SCHEMBL13445

SCHEMBL13445

CC(C)(C)OC(=O)N1CCCCC1

nearest known ligand 0.71

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
HPGD P15428 1/20 0.71
SMN1; SMN2 Q16637 2/20 0.62
USP2 O75604 1/20 0.62
EPHX1 P07099 1/20 0.57
MEN1 O00255 2/20 0.53
KMT2A Q03164 2/20 0.53
MAPT P10636 3/20 0.50
PREP P48147 2/20 0.50
ALDH1A1 P00352 2/20 0.50
ABL1 P00519 1/20 0.50
RIN1 Q13671 1/20 0.50
RECQL P46063 1/20 0.49
NPC1 O15118 1/20 0.47
HTT P42858 1/20 0.47
RAB9A P51151 1/20 0.47
EPHX2 P34913 1/20 0.46
CTSK P43235 1/20 0.46
POLB P06746 1/20 0.45

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
SCHEMBL3830876 1.00 HPGD (0.71) HPGDSMN1; SMN2USP2EPHX1MEN1
SCHEMBL19864905 1.00 HPGD (0.71) HPGDSMN1; SMN2USP2EPHX1MEN1
SCHEMBL2077166 1.00 HPGD (0.71) HPGDSMN1; SMN2USP2EPHX1MEN1
SCHEMBL18432213 1.00 HPGD (0.71) HPGDSMN1; SMN2USP2EPHX1MEN1
SCHEMBL19864899 1.00 HPGD (0.71) HPGDSMN1; SMN2USP2EPHX1MEN1
SCHEMBL19852529 1.00 HPGD (0.71) HPGDSMN1; SMN2USP2EPHX1MEN1
SCHEMBL18097955 1.00 HPGD (0.71) HPGDSMN1; SMN2USP2EPHX1MEN1
SCHEMBL60470 1.00 HPGD (0.71) HPGDSMN1; SMN2USP2EPHX1MEN1
SCHEMBL21707988 1.00 HPGD (0.71) HPGDSMN1; SMN2USP2EPHX1MEN1
Ammonia Solution, Strong SCHEMBL20236062 0.98 HPGD (0.69) HPGDSMN1; SMN2USP2EPHX1MEN1

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

Appears in 4530 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260048071-A1 12-LIPOXYGENASE INHIBITORS FOR THE TREATMENT OF LUPUS Cadrenal Therapeutics, Inc. 2026-02-19 US claimed
US-20260027123-A1 Compositions for Modulating Lipoxygenase and Methods of Using Same UNIV CALIFORNIA (US) 2026-01-29 US claimed
EP-4615432-A2 12-LIPOXYGENASE INHIBITORS FOR THE TREATMENT OF LUPUS Veralox Therapeutics Inc. (US) 2025-09-17 EP claimed
EP-4612135-A1 ORAL PHARMACEUTICAL FORMULATIONS CONTAINING 4-((2-HYDROXY-3-METHOXYBENZYL)AMINO) BENZENESULFONAMIDE DERIVATIVES Veralox Therapeutics Inc. (US) 2025-09-10 EP claimed
EP-4558508-A1 COMPOSITIONS FOR MODULATING LIPOXYGENASE AND METHODS OF USING SAME The Regents of the University of California (US) 2025-05-28 EP claimed
CN-116478143-B Donepezil derivative, preparation method and application thereof 山东第一医科大学(山东省医学科学院) 2025-05-09 CN claimed
CN-119899173-A Preparation method of ceritinib as toxic impurity nitrosoceritinib of ceritinib gene 南京亿华药业有限公司 2025-04-29 CN claimed
CN-117229205-B Preparation method and pharmaceutical application of phenyl acrylamide RHbDD1 inhibitor 中国医学科学院基础医学研究所 2025-03-21 CN claimed
CN-119490451-A Compounds as positive modulators of calcium activated chloride channels TMEM16A有限公司 2025-02-21 CN claimed
CN-113924146-B Novel compounds and pharmaceutical compositions thereof for the treatment of diseases 加拉帕戈斯股份有限公司 2024-12-10 CN claimed
EP-1434782-A2 2-PROPYNYL ADENOSINE ANALOGS HAVING A2A AGONIST ACTIVITY AND COMPOSITIONS THEREOF University of Virginia Patent Foundation (US) 2004-07-07 EP claimed
EP-0935465-B1 NOVEL SUBSTITUTED IMIDAZOLE COMPOUNDS SMITHKLINE BEECHAM CORP (US) 2004-04-14 EP claimed
US-20030186926-A1 2-propynyl adenosine analogs having A2A agonist activity and compositions thereof NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2003-10-02 US claimed
WO-2003080125-A2 BENZIMIDAZOLES AND THEIR USE AS MITOGEN-ACTIVATED- AND RHO-KINASE INHIBITORS GLAXO GROUP LIMITED (GB) 2003-10-02 WO claimed
WO-2003045950-A1 PYRAZOLOPYRIDINE DERIVTIVES AND THEIR PHARMACEUTICAL USE FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 2003-06-05 WO claimed
CN-1420881-A Beta-amino acid derivs. as inhibitors of matrix metalloproteases and TNF-alpha BRISTOL MYERS SQUIBB PHARMACEU (US) 2003-05-28 CN claimed
WO-2003029264-A2 2-PROPYNYL ADENOSINE ANALOGS HAVING A2A AGONIST ACTIVITY AND COMPOSITIONS THEREOF UNIVERSITY OF VIRGINIA PATENT FOUNDATION (US) 2003-04-10 WO claimed
US-20020198252-A1 Process for the preparation of alkylamine substituted indoles PAYACK JOSEPH (US) 2002-12-26 US claimed
US-6214844-B1 ANTIARTHRITIC AGENTS; BONE DISORDERS; ANTIINFLAMMATORY AGENTS SMITHKLINE BEECHAM CORPORATION 2001-04-10 US claimed
US-5977103-A Substituted imidazole compounds SMITHKLINE BEECHAM CORPORATION (US) 1999-11-02 US claimed