SCHEMBL1724302

SCHEMBL1724302

c1ccc(CN2CC3CCCNC3C2)cc1

nearest known ligand 0.54

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
▸ FUCA1 P04066 2/20 0.45
▸ CYP1A2 P05177 1/20 0.44
▸ CYP3A4 P08684 1/20 0.44
▸ CYP2D6 P10635 1/20 0.44
▸ CYP2C19 P33261 1/20 0.44
▸ ALDH1A1 P00352 1/20 0.44
▸ SIGMAR1 Q99720 2/20 0.44
▸ DRD2 P14416 2/20 0.43
▸ DRD3 P35462 2/20 0.43
▸ ACHE P22303 2/20 0.42
▸ BCHE P06276 1/20 0.42
▸ BACE1 P56817 1/20 0.42
▸ OPRL1 P41146 1/20 0.42

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
SCHEMBL697958 1.00 FUCA1 (0.45) FUCA1CYP1A2CYP3A4CYP2D6CYP2C19
SCHEMBL13992425 1.00 FUCA1 (0.45) FUCA1CYP1A2CYP3A4CYP2D6CYP2C19
SCHEMBL4303371 1.00 FUCA1 (0.45) FUCA1CYP1A2CYP3A4CYP2D6CYP2C19
SCHEMBL1983745 1.00 FUCA1 (0.45) FUCA1CYP1A2CYP3A4CYP2D6CYP2C19
SCHEMBL4304653 1.00 FUCA1 (0.45) FUCA1CYP1A2CYP3A4CYP2D6CYP2C19
Hydrochloric Acid SCHEMBL2339005 0.98 FUCA1 (0.44) FUCA1CYP1A2CYP3A4CYP2D6CYP2C19
Hydrochloric Acid SCHEMBL2348540 0.98 FUCA1 (0.44) FUCA1CYP1A2CYP3A4CYP2D6CYP2C19
Hydrochloric Acid SCHEMBL2542931 0.98 FUCA1 (0.44) FUCA1CYP1A2CYP3A4CYP2D6CYP2C19
SCHEMBL17228289 0.95 POLB (0.46) FUCA1CYP1A2CYP3A4CYP2D6CYP2C19
Isopropyl Alcohol SCHEMBL29020804 0.92 GRIN2B (0.44) FUCA1ALDH1A1ACHEBCHE

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119823125-A Preparation method of moxifloxacin side chain key intermediate 新天地医药技术研究院(郑州)有限公司 2025-04-15 — — CN claimed
CN-115073452-A Method for continuously synthesizing moxifloxacin side chain intermediate through heterogeneous hydrogenation in microreactor 河南新天地药业股份有限公司 2022-09-20 — — CN claimed
CN-106478487-B Pyrrolidines and its synthetic method 上海交通大学 2019-01-25 — — CN claimed
WO-2014097272-A2 METHOD FOR PRODUCTION OF (S,S)-6-BENZYLOCTAHYDRO-1H-PYRROLO[3,4-B]PYRIDINE, AN INTERMEDIATE OF AZABICYCLO PYRIDINE DERIVATIVES MANKIND RESEARCH CENTRE (IN) 2014-06-26 — — WO claimed
CN-103588772-A Preparation method of moxifloxacin intermediate UNIV SICHUAN 2014-02-19 — — CN claimed
CN-103275078-A Method for industrial production of moxifloxacin side chain SUZHOU MICRODIAG BIOLOG CO LTD 2013-09-04 — — CN claimed
WO-2012131629-A1 A PROCESS FOR PREPARATION OF INTERMEDIATE OF MOXIFLOXACIN PIRAMAL HEALTHCARE LIMITED (IN) 2012-10-04 — — WO claimed
WO-2009125425-A2 IMPROVED PROCESS FOR THE PREPARATION OF (S.S)-2.8-DIAZABICYCLO[4.3.0]NONANE NEULAND LABORATORIES LTD (IN) 2009-10-15 — — WO claimed
EP-1077979-B1 METHOD FOR PRODUCING (S,S)-BENZYL-2,8-DIAZABICYCLO 4.3.0]NONANE BAYER HEALTHCARE AG (DE) 2005-07-06 — — EP claimed
EP-1184358-A2 Process for treatment and purification of the reaction products obtained by reduction with lithium aluminium hydride BAYER AG (DE) 2002-03-06 — — EP claimed
US-20020016462-A1 Process for preparing basic organic nitrogen-containing compounds by reduction with lithium aluminum hydride BAYER AKTIENGESELLSCHAFT (DE) 2002-02-07 — — US claimed
US-6235908-B1 PREPARATION OF TARTRATE BAYER AKTIENGESELLSCHAFT (DE) 2001-05-22 — — US claimed
EP-1077979-A1 METHOD FOR PRODUCING (S,S)-BENZYL-2,8-DIAZABICYCLO 4.3.0]NONANE BAYER AG (DE) 2001-02-28 — — EP claimed
WO-1999058532-A1 METHOD FOR PRODUCING (S,S)-BENZYL-2,8-DIAZABICYCLO[4.3.0]NONANE BAYER AKTIENGESELLSCHAFT (DE) 1999-11-18 — — WO claimed
EP-4724435-A1 BIFUNCTIONAL AZINES CONJOGATES AS SELECTIVE DEGRADERS OF SMARCA2 AND THERAPEUTIC USES THEREOF Nurix Therapeutics, Inc. (US) 2026-04-15 — — EP disclosed
CN-119823125-A Preparation method of moxifloxacin side chain key intermediate 新天地医药技术研究院(郑州)有限公司 2025-04-15 — — CN disclosed
US-20250051344-A1 BIFUNCTIONAL SELECTIVE DEGRADERS OF SMARCA2 AND THERAPEUTIC USES THEREOF NURIX THERAPEUTICS, INC. 2025-02-13 — — US disclosed
US-4990517-A 7-(1-pyrrolidinyl)-3-quinolone- and -naphthyridonecarboxylic acid derivatives as antibacterial agents and feed additives BAYER AKTIENGESELLSCHAFT (DE) 1991-02-05 — — US disclosed
CN-1039589-A 7- (1-pyrrolidinyl) -3-quinolone-and 1, 5-naphthyridonecarboxylic acid derivatives and process for preparing same BAYER AG (DE) 1990-02-14 — — CN disclosed
EP-0350733-A2 7-(1-Pyrrolidinyl)-3-quinolone- and -naphthyridone-carboxylic-acid derivatives, method for their preparation and for substituted mono- and bi-cyclic pyrrolidine intermediates, and their antibacterial and feed additive compositions BAYER AG (DE) 1990-01-17 — — 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 (2 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-20020016462-A1 Process for preparing basic organic nitrogen-containing compounds by reduction with lithium aluminum hydride NIT2, NCL, ALKBH1 FUCA1 4574/4885CYP1A2 1585/4885CYP3A4 2010/4885
US-20250051344-A1 BIFUNCTIONAL SELECTIVE DEGRADERS OF SMARCA2 AND THERAPEUTIC USES THEREOF SMARCA2, SMARCE1, SMARCB1 FUCA1 3661/4885CYP1A2 3352/4885CYP3A4 4516/4885

“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.

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