SCHEMBL27774

SCHEMBL27774

CCOC(=O)C1CCN(c2ccc([N+](=O)[O-])cc2)CC1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
MAPT P10636 8/20 1.00
ALDH1A1 P00352 7/20 0.67
SMN1; SMN2 Q16637 2/20 0.67
LMNA P02545 1/20 0.67
KMT2A Q03164 2/20 0.65
GAA P10253 1/20 0.65
LGMN Q99538 2/20 0.61
TDP1 Q9NUW8 1/20 0.59
POLB P06746 1/20 0.58
HTT P42858 2/20 0.56
TP53 P04637 2/20 0.56

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
SCHEMBL17888540 0.88 MAPT (0.79) MAPTALDH1A1SMN1; SMN2LMNAKMT2A
SCHEMBL25845895 0.88 MAPT (0.78) MAPTALDH1A1SMN1; SMN2LMNAKMT2A
SCHEMBL2662096 0.85 MAPT (0.74) MAPTALDH1A1KMT2AGAALGMN
SCHEMBL21848210 0.85 MAPT (0.74) MAPTALDH1A1SMN1; SMN2LMNAKMT2A
SCHEMBL596038 0.85 MAPT (1.00) MAPTALDH1A1SMN1; SMN2LMNAKMT2A
SCHEMBL16969266 0.84 MAPT (0.73) MAPTALDH1A1SMN1; SMN2LMNAKMT2A
SCHEMBL15850037 0.84 MAPT (0.71) MAPTALDH1A1SMN1; SMN2LMNAKMT2A
SCHEMBL25584267 0.83 MAPT (0.71) MAPTALDH1A1SMN1; SMN2LMNAKMT2A
SCHEMBL5726280 0.83 MAPT (0.71) MAPTALDH1A1SMN1; SMN2LMNAKMT2A
SCHEMBL4399969 0.82 MAPT (0.70) MAPTALDH1A1SMN1; SMN2LMNAKMT2A

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-20260092057-A1 BCL-XL/BCL-2 DEGRADERS AND USES THEREOF KYMERA THERAPEUTICS INC (US) 2026-04-02 US disclosed
EP-4522154-A1 BCL-XL/BCL-2 DEGRADERS AND USES THEREOF Kymera Therapeutics, Inc. (US) 2025-03-19 EP disclosed
WO-2023220425-A1 BCL-XL/BCL-2 DEGRADERS AND USES THEREOF KYMERA THERAPEUTICS, INC. (US) 2023-11-16 WO disclosed
US-9249163-B2 PDE10a inhibitors for the treatment of type II diabetes JANSSEN PHARMACEUTICA NV. (BE) 2016-02-02 US disclosed
US-9249163-B2 PDE10a inhibitors for the treatment of type II diabetes JANSSEN PHARMACEUTICA NV. (BE) 2016-02-02 US disclosed
EP-2407466-B1 PIPERAZINE COMPOUND CAPABLE OF INHIBITING PROSTAGLANDIN D SYNTHASE TAIHO PHARMACEUTICAL CO LTD (JP) 2016-01-13 EP disclosed
US-9193736-B2 PDE 10a inhibitors for the treatment of type II diabetes JANSSEN PHARMACEUTICA, NV (BE) 2015-11-24 US disclosed
US-9193736-B2 PDE 10a inhibitors for the treatment of type II diabetes JANSSEN PHARMACEUTICA, NV (BE) 2015-11-24 US disclosed
US-9062035-B2 Piperazine compound capable of inhibiting prostaglandin D synthase TAIHO PHARMACEUTICAL CO., LTD. (JP) 2015-06-23 US disclosed
US-20140364413-A1 PDE 10a Inhibitors for the Treatment of Type II Diabetes JANSSEN PHARMACEUTICA, NV (BE) 2014-12-11 US disclosed
EP-2378878-A1 INHIBITORS OF DIACYLGLYCEROL ACYLTRANSFERASE Via Pharmaceuticals, Inc. (US) 2011-10-26 EP disclosed
WO-2010077861-A1 INHIBITORS OF DIACYLGLYCEROL ACLYTRANSFERASE VIA PHARMACEUTICALS, INC (US) 2010-07-08 WO disclosed
US-20100152445-A1 Inhibitors of Diacylglycerol Acyltransferase MADRIGAL PHARMACEUTICALS, INC. 2010-06-17 US disclosed
US-20090291945-A1 CYSTEINE PROTEASE INHIBITORS TEIJIN PHARMA LIMITED (JP) 2009-11-26 US disclosed
US-20090291945-A1 CYSTEINE PROTEASE INHIBITORS TEIJIN PHARMA LIMITED (JP) 2009-11-26 US disclosed
WO-2009029998-A1 RETROMETABOLIC COMPOUNDS CYTOPIA RESEARCH PTY LTD (AU) 2009-03-12 WO disclosed
US-20070249620-A1 Urea Derivative SANKYO COMPANY, LIMITED (JP) 2007-10-25 US disclosed
US-20070099934-A1 N-aryl piperidine substituted biphenylcarboxamides as inhibitors of apolipoprotein b JANSSEN PHARMACEUTICA N.V. (BE) 2007-05-03 US disclosed
US-20070099934-A1 N-aryl piperidine substituted biphenylcarboxamides as inhibitors of apolipoprotein b JANSSEN PHARMACEUTICA N.V. (BE) 2007-05-03 US disclosed
EP-1764360-A1 UREA DERIVATIVE Sankyo Company, Limited (JP) 2007-03-21 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 (6 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-20140364413-A1 PDE 10a Inhibitors for the Treatment of Type II Diabetes PDE2A, PDE3B, PDE3A MAPT 4646/4885ALDH1A1 381/4885SMN1; SMN2 3681/4885
US-20090291945-A1 CYSTEINE PROTEASE INHIBITORS CTSE, SPINT2, CTSF MAPT 480/4885ALDH1A1 2506/4885SMN1; SMN2 4525/4885
US-20100152445-A1 Inhibitors of Diacylglycerol Acyltransferase DGAT2, DGAT1, ACAT2 MAPT 3731/4885ALDH1A1 1249/4885SMN1; SMN2 4770/4885
US-20070099934-A1 N-aryl piperidine substituted biphenylcarboxamides as inhibitors of apolipoprotein b APOB, PNLIP, LIPC MAPT 4151/4885ALDH1A1 909/4885SMN1; SMN2 3217/4885
US-20260092057-A1 BCL-XL/BCL-2 DEGRADERS AND USES THEREOF BCL2L2, BCL2A1, BCL2L1 MAPT 4734/4885ALDH1A1 1304/4885SMN1; SMN2 744/4885
US-20070249620-A1 Urea Derivative UGP2, SLC14A1, DGAT1 MAPT 758/4885ALDH1A1 731/4885SMN1; SMN2 4424/4885

“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.