SCHEMBL29359161

SCHEMBL29359161

Cn1cnc2ccccc21

nearest known ligand 0.59

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
TDP1 Q9NUW8 1/20 0.59
GRM5 P41594 1/20 0.53
HTT P42858 4/20 0.52
CYP11B1 P15538 4/20 0.50
CYP11B2 P19099 4/20 0.50
LMNA P02545 3/20 0.48
SMN1; SMN2 Q16637 2/20 0.48
MEN1 O00255 1/20 0.48
HPGD P15428 1/20 0.48
KMT2A Q03164 1/20 0.48
HSD17B10 Q99714 1/20 0.48
PKM P14618 1/20 0.47
POLB P06746 1/20 0.47
TNF P01375 1/20 0.47
EGLN3 Q9H6Z9 1/20 0.46
L3MBTL1 Q9Y468 1/20 0.46

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
SCHEMBL5399 1.00 TDP1 (0.59) TDP1GRM5HTTCYP11B1CYP11B2
SCHEMBL28652434 0.98 TDP1 (0.57) TDP1GRM5HTTCYP11B1CYP11B2
Bromide SCHEMBL10432264 0.98 TDP1 (0.57) TDP1GRM5HTTCYP11B1CYP11B2
Bromide SCHEMBL6955674 0.98 TDP1 (0.57) TDP1GRM5HTTCYP11B1CYP11B2
Hydrochloric Acid SCHEMBL7206595 0.98 TDP1 (0.57) TDP1GRM5HTTCYP11B1CYP11B2
Hydrochloric Acid SCHEMBL3713895 0.98 TDP1 (0.57) TDP1GRM5HTTCYP11B1CYP11B2
Iodide SCHEMBL15375366 0.98 TDP1 (0.57) TDP1GRM5HTTCYP11B1CYP11B2
Methylamine SCHEMBL28557648 0.96 TDP1 (0.55) TDP1GRM5HTTCYP11B1CYP11B2
SCHEMBL30395666 0.92 TDP1 (0.52) TDP1GRM5HTTCYP11B1CYP11B2
SCHEMBL15639423 0.92 TDP1 (0.52) TDP1GRM5HTTCYP11B1CYP11B2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12545682-B2 Heterocyclic derivatives as P2X7 receptor antagonists BREYE THERAPEUTICS APS (DK) 2026-02-10 US claimed
EP-4655285-A1 CALIX[4]ARENES WITH HIGH ANTICANCER ACTIVITY Université Grenoble Alpes (FR) 2025-12-03 EP claimed
WO-2025149628-A1 PIPERIDINE DERIVATIVES AS INHIBITORS OF NICOTINAMIDE N-METHYL TRANSFERASE ASTRAZENECA AB (SE) 2025-07-17 WO claimed
CN-119978002-A Mononuclear zinc complex and preparation method and application thereof 广西师范大学 2025-05-13 CN claimed
WO-2025049402-A1 KRAS MODULATORS AND USES THEREOF QUANTA THERAPEUTICS, INC. (US) 2025-03-06 WO claimed
US-20250051319-A1 COMPOUNDS AND USE THEREOF AS HDAC6 INHIBITORS AUGUSTINE THERAPEUTICS (BE) 2025-02-13 US claimed
EP-4441275-A1 METHOD FOR THE ELECTRO-OXIDATION OF A FURAN COMPOUND IFP Energies nouvelles (FR) 2024-10-09 EP claimed
WO-2024156819-A1 CALIX[4]ARENES WITH HIGH ANTICANCER ACTIVITY UNIVERSITE GRENOBLE ALPES (FR) 2024-08-02 WO claimed
CN-116217491-B Benzimidazole single-functionalized column [5] arene N-heterocyclic carbene catalyst and preparation method and application thereof 青岛科技大学 2024-05-14 CN claimed
CN-112955992-B Dye sensitized photovoltaic cell 环境光子学公司 2024-04-02 CN claimed
US-20240034737-A1 Heterocyclic Derivatives as P2X7 Receptor Antagonists BREYE THERAPEUTICS APS (DK) 2024-02-01 US claimed
CN-117430738-A Catalyst component for olefin polymerization, catalyst and application thereof 中国石油化工股份有限公司 2024-01-23 CN claimed
WO-2023099689-A1 METHOD FOR THE ELECTRO-OXIDATION OF A FURAN COMPOUND IFP Energies Nouvelles (FR) 2023-06-08 WO claimed
CN-116075510-A 1H-benzo [ d ] imidazole derivatives as TLR9 inhibitors for the treatment of fibrosis 百时美施贵宝公司 2023-05-05 CN claimed
CN-116507617-B 1- (2- (4-Cyclopropyl-1H-1, 2, 3-triazol-1-yl) acetyl) -4-hydroxypyrrolidine-2-carboxamide derivatives as VHL inhibitors 基因泰克公司 2026-05-22 CN disclosed
CN-122029158-A EGFR inhibitors 缆图药品公司 2026-05-12 CN disclosed
US-20260115201-A1 POTENTIAL THERAPEUTICS FOR FIBROSIS BY BLOCKING THE INCREASE OF A KEY ENZYME TEXAS A & M UNIV SYS (US) 2026-04-30 US disclosed
WO-2022035917-A1 SYNTHESIS OF FLUORINATED NUCLEOTIDES MERCK SHARP & DOHME CORP. (US) 2022-02-17 WO disclosed
US-11241398-B2 Affinity medicant conjugate AF CHEMICALS, LLC (US) 2022-02-08 US disclosed
EP-3941462-A1 PHARMACEUTICAL COMPOUNDS FOR THE TREATMENT OF COMPLEMENT MEDIATED DISORDERS Achillion Pharmaceuticals, Inc. (US) 2022-01-26 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 (4 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-20250051319-A1 COMPOUNDS AND USE THEREOF AS HDAC6 INHIBITORS HDAC6, HDAC9, HDAC1 TDP1 1011/4885GRM5 1996/4885HTT 66/4885
US-20260115201-A1 POTENTIAL THERAPEUTICS FOR FIBROSIS BY BLOCKING THE INCREASE OF A KEY ENZYME DDX3X, DDX39B, DDX1 TDP1 1399/4885GRM5 4766/4885HTT 3518/4885
US-20240034737-A1 Heterocyclic Derivatives as P2X7 Receptor Antagonists P2RX7, P2RX3, P2RX1 TDP1 1868/4885GRM5 328/4885HTT 1934/4885
US-12545682-B2 Heterocyclic derivatives as P2X7 receptor antagonists P2RX7, P2RX3, P2RX1 TDP1 2215/4885GRM5 308/4885HTT 3447/4885

“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.