SCHEMBL29553

SCHEMBL29553

O=C(O)[C@@H]1CCCN1C(=O)OCc1ccccc1

nearest known ligand 0.70

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
PREP P48147 3/20 0.67
ALDH1A1 P00352 3/20 0.63
SMN1; SMN2 Q16637 1/20 0.63
CTRB1 P17538 1/20 0.63
NPSR1 Q6W5P4 1/20 0.61
TSHR P16473 2/20 0.60
L3MBTL1 Q9Y468 1/20 0.60
KMT2A Q03164 1/20 0.60
KLK7 P49862 1/20 0.60
KLK5 Q9Y337 1/20 0.60
KDM4E B2RXH2 1/20 0.60
LMNA P02545 1/20 0.60
GFER P55789 1/20 0.59
HSD17B10 Q99714 1/20 0.59

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
SCHEMBL475715 1.00 PREP (0.67) PREPALDH1A1SMN1; SMN2CTRB1NPSR1
SCHEMBL29658848 1.00 PREP (0.67) PREPALDH1A1SMN1; SMN2CTRB1NPSR1
SCHEMBL205223 1.00 PREP (0.67) PREPALDH1A1SMN1; SMN2CTRB1NPSR1
Hydrochloric Acid SCHEMBL32677508 0.99 PREP (0.65) PREPALDH1A1SMN1; SMN2CTRB1NPSR1
SCHEMBL630208 0.96 PREP (0.62) PREPALDH1A1SMN1; SMN2CTRB1NPSR1
SCHEMBL82714 0.96 PREP (0.62) PREPALDH1A1SMN1; SMN2CTRB1NPSR1
SCHEMBL630241 0.96 PREP (0.62) PREPALDH1A1SMN1; SMN2CTRB1NPSR1
SCHEMBL18093534 0.95 PREP (0.71) PREPALDH1A1SMN1; SMN2CTRB1NPSR1
SCHEMBL20678314 0.95 PREP (0.71) PREPALDH1A1SMN1; SMN2CTRB1NPSR1
SCHEMBL17459415 0.95 PREP (0.71) PREPALDH1A1SMN1; SMN2CTRB1NPSR1

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 1412 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250100999-A1 METHODS AND INTERMEDIATES FOR PREPARING THERAPEUTIC COMPOUNDS GILEAD SCIENCES, INC. 2025-03-27 US claimed
CN-119490446-A Synthesis method of important intermediate (S) -2-Boc-aminomethylpyrrolidine of levo-sulpride 苏州艾缇克药物化学有限公司 2025-02-21 CN claimed
CN-119423091-A Environment-friendly pesticide based on hexazinone and preparation method thereof 江苏禾裕泰化学有限公司 2025-02-14 CN claimed
CN-119285609-A Preparation method of chiral 6-methyl nicotine 恒信永基科技(深圳)有限公司 2025-01-10 CN claimed
CN-118406404-A Circuit board ink-jet printing ink stripping agent and preparation method and application thereof 珠海市板明科技有限公司 2024-07-30 CN claimed
CN-114998621-B SERS quantitative analysis method based on coffee ring concentration effect and image processing technology 嘉兴学院 2024-04-16 CN claimed
CN-117721474-A Cleaning agent for chip after chemical mechanical polishing, preparation method and application thereof 江苏奥首材料科技有限公司 2024-03-19 CN claimed
CN-113929736-B Gly-Pro-Arg-Pro-oxaminocarbonyl warfarin, synthesis, activity and application thereof 首都医科大学 2024-01-26 CN claimed
EP-4253366-A2 METHODS AND INTERMEDIATES FOR PREPARING A THERAPEUTIC COMPOUND USEFUL IN THE TREATMENT OF RETROVIRIDAE VIRAL INFECTION Gilead Sciences, Inc. (US) 2023-10-04 EP claimed
US-11760746-B2 Methods and intermediates for preparing therapeutic compounds GILEAD SCIENCES, INC. (US) 2023-09-19 US claimed
EP-0817795-B1 NOVEL 4-SUBSTITUTED-3-PEPTIDYL-AZETIDIN-2-ONE DERIVATIVES USEFUL AS CYSTEINE PROTEINASE INHIBITOR NAEJA PHARMACEUTICAL INC (CA) 2000-11-15 EP claimed
EP-0817795-A1 NOVEL 4-SUBSTITUTED-3-PEPTIDYL-AZETIDIN-2-ONE DERIVATIVES USEFUL AS CYSTEINE PROTEINASE INHIBITOR SYNPHAR LABORATORIES INC. (CA) 1998-01-14 EP claimed
WO-1996032408-A1 NOVEL 4-SUBSTITUTED-3-PEPTIDYL-AZETIDIN-2-ONE DERIVATIVES USEFUL AS CYSTEINE PROTEINASE INHIBITOR SYNPHAR LABORATORIES, INC. (US) 1996-10-17 WO claimed
US-5221752-A Inhibits prolyl endopeptidase activity; active ingredient of an enzyme inhibitor NIPPON KAYAKU KABUSHIKI KAISHA (JP) 1993-06-22 US claimed
EP-0384341-A2 New proline derivatives KABUSHIKI KAISHA YAKULT HONSHA (JP) 1990-08-29 EP claimed
EP-0322765-A2 New thiazolidine derivatives, process for preparing same and anti-amnestic composition containing same KABUSHIKI KAISHA YAKULT HONSHA (JP) 1989-07-05 EP claimed
US-4434095-A Cyclic analogue of naturally-occurring phagocytosis-stimulant peptide - threonyl-cyclo-[-N.sup.ε -lysyl-prolyl-arginyl] INSTITUTE ORGANICHESKOGO SINTEZA (SU) 1984-02-28 US claimed
US-RE30496-E Tripeptide derivatives with central nervous system activity and preparation thereof AYERST, MCKENNA & HARRISON, LTD. (CA) 1981-01-27 US claimed
US-4085207-A AND AT LEAST ONE OF N-ACYL-L-TRYPTOPHANS AND N-ACYL-L-PROLINES OTSUKA PHARMACEUTICAL FACTORY, INC. (JA) 1978-04-18 US claimed
US-4018912-A Tripeptide derivatives with central nervous system activity and preparation thereof AYERST MCKENNA AND HARRISON LTD. (CA) 1977-04-19 US claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 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-20250100999-A1 METHODS AND INTERMEDIATES FOR PREPARING THERAPEUTIC COMPOUNDS CYP11A1, CYP11B1, CYP11B2 PREP 1315/4885ALDH1A1 1161/4885SMN1; SMN2 592/4885
US-11760746-B2 Methods and intermediates for preparing therapeutic compounds CYP11A1, CYP11B1, CYP11B2 PREP 1427/4885ALDH1A1 1151/4885SMN1; SMN2 628/4885

“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.