ELI LILLY AND COMPANY (US) 1984-05-30 EP disclosed
US-4448972-A Adamantyl containing intermediates SMITHKLINE BECKMAN CORPORATION (US) 1984-05-15 US disclosed
US-4395401-A Renally active dipeptides SMITHKLINE BECKMAN CORPORATION (US) 1983-07-26 US disclosed
US-4395401-A Renally active dipeptides SMITHKLINE BECKMAN CORPORATION (US) 1983-07-26 US disclosed
US-4387049-A Adamantyl containing peptides SMITHKLINE BECKMAN CORPORATION (US) 1983-06-07 US disclosed
EP-0074787-A1 Renally active dipeptides SMITHKLINE BECKMAN CORPORATION (US) 1983-03-23 EP disclosed
EP-0074787-A1 Renally active dipeptides SMITHKLINE BECKMAN CORPORATION (US) 1983-03-23 EP disclosed
EP-0030847-A2 Pharmacologically active peptides, their preparation and pharmaceutical compositions containing them ELI LILLY AND COMPANY (US) 1981-06-24 EP 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 (4 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-12410212-B2 Cyclic compound having selective KRAS inhibitory effect on HRAS and NRAS KRAS, HRAS, NRAS MME 2449/4885NPSR1 4714/4885FPR2 3678/4885
US-20250051394-A1 CYCLIC COMPOUND HAVING SELECTIVE KRAS INHIBITORY EFFECT ON HRAS AND NRAS KRAS, HRAS, NRAS MME 2449/4885NPSR1 4714/4885FPR2 3678/4885
US-20060029544-A1 Receptor-binding cyclic peptides and methods of use ITGB3, ITGB5, ITGA5 MME 3723/4885NPSR1 372/4885FPR2 115/4885
US-20250230193-A1 CYCLIC COMPOUND HAVING SELECTIVE KRAS INHIBITORY EFFECT ON HRAS AND NRAS KRAS, HRAS, NRAS MME 2449/4885NPSR1 4714/4885FPR2 3678/4885

“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.