SCHEMBL1010332

SCHEMBL1010332

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

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
RAB9A P51151 1/20 1.00
HTT P42858 1/20 0.55
TSHR P16473 2/20 0.54
ALDH1A1 P00352 2/20 0.54
GAA P10253 1/20 0.54
ACE P12821 6/20 0.54
REN P00797 4/20 0.54
KDM4E B2RXH2 1/20 0.54
F2 P00734 1/20 0.54
LMNA P02545 1/20 0.54
LTA4H P09960 1/20 0.54
MAPT P10636 1/20 0.54
PEPD P12955 1/20 0.54
ALOX15 P16050 1/20 0.54
PTGS1 P23219 1/20 0.54
HTR2A P28223 1/20 0.54
PTGS2 P35354 1/20 0.54
HRH1 P35367 1/20 0.54
THPO P40225 1/20 0.54
PMP22 Q01453 1/20 0.54

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
SCHEMBL1010333 1.00 RAB9A (1.00) RAB9AHTTTSHRALDH1A1GAA
SCHEMBL1012705 1.00 RAB9A (1.00) RAB9AHTTTSHRALDH1A1GAA
SCHEMBL21225551 0.95 RAB9A (0.91) RAB9AHTTTSHRALDH1A1GAA
SCHEMBL21241511 0.95 RAB9A (0.91) RAB9AHTTTSHRALDH1A1GAA
SCHEMBL18190844 0.90 RAB9A (0.82) RAB9AHTTTSHRALDH1A1GAA
SCHEMBL7877696 0.90 RAB9A (0.82) RAB9AHTTTSHRALDH1A1GAA
SCHEMBL3680005 0.88 RAB9A (0.78) RAB9AHTTTSHRALDH1A1GAA
SCHEMBL3680002 0.88 RAB9A (0.78) RAB9AHTTTSHRALDH1A1GAA
SCHEMBL15148125 0.85 RAB9A (0.74) RAB9AHTTTSHRALDH1A1GAA
SCHEMBL8544043 0.84 RAB9A (0.72) RAB9AHTTTSHRALDH1A1GAA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20020037559-A1 PROCESS FOR PRODUCING N-PROTECTED D-PROLINE DERIVATIVES LONZA A.G. (CH) 2002-03-28 US claimed
EP-0896617-A1 PROCESS FOR PRODUCING N-PROTECTED D-PROLINE DERIVATIVES LONZA AG (CH) 1999-02-17 EP claimed
WO-1997033987-A1 PROCESS FOR PRODUCING N-PROTECTED D-PROLINE DERIVATIVES LONZA AG (CH) 1997-09-18 WO claimed
EP-4139295-B1 ISOQUINILINE NRF2 AGONISTS C4X DISCOVERY LTD (GB) 2025-04-09 EP disclosed
EP-1824876-B1 PANCREATIC POLYPEPTIDE FAMILY MOTIFS, POLYPEPTIDES AND METHODS COMPRISING THE SAME AMYLIN PHARMACEUTICALS LLC (US) 2015-07-29 EP disclosed
US-8012963-B2 3,4-dihydro-2H-benzo[1,4]oxazine and thiazine derivatives as CETP inhibitors JANSSEN PHARMACEUTICA N.V. (BE) 2011-09-06 US disclosed
US-20110212956-A1 Pyrazolopyrimidines for treating CNS disorders MERZ PHARMA GMBH & CO. KGAA (DE) 2011-09-01 US disclosed
US-7985753-B2 Substituted pyrazolo[1,5-A]pyrimidines as metabotropic glutamate receptor modulators MERZ PHARMA GMBH & CO. KGAA (DE) 2011-07-26 US disclosed
EP-2295439-A1 Substituted pyrazolopyrimidines, a process for their preparation and their use as medicine Merz Pharma GmbH & Co. KGaA (DE) 2011-03-16 EP disclosed
EP-2054416-B1 SUBSTITUTED PYRAZOLOPYRIMIDINES, A PROCESS FOR THEIR PREPARATION AND THEIR USE AS MEDICINE MERZ PHARMA GMBH & CO KGAA (DE) 2011-01-05 EP disclosed
US-20100227857-A1 3,4-DIHYDRO-2H-BENZO[1,4]OXAZINE AND THIAZINE DERIVATIVES AS CETP INHIBITORS KUO GEE-HONG 2010-09-09 US disclosed
EP-1758866-A1 PROCESSES FOR PREPARING 6-ALKYL-5-ARYLSULFONYL- DIHYDROPHENANTHRIDINES Wyeth (US) 2007-03-07 EP disclosed
US-20060025436-A1 Processes for preparing 6-alkyl-5-arylsulfonyl-dihydrophenanthridines WYETH (US) 2006-02-02 US disclosed
WO-2006009831-A1 PROCESSES FOR PREPARING 6-ALKYL-5-ARYLSULFONYL- DIHYDROPHENANTHRIDINES WYETH (US) 2006-01-26 WO disclosed
US-20020037559-A1 PROCESS FOR PRODUCING N-PROTECTED D-PROLINE DERIVATIVES LONZA A.G. (CH) 2002-03-28 US disclosed
EP-0896617-A1 PROCESS FOR PRODUCING N-PROTECTED D-PROLINE DERIVATIVES LONZA AG (CH) 1999-02-17 EP disclosed
WO-1997033987-A1 PROCESS FOR PRODUCING N-PROTECTED D-PROLINE DERIVATIVES LONZA AG (CH) 1997-09-18 WO disclosed
EP-0273399-B1 Optically active 2,3-dihydrobenzoaxine derivatives and process for preparing the same DAIICHI SEIYAKU CO (JP) 1994-08-17 EP disclosed
US-4895944-A BACTERICIDE OFLOXACIN DAIICHI SEIYAKU COMPANY, LTD. (JP) 1990-01-23 US disclosed
EP-0273399-A1 Optically active 2,3-dihydrobenzoaxine derivatives and process for preparing the same DAIICHI PHARMACEUTICAL CO., LTD. (JP) 1988-07-06 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 (3 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-20100227857-A1 3,4-DIHYDRO-2H-BENZO[1,4]OXAZINE AND THIAZINE DERIVATIVES AS CETP INHIBITORS CETP, MTTP, CES1 RAB9A 4606/4885HTT 3883/4885TSHR 4323/4885
US-20060025436-A1 Processes for preparing 6-alkyl-5-arylsulfonyl-dihydrophenanthridines QDPR, RPS9, RPS4Y1 RAB9A 99/4885HTT 513/4885TSHR 992/4885
US-20110212956-A1 Pyrazolopyrimidines for treating CNS disorders GRM5, GRM3, GRM1 RAB9A 1347/4885HTT 1894/4885TSHR 609/4885

“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.