SCHEMBL65167

SCHEMBL65167

O=C(O)C1(c2ccccc2)CCCC1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
AKR1C1 Q04828 1/20 1.00
HDAC4 P56524 2/20 0.66
KMT2A Q03164 4/20 0.59
MEN1 O00255 2/20 0.59
SMN1; SMN2 Q16637 3/20 0.56
HTT P42858 2/20 0.56
LMNA P02545 2/20 0.54
NPSR1 Q6W5P4 2/20 0.54
L3MBTL1 Q9Y468 1/20 0.54
TET3 O43151 1/20 0.54
FBXL19 Q6PCT2 1/20 0.54
CXXC5 Q7LFL8 1/20 0.54
TET1 Q8NFU7 1/20 0.54
KDM2B Q8NHM5 1/20 0.54
CXXC4 Q9H2H0 1/20 0.54
KDM2A Q9Y2K7 1/20 0.54
HSD11B1 P28845 2/20 0.53
TSHR P16473 1/20 0.53
ALDH1A1 P00352 1/20 0.51

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
SCHEMBL1041902 0.98 AKR1C1 (0.96) AKR1C1HDAC4KMT2AMEN1SMN1; SMN2
SCHEMBL19249602 0.98 AKR1C1 (0.96) AKR1C1HDAC4KMT2AMEN1SMN1; SMN2
SCHEMBL1042420 0.98 AKR1C1 (0.96) AKR1C1HDAC4KMT2AMEN1SMN1; SMN2
SCHEMBL66387 0.98 AKR1C1 (0.96) AKR1C1HDAC4KMT2AMEN1SMN1; SMN2
Hydrochloric Acid SCHEMBL8315894 0.98 AKR1C1 (0.96) AKR1C1HDAC4KMT2AMEN1SMN1; SMN2
SCHEMBL3811046 0.96 AKR1C1 (0.92) AKR1C1HDAC4KMT2AMEN1SMN1; SMN2
SCHEMBL1667343 0.95 AKR1C1 (0.91) AKR1C1HDAC4KMT2AMEN1SMN1; SMN2
Water SCHEMBL3811044 0.94 AKR1C1 (0.88) AKR1C1HDAC4KMT2AMEN1SMN1; SMN2
Hydrochloric Acid SCHEMBL8105149 0.93 AKR1C1 (0.88) AKR1C1HDAC4KMT2AMEN1SMN1; SMN2
SCHEMBL11665752 0.93 AKR1C1 (0.88) AKR1C1HDAC4KMT2AMEN1SMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122094387-A Perovskite film based on volatile additive, and preparation method and application thereof 2026-05-26 CN claimed
EP-4661890-A1 PTP1B/TC-PTP DUAL INHIBITORS AND PROTEIN DEGRADERS Purdue Research Foundation (US) 2025-12-17 EP claimed
CN-118771956-A Carboxylic acid decarboxylation coupling conversion method using sulfur hexafluoride as oxidizing reagent 国网安徽省电力有限公司电力科学研究院 2024-10-15 CN claimed
WO-2024167565-A1 PTP1B/TC-PTP DUAL INHIBITORS AND PROTEIN DEGRADERS PURDUE RESEARCH FOUNDATION (US) 2024-08-15 WO claimed
CN-117623949-A Preparation method of pentovirine citrate 苏州敬业医药化工有限公司 2024-03-01 CN claimed
CN-114388761-A Lithium battery negative electrode material and preparation method thereof 曾福强 2022-04-22 CN claimed
EP-3104847-B1 NOVEL USE OF SIGMA-1 RECEPTOR AGONIST COMPOUNDS MTA TAMOGATOTT KUTATOCSOPORTOK IRODAJA (HU) 2020-11-11 EP claimed
CN-108623814-B Copper-based porous coordination polymer hydrogen storage material and preparation method thereof 中国石油化工股份有限公司 2020-10-16 CN claimed
CN-108912713-A A kind of energy conservation and environmental protection plastic and preparation method thereof 合肥万之景门窗有限公司 2018-11-30 CN claimed
CN-108623814-A A kind of copper-based Porous coordination polymer hydrogen storage material and preparation method thereof 中国石油化工股份有限公司 2018-10-09 CN claimed
US-20050090690-A1 Process for preparing tetra-amide compounds XEROX CORPORATION 2005-04-28 US claimed
WO-2004089416-A2 COMBINATION OF AN 11BETA-HYDROXYSTEROID DEHYDROGENASE TYPE 1 INHIBITOR AND AN ANTIHYPERTENSIVE AGENT NOVO NORDISK A/S (DK) 2004-10-21 WO claimed
WO-2004089470-A2 NEW AMIDE DERIVATIVES AND PHARMACEUTICAL USE THEREOF NOVO NORDISK A/S (DK) 2004-10-21 WO claimed
WO-2004089415-A2 COMBINATIONS OF AN 11β-HYDROXYSTEROID DEHYDROGENASE TYPE 1 INHIBITOR AND A GLUCOCORTICOID RECEPTOR AGONIST NOVO NORDISK A/S (DK) 2004-10-21 WO claimed
US-6323243-B1 AROMATIC ETHER WITH AMINE OR AMIDE GROUPS WARNER-LAMBERT COMPANY 2001-11-27 US claimed
WO-2000006535-A1 TYROSINE-DERIVED COMPOUNDS AS CALCIUM CHANNEL ANTAGONISTS WARNER-LAMBERT COMPANY (US) 2000-02-10 WO claimed
US-4686302-A Simultaneous preparation of nitriles and acrylamide or methacrylamide BASF AKTIENGESELLSCHAFT (DE) 1987-08-11 US claimed
EP-0081756-B1 NEW COMPOUNDS WITH ANTIINFLAMMATORY AND ANTITUSSIVE ACTIVITY, PROCESS FOR THEIR PREPARATION AND RELATIVE PHARMACEUTICAL COMPOSITIONS MEDEA RESEARCH S.r.l. (IT) 1985-05-15 EP claimed
EP-0081756-A1 New compounds with antiinflammatory and antitussive activity, process for their preparation and relative pharmaceutical compositions MEDEA RESEARCH S.r.l. (IT) 1983-06-22 EP claimed
EP-0024172-B1 ANTITUMOR AND IMMUNOSUPPRESSIVE 4-CARBAMOYLIMIDAZOLIUM-5-OLATE DERIVATIVES, PHARMACEUTICAL COMPOSITION AND PRODUCTION THEREOF SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1983-05-11 EP 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 (1 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-20050090690-A1 Process for preparing tetra-amide compounds TAF9, TAF5, TAF1 AKR1C1 2446/4885HDAC4 802/4885KMT2A 826/4885

“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.