SCHEMBL4025898

SCHEMBL4025898

O=C(N[C@@H]1CCCc2c1[nH]c1ccc(Cl)cc21)c1ccccn1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
DHODH Q02127 1/20 1.00
ALOX15 P16050 4/20 0.67
SMN1; SMN2 Q16637 3/20 0.67
MAPT P10636 3/20 0.67
MAPK1 P28482 1/20 0.67
MEN1 O00255 3/20 0.58
KMT2A Q03164 3/20 0.58
GLA P06280 1/20 0.58
SIRT1 Q96EB6 9/20 0.54
SIRT2 Q8IXJ6 3/20 0.53
SIRT3 Q9NTG7 2/20 0.53
BRD3 Q15059 3/20 0.51
LMNA P02545 2/20 0.49
TSHR P16473 1/20 0.49
TP53 P04637 1/20 0.49
CRBN Q96SW2 1/20 0.47

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
SCHEMBL4022761 1.00 DHODH (1.00) DHODHALOX15SMN1; SMN2MAPTMAPK1
SCHEMBL4025228 1.00 DHODH (1.00) DHODHALOX15SMN1; SMN2MAPTMAPK1
SCHEMBL30338397 1.00 DHODH (1.00) DHODHALOX15SMN1; SMN2MAPTMAPK1
SCHEMBL24727760 0.91 DHODH (0.84) DHODHALOX15SMN1; SMN2MAPTMAPK1
SCHEMBL4022932 0.89 DHODH (0.80) DHODHALOX15SMN1; SMN2MAPTMAPK1
SCHEMBL4254861 0.88 DHODH (0.79) DHODHALOX15SMN1; SMN2MAPTMAPK1
SCHEMBL31120774 0.87 DHODH (0.76) DHODHALOX15SMN1; SMN2MAPTMAPK1
SCHEMBL4022138 0.86 DHODH (0.75) DHODHALOX15SMN1; SMN2MAPTMAPK1
SCHEMBL4023145 0.85 DHODH (0.74) DHODHALOX15SMN1; SMN2MAPTMAPK1
SCHEMBL4022078 0.85 DHODH (0.74) DHODHALOX15SMN1; SMN2MAPTMAPK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240245664-A1 METHODS OF USING USP15 INHIBITORS THE CURATORS OF THE UNIVERSITY OF MISSOURI 2024-07-25 US claimed
WO-2023039405-A1 METHODS OF USING USP15 INHIBITORS THE CURATORS OF THE UNIVERSITY OF MISSOURI (US) 2023-03-16 WO claimed
US-20220280513-A1 ENHANCING THE ANTIVIRAL EFFICACY OF RNA VIRUS INHIBITION BY COMBINATION WITH MODULATORS OF PYRIMIDINE METABOLISM THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY 2022-09-08 US claimed
WO-2022167402-A1 METHODS OF THERAPY COMPRISING ADMINISTERING A THERAPEUTICALLY EFFECTIVE COMBINATION COMPRISING A DHODH INHIBITOR AND AN IDH INHIBITOR INSERM (Institut National de la Santé et de la Recherche Médicale) (FR) 2022-08-11 WO claimed
EP-1646610-B1 TETRAHYDROCARBAZOLE DERIVATIVES AND THEIR PHARMACEUTICAL USE SMITHKLINE BEECHAM CORP (US) 2009-07-22 EP claimed
US-7419997-B2 Tetrahydrocarbazole derivatives and their pharmaceutical use SMITHKLINE BEECHAM CORPORATION (US) 2008-09-02 US claimed
US-20060148857-A1 Tetrahydrocarbazole derivatives and their pharmaceutical use SMITHKLINE BEECHAM CORPORATION 2006-07-06 US claimed
US-12521397-B2 Nucleotide analogs THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2026-01-13 US disclosed
EP-4581025-A1 PYRIDAZINON DERIVATIVES AS KAT2 DEGRADERS FOR THE TREATMENT OF PROLIFERATIVE DISORDERS Auron Therapeutics, Inc. (US) 2025-07-09 EP disclosed
US-12350274-B2 Nucleotide analogs THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2025-07-08 US disclosed
WO-2024220843-A1 TECHNOLOGIES TARGETING CELL STATES AURON THERAPEUTICS, INC. (US) 2024-10-24 WO disclosed
US-20240325373-A1 METHODS AND COMPOSITIONS FOR INHIBITION OF DIHYDROOROTATE DEHYDROGENASE IN COMBINATION WITH AN ANTI-CD47-SIRPA THERAPEUTIC AGENT OHIO STATE INNOVATION FOUNDATION (US) 2024-10-03 US disclosed
US-20240245664-A1 METHODS OF USING USP15 INHIBITORS THE CURATORS OF THE UNIVERSITY OF MISSOURI 2024-07-25 US disclosed
US-20090170906-A1 HCV INHIBITORS SMITHKLINE BEECHAM CORPORATION 2009-07-02 US disclosed
US-7419997-B2 Tetrahydrocarbazole derivatives and their pharmaceutical use SMITHKLINE BEECHAM CORPORATION (US) 2008-09-02 US disclosed
US-7419997-B2 Tetrahydrocarbazole derivatives and their pharmaceutical use SMITHKLINE BEECHAM CORPORATION (US) 2008-09-02 US disclosed
US-7419997-B2 Tetrahydrocarbazole derivatives and their pharmaceutical use SMITHKLINE BEECHAM CORPORATION (US) 2008-09-02 US disclosed
US-20060148857-A1 Tetrahydrocarbazole derivatives and their pharmaceutical use SMITHKLINE BEECHAM CORPORATION 2006-07-06 US disclosed
EP-1646610-A1 TETRAHYDROCARBAZOLE DERIVATIVES AND THEIR PHARMACEUTICAL USE SmithKline Beecham Corporation (US) 2006-04-19 EP disclosed
WO-2005005386-A1 TETRAHYDROCARBAZOLE DERIVATIVES AND THEIR PHARMACEUTICAL USE SMITHKLINE BEECHAM CORPORATION (US) 2005-01-20 WO 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 (5 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-20090170906-A1 HCV INHIBITORS HAVCR2, MAVS, EIF2AK2 DHODH 103/4885ALOX15 1407/4885SMN1; SMN2 4443/4885
US-20240325373-A1 METHODS AND COMPOSITIONS FOR INHIBITION OF DIHYDROOROTATE DEHYDROGENASE IN COMBINATION WITH AN ANTI-CD47-SIRPA THERAPEUTIC AGENT DHODH, CD47, IDH1 DHODH 1/4885ALOX15 2778/4885SMN1; SMN2 3497/4885
US-12350274-B2 Nucleotide analogs NUDT1, DUT, DPYD DHODH 178/4885ALOX15 3316/4885SMN1; SMN2 3595/4885
US-20220280513-A1 ENHANCING THE ANTIVIRAL EFFICACY OF RNA VIRUS INHIBITION BY COMBINATION WITH MODULATORS OF PYRIMIDINE METABOLISM EIF2AK2, RNGTT, RNMT DHODH 167/4885ALOX15 2468/4885SMN1; SMN2 1371/4885
US-20060148857-A1 Tetrahydrocarbazole derivatives and their pharmaceutical use HMBS, UGT2B17, TPMT DHODH 62/4885ALOX15 939/4885SMN1; SMN2 4735/4885

“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.