SCHEMBL6259352

SCHEMBL6259352

O=[N+]([O-])c1ccccc1CCCO

nearest known ligand 0.63

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 7/20 0.63
TSHR P16473 1/20 0.63
HPGD P15428 1/20 0.53
CA12 O43570 1/20 0.48
SIGMAR1 Q99720 1/20 0.48
L3MBTL1 Q9Y468 1/20 0.47
TDP1 Q9NUW8 1/20 0.46
RAB9A P51151 3/20 0.45
SMN1; SMN2 Q16637 3/20 0.45
NPC1 O15118 2/20 0.45
MEN1 O00255 2/20 0.45
KMT2A Q03164 2/20 0.45
CYP3A4 P08684 1/20 0.45
CYP2D6 P10635 1/20 0.45
CYP2C19 P33261 1/20 0.45
GPR35 Q9HC97 1/20 0.45
HTT P42858 1/20 0.45
KDM4E B2RXH2 1/20 0.44

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
SCHEMBL7564163 0.94 ALDH1A1 (0.61) ALDH1A1TSHRHPGDCA12SIGMAR1
SCHEMBL8576604 0.93 ALDH1A1 (0.59) ALDH1A1TSHRHPGDCA12SIGMAR1
SCHEMBL249846 0.88 ALDH1A1 (0.68) ALDH1A1TSHRHPGDCA12SIGMAR1
Nitric Acid SCHEMBL9873962 0.85 ALDH1A1 (0.63) ALDH1A1TSHRHPGDCA12SIGMAR1
SCHEMBL9820308 0.84 ALDH1A1 (0.46) ALDH1A1TSHRHPGDCA12SIGMAR1
SCHEMBL3202573 0.83 ALDH1A1 (0.72) ALDH1A1TSHRHPGDSIGMAR1L3MBTL1
SCHEMBL8867793 0.82 ALDH1A1 (0.60) ALDH1A1TSHRHPGDSIGMAR1L3MBTL1
SCHEMBL68381 0.82 ALDH1A1 (0.70) ALDH1A1TSHRHPGDCA12L3MBTL1
SCHEMBL29699944 0.82 ALDH1A1 (0.70) ALDH1A1TSHRHPGDCA12L3MBTL1
SCHEMBL6889642 0.81 ALDH1A1 (0.54) ALDH1A1TSHRHPGDCA12SIGMAR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-100357256-C Method for synthesizing o-aminophenylpropyl alcohol UNIV SHANGHAI (CN) 2007-12-26 CN claimed
CN-1760173-A Method for synthesizing o-aminophenylpropyl alcohol UNIV SHANGHAI (CN) 2006-04-19 CN claimed
EP-3958865-B1 4H-PYRROLO[3,2-C]PYRIDIN-4-ONE DERIVATIVES BAYER AG (DE) 2025-12-10 EP disclosed
US-12403135-B2 4H-pyrrolo[3,2-c]pyridin-4-one derivatives BAYER AKTIENGESELLSCHAFT (DE) 2025-09-02 US disclosed
US-20230257380-A1 TROPOMYOSIN RECEPTOR KINASE (TRK) DEGRADATION COMPOUNDS AND METHODS OF USE CULLGEN (SHANGHAI), INC. (CN) 2023-08-17 US disclosed
EP-3700904-B1 4H-PYRROLO[3,2-C]PYRIDIN-4-ONE DERIVATIVES BAYER AG (DE) 2023-07-19 EP disclosed
US-20220378762-A1 4H-PYRROLO[3,2-C]PYRIDIN-4-ONE DERIVATIVES BAYER AKTIENGESELLSCHAFT (DE) 2022-12-01 US disclosed
US-11339157-B1 4H-pyrrolo[3,2-c]pyridin-4-one derivatives BAYER AKTIENGESELLSCHAFT (DE) 2022-05-24 US disclosed
EP-3958865-A1 4H-PYRROLO[3,2-C]PYRIDIN-4-ONE DERIVATIVES Bayer Aktiengesellschaft (DE) 2022-03-02 EP disclosed
WO-2020216774-A1 4H-PYRROLO[3,2-C]PYRIDIN-4-ONE DERIVATIVES BAYER AKTIENGESELLSCHAFT (DE) 2020-10-29 WO disclosed
EP-3700904-A1 4H-PYRROLO[3,2-C]PYRIDIN-4-ONE DERIVATIVES Bayer AG (DE) 2020-09-02 EP disclosed
US-8658572-B2 Whole proteome tiling microarrays ROCHE NIMBLEGEN, INC. (US) 2014-02-25 US disclosed
WO-2013140419-A1 A PROCESS FOR SYNTHESIS OF CHIRAL 3-SUBSTITUTED TETRAHYDROQUINOLINE DERIVATIVES COUNCIL OF SCIENTIFIC & INDUSTRIAL RESEARCH (IN) 2013-09-26 WO disclosed
US-20120245057-A1 WHOLE PROTEOME TILING MICROARRAYS Roche Sequencing Solutions, Inc. 2012-09-27 US disclosed
US-20120238477-A1 METHODS FOR SYNTHESIS OF AN OLIGOPEPTIDE MICROARRAY Roche Sequencing Solutions, Inc. 2012-09-20 US disclosed
CN-100357256-C Method for synthesizing o-aminophenylpropyl alcohol UNIV SHANGHAI (CN) 2007-12-26 CN disclosed
CN-1760173-A Method for synthesizing o-aminophenylpropyl alcohol UNIV SHANGHAI (CN) 2006-04-19 CN disclosed
WO-2005073389-A1 METHOD FOR PRODUCING β-HYDROXY NITRO COMPOUNDS MADE FROM ALDEHYDES AND NITROALKANES WHILE USING A HYDROXY NITRILE LYASE ANGEWANDTE BIOKATALYSE-KOMPETENZZENTRUM GMBH (AT) 2005-08-11 WO disclosed
WO-2003026664-A1 2-PHENYLAMINO-4- (5-PYRAZOLYLAMINO) -PYRAMIDINE DERIVATIVES AS KINASE INHIBITORS, IN PARTICULAR, SRC KINASE INHIBITORS BAYER CORPORATION (US) 2003-04-03 WO disclosed
US-5686484-A ANTHELMINTICS, ACARICIDES, INSECTICIDES SANKYO CO., LTD. (JP) 1997-11-11 US 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-20230257380-A1 TROPOMYOSIN RECEPTOR KINASE (TRK) DEGRADATION COMPOUNDS AND METHODS OF USE MUSK, ERBB2, NTRK1 ALDH1A1 4113/4885TSHR 652/4885HPGD 3378/4885
US-20220378762-A1 4H-PYRROLO[3,2-C]PYRIDIN-4-ONE DERIVATIVES EGFR, ERBB2, ERBB4 ALDH1A1 1255/4885TSHR 2270/4885HPGD 235/4885
US-12403135-B2 4H-pyrrolo[3,2-c]pyridin-4-one derivatives EGFR, ERBB2, ERBB4 ALDH1A1 1255/4885TSHR 2270/4885HPGD 235/4885
US-11339157-B1 4H-pyrrolo[3,2-c]pyridin-4-one derivatives CYP4B1, CYP2C19, CYP3A4 ALDH1A1 387/4885TSHR 1659/4885HPGD 172/4885

“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.