SCHEMBL3785330

SCHEMBL3785330

Cc1c(Cl)cccc1C(Cl)(Cl)Cl

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 2/20 0.50
LMNA P02545 4/20 0.40
KCNN4 O15554 1/20 0.40
TSHR P16473 3/20 0.39
CYP3A4 P08684 3/20 0.39
MAPK1 P28482 1/20 0.39
TDP1 Q9NUW8 1/20 0.39
CYP1A2 P05177 2/20 0.38
CYP2A6 P11509 1/20 0.38
MAPT P10636 2/20 0.37
RAPGEF4 Q8WZA2 1/20 0.37
POLB P06746 2/20 0.36
IDO1 P14902 1/20 0.36
PIK3CA P42336 1/20 0.36
NISCH Q9Y2I1 1/20 0.35
RECQL P46063 1/20 0.34
MEN1 O00255 1/20 0.34
USP2 O75604 1/20 0.34
MT-CO2 P00403 1/20 0.34
TTR P02766 1/20 0.34

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
SCHEMBL11966007 0.83 ALDH1A1 (0.48) ALDH1A1LMNAKCNN4TSHRCYP3A4
SCHEMBL11950652 0.81 ALDH1A1 (0.46) ALDH1A1LMNAKCNN4MAPTMEN1
SCHEMBL30018318 0.79 ALDH1A1 (0.45) ALDH1A1LMNAKCNN4CYP3A4CYP1A2
SCHEMBL9442662 0.79 ALDH1A1 (0.45) ALDH1A1LMNAKCNN4CYP3A4CYP1A2
SCHEMBL16579368 0.79 ALDH1A1 (0.50) ALDH1A1LMNAKCNN4TSHRCYP3A4
SCHEMBL112040 0.78
Hydrochloric Acid SCHEMBL10426264 0.75 ALDH1A1 (0.62) ALDH1A1LMNATSHRCYP3A4TDP1
Ammonia Solution, Strong SCHEMBL1640555 0.75 ALDH1A1 (0.62) ALDH1A1LMNATSHRCYP3A4TDP1
Fluoride SCHEMBL28877073 0.75 ALDH1A1 (0.62) ALDH1A1LMNATSHRCYP3A4TDP1
SCHEMBL20847883 0.74 ALDH1A1 (0.41) ALDH1A1LMNAKCNN4MAPTRAPGEF4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119350140-A Production process of phthalic dicarboxaldehyde 酒泉亚佳化学有限公司 2025-01-24 CN claimed
CN-116675595-A Preparation process of phthalic dicarboxaldehyde 江西邦浦医药化工有限公司 2023-09-01 CN claimed
CN-213315010-U Reaction kettle for preparing tetrachloro-o-xylene 西安思科赛实业有限公司 2021-06-01 CN claimed
CN-223782780-U Adjustable power light source generator device for producing tetrachloro ortho-xylene 湖北相和精密化学有限公司 2026-01-09 CN disclosed
CN-223779939-U High-precision metering automatic filling machine device for producing tetrachloro ortho-xylene 湖北相和精密化学有限公司 2026-01-09 CN disclosed
CN-119350140-A Production process of phthalic dicarboxaldehyde 酒泉亚佳化学有限公司 2025-01-24 CN disclosed
CN-116675595-A Preparation process of phthalic dicarboxaldehyde 江西邦浦医药化工有限公司 2023-09-01 CN disclosed
CN-213315010-U Reaction kettle for preparing tetrachloro-o-xylene 西安思科赛实业有限公司 2021-06-01 CN disclosed
CN-213315010-U Reaction kettle for preparing tetrachloro-o-xylene 西安思科赛实业有限公司 2021-06-01 CN disclosed
CN-213335659-U Reation kettle temperature control device of tetrachloro o-diphenyl preparation 西安思科赛实业有限公司 2021-06-01 CN disclosed
CN-213315011-U Tetrachloro o-diphenyl preparation leads to chlorine cauldron 西安思科赛实业有限公司 2021-06-01 CN disclosed
US-20160152533-A1 METHOD FOR THE PREPARATION OF TRICHLOROMETHYL-GROUP-SUBSTITUTED BENZENE Shanghai Fanglun New Marerial Technology Co., Ltd. (CN) 2016-06-02 US disclosed
US-7858381-B2 Process for preparing high-purity, halogen-free o-phthaladehyde DSM FINE CHEMICALS AUSTRIA NFG GMBH & CO KG (AT) 2010-12-28 US disclosed
EP-1741695-B1 Process for producing high purity, halogen-free o-phthalaldehyde DSM FINE CHEM AUSTRIA GMBH (AT) 2009-07-15 EP disclosed
EP-1741695-A1 Process for producing high purity, halogen-free o-phthalaldehyde DSM Fine Chemicals Austria Nfg GmbH & Co KG (AT) 2007-01-10 EP disclosed
US-20060293542-A1 Process for preparing high-purity, halogen-free o-phthaladehyde DSM FINE CHEMICALS AUSTRIA NFG GMBH & COKG (AT) 2006-12-28 US disclosed
US-4141912-A Process for the preparation of polyhalobenzylic disulfooxonium compounds HOOKER CHEMICALS & PLASTICS CORP. (US) 1979-02-27 US disclosed
US-4075238-A Polyhalobenzylic disulfooxonium compounds HOOKER CHEMICALS & PLASTICS CORPORATION (US) 1978-02-21 US disclosed
US-4056454-A FROM O-XYLENE AND CHLORINE, CARBON TETRACHLORIDE SOLVENT DYNAMIT NOBEL AKTIENGESELLSCHAFT (DT) 1977-11-01 US disclosed
US-3981936-A Method for the preparation of bis-(bromomethyl)-tetrachlorobenzenes and their use as flame-proofing agents DYNAMIT NOBEL AKTIENGESELLSCHAFT (DT) 1976-09-21 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 (1 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-20060293542-A1 Process for preparing high-purity, halogen-free o-phthaladehyde ADH1A, ADH1C, HPD ALDH1A1 43/4885LMNA 2691/4885KCNN4 4251/4885

“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.