SCHEMBL40804

SCHEMBL40804

CC(C)(C)OC(=O)N1CCC[C@H]1C=O

nearest known ligand 0.51

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
HSD17B10 Q99714 1/20 0.49
SMN1; SMN2 Q16637 1/20 0.46
ALDH1A1 P00352 4/20 0.45
NPC1 O15118 1/20 0.43
HPGD P15428 1/20 0.42
MEN1 O00255 3/20 0.42
KMT2A Q03164 3/20 0.42
TSHR P16473 1/20 0.42
L3MBTL1 Q9Y468 1/20 0.42
MAPT P10636 1/20 0.42
LMNA P02545 1/20 0.41
NPSR1 Q6W5P4 1/20 0.41
CTSK P43235 1/20 0.41

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
SCHEMBL338312 1.00 HSD17B10 (0.49) HSD17B10SMN1; SMN2ALDH1A1NPC1HPGD
SCHEMBL190173 1.00 HSD17B10 (0.49) HSD17B10SMN1; SMN2ALDH1A1NPC1HPGD
SCHEMBL2896341 0.95 HSD17B10 (0.45) HSD17B10SMN1; SMN2ALDH1A1NPC1HPGD
SCHEMBL1991179 0.95 HSD17B10 (0.45) HSD17B10SMN1; SMN2ALDH1A1NPC1HPGD
SCHEMBL1991177 0.95 HSD17B10 (0.45) HSD17B10SMN1; SMN2ALDH1A1NPC1HPGD
SCHEMBL14398395 0.94 HPGD (0.47) HSD17B10SMN1; SMN2ALDH1A1NPC1HPGD
SCHEMBL25980668 0.94 HPGD (0.47) HSD17B10SMN1; SMN2ALDH1A1NPC1HPGD
SCHEMBL31336384 0.94 HPGD (0.47) HSD17B10SMN1; SMN2ALDH1A1NPC1HPGD
SCHEMBL9381153 0.90 HSD17B10 (0.57) HSD17B10SMN1; SMN2ALDH1A1NPC1MEN1
SCHEMBL2030521 0.90 HSD17B10 (0.41) HSD17B10SMN1; SMN2ALDH1A1HPGDCTSK

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 1239 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116462622-B Preparation method of N-Boc-L-prolyl 上海药坦药物研究开发有限公司 2024-02-09 CN claimed
CN-116462622-A Preparation method of N-Boc-L-prolyl 上海药坦药物研究开发有限公司 2023-07-21 CN claimed
CN-114920683-A Preparation method of Boc-prolinaldehyde and (R, E) - (1-methylpyrrolidine-2-yl) acrylic acid 苏州富士莱医药股份有限公司 2022-08-19 CN claimed
CN-114602555-A Preparation method and application of chitosan Schiff base immobilized copper material 湖北工程学院 2022-06-10 CN claimed
JP-5025125-A None JP disclosed
CN-116829557-B Pentaheterocycle compound, preparation method and application thereof 上海艾力斯医药科技股份有限公司 2026-05-12 CN disclosed
US-12612414-B2 Nitrile SUMO inhibitors and uses thereof CIT THERAPEUTICS, INC. (US) 2026-04-28 US disclosed
US-20260109696-A1 SMALL MOLECULE PROTEIN SYNTHESIS MODULATORS Interdict Bio, Inc. (US) 2026-04-23 US disclosed
US-20260108619-A1 CONJUGATION LINKERS, CELL BINDING MOLECULE-DRUG CONJUGATES CONTAINING THE LINKERS, METHODS OF MAKING AND USES SUCH CONJUGATES WITH THE LINKERS HANGZHOU DAC BIOTECH CO., LTD. (CN) 2026-04-23 US disclosed
EP-4482583-B1 ZWITTERIONIC ANTIBACTERIAL COMPOUNDS HOFFMANN LA ROCHE (CH) 2026-04-01 EP disclosed
EP-3912979-B1 TYROSINE KINASE INHIBITORS PRINCIPIA BIOPHARMA INC (US) 2026-03-25 EP disclosed
US-20260078116-A1 SMALL MOLECULE PROTEIN SYNTHESIS MODULATORS Interdict Bio, Inc. (US) 2026-03-19 US disclosed
US-5095006-A Enzyme inhibitors BAYER AKTIENGESELLSCHAFT (DE) 1992-03-10 US disclosed
EP-0468469-A2 Proline derivatives Japan Tobacco Inc. (JP) 1992-01-29 EP disclosed
EP-0412350-A2 Renininhibitors, procedure for their preparation and use as medicaments BAYER AG (DE) 1991-02-13 EP disclosed
EP-0384341-A2 New proline derivatives KABUSHIKI KAISHA YAKULT HONSHA (JP) 1990-08-29 EP disclosed
WO-1990004588-A1 HETEROCYCLIC ACETYLENIC AMINES HAVING CENTRAL NERVOUS SYSTEM ACTIVITY THE UPJOHN COMPANY (US) 1990-05-03 WO disclosed
US-4921855-A New Histidyl amino acid derivatives, and pharmaceutical composition comprising the same FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 1990-05-01 US disclosed
EP-0300189-A2 New amino acid derivatives, processes for the preparation thereof and pharmaceutical composition comprising the same FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 1989-01-25 EP disclosed
EP-0207420-A2 Pyridonecarboxylic acid derivatives DAIICHI PHARMACEUTICAL CO., LTD. (JP) 1987-01-07 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-12612414-B2 Nitrile SUMO inhibitors and uses thereof SUMO1, SUMO3, PSMB6 HSD17B10 1332/4885SMN1; SMN2 4141/4885ALDH1A1 1299/4885
US-20260078116-A1 SMALL MOLECULE PROTEIN SYNTHESIS MODULATORS MYC, KRAS, MCL1 HSD17B10 4362/4885SMN1; SMN2 958/4885ALDH1A1 3887/4885
US-20260109696-A1 SMALL MOLECULE PROTEIN SYNTHESIS MODULATORS KRAS, MYC, NRAS HSD17B10 3043/4885SMN1; SMN2 1323/4885ALDH1A1 3241/4885
US-20260108619-A1 CONJUGATION LINKERS, CELL BINDING MOLECULE-DRUG CONJUGATES CONTAINING THE LINKERS, METHODS OF MAKING AND USES SUCH CONJUGATES WITH THE LINKERS DCLRE1A, CCR3, CCR8 HSD17B10 3355/4885SMN1; SMN2 4051/4885ALDH1A1 2641/4885

“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.