SCHEMBL476875

SCHEMBL476875

Clc1cccc2c1ccc1ccccc12

nearest known ligand 0.73

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP2A6 P11509 5/20 0.73
CYP1A2 P05177 5/20 0.73
HPRT1 P00492 3/20 0.67
ALDH1A1 P00352 3/20 0.57
HSD17B10 Q99714 3/20 0.57
TDP1 Q9NUW8 2/20 0.57
TSHR P16473 1/20 0.57
PAX8 Q06710 1/20 0.54
MAPT P10636 2/20 0.53
LMNA P02545 1/20 0.53
CYP3A4 P08684 1/20 0.53
APEX1 P27695 1/20 0.53
MAPK1 P28482 1/20 0.53
PMP22 Q01453 1/20 0.53
NR4A2 P43354 1/20 0.48
HIF1A Q16665 1/20 0.48
CYP1B1 Q16678 1/20 0.48
THRB P10828 1/20 0.48
HPGD P15428 1/20 0.48
L3MBTL1 Q9Y468 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
SCHEMBL3710185 1.00 CYP2A6 (0.73) CYP2A6CYP1A2HPRT1ALDH1A1HSD17B10
Hydrochloric Acid SCHEMBL8112381 0.98 CYP2A6 (0.70) CYP2A6CYP1A2HPRT1ALDH1A1HSD17B10
Fluoride SCHEMBL28034452 0.96 CYP2A6 (0.67) CYP2A6CYP1A2HPRT1ALDH1A1HSD17B10
Phenanthrene SCHEMBL9753553 0.90 CYP2A6 (0.90) CYP2A6CYP1A2HPRT1ALDH1A1HSD17B10
SCHEMBL29351228 0.85 CYP2A6 (1.00) CYP2A6CYP1A2HPRT1ALDH1A1HSD17B10
SCHEMBL27987885 0.85 CYP2A6 (1.00) CYP2A6CYP1A2HPRT1ALDH1A1HSD17B10
SCHEMBL31310956 0.85 CYP2A6 (1.00) CYP2A6CYP1A2HPRT1ALDH1A1HSD17B10
SCHEMBL19854 0.85 CYP2A6 (1.00) CYP2A6CYP1A2HPRT1ALDH1A1HSD17B10
SCHEMBL30887598 0.85 CYP1A2 (0.64) CYP2A6CYP1A2HPRT1ALDH1A1HSD17B10
SCHEMBL22211948 0.85 CYP1A2 (0.64) CYP2A6CYP1A2HPRT1ALDH1A1HSD17B10

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119633844-A Selective hydrogenation dechlorination catalyst for chlorinated organic compounds and preparation method thereof 江苏扬农化工集团有限公司 2025-03-18 CN claimed
US-5369214-A Method for selective dehalogenation of halogenated polyaromatic compounds THE UNITED STATES OF AMERICA AS REPRESENTED BY THE UNITED STATES DEPARTMENT OF ENERGY (US) 1994-11-29 US claimed
CN-119633844-A Selective hydrogenation dechlorination catalyst for chlorinated organic compounds and preparation method thereof 江苏扬农化工集团有限公司 2025-03-18 CN disclosed
US-20250019563-A1 COMPOSITION INCLUDING ADDITION CONDENSATION PRODUCT OF AROMATIC COMPOUND AND CARBONYL COMPOUND AND THIOL COMPOUND, METHOD FOR PRODUCING COMPOSITION, SCALE ADHESION PREVENTION AGENT, REACTION APPARATUS, POLYMER, AND METHOD FOR PRODUCING POLYMER SHIN-ETSU CHEMICAL CO., LTD. (JP) 2025-01-16 US disclosed
CN-118930586-A Near infrared light excited iridium (III) complex photosensitizer, preparation method and application 华东交通大学 2024-11-12 CN disclosed
CN-118759067-A Method for detecting monochlorotricyclic aromatic compounds and application thereof 广州市食品检验所(广州市酒类检测中心) 2024-10-11 CN disclosed
CN-116924870-A Synthesis method of 1-substituted phenanthrene compound 西北师范大学 2023-10-24 CN disclosed
US-20230241244-A1 NANO-ENABLED IMMUNOTHERAPY IN CANCER THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2023-08-03 US disclosed
EP-3018118-B1 BASE GENERATOR, BASE-REACTIVE COMPOSITION CONTAINING SAID BASE GENERATOR, AND BASE GENERATION METHOD FUJIFILM WAKO PURE CHEMICAL CORP (JP) 2023-07-05 EP disclosed
CN-116116205-A Method for retarding generation of chloro-and bromo-polycyclic aromatic hydrocarbon by polycyclic aromatic hydrocarbon precursor 国科大杭州高等研究院 2023-05-16 CN disclosed
US-20230037858-A1 COMPOSITION CONTAINING ADDITION CONDENSATION PRODUCT, METHOD FOR PRODUCING SAME, USE OF SAME, POLYMERIZATION VESSEL, AND METHOD FOR PRODUCING POLYMER SHIN-ETSU CHEMICAL CO., LTD. (JP) 2023-02-09 US disclosed
US-5369214-A Method for selective dehalogenation of halogenated polyaromatic compounds THE UNITED STATES OF AMERICA AS REPRESENTED BY THE UNITED STATES DEPARTMENT OF ENERGY (US) 1994-11-29 US disclosed
CN-1006386-B PROCESS FOR PRODUCTION OF VINYL CHLORIDE POLYMER SHINETSU CHEM IND CO (JP) 1990-01-10 CN disclosed
EP-0172427-B1 PROCESS FOR PRODUCTION OF VINYL CHLORIDE POLYMER Shin-Etsu Chemical Co., Ltd. (JP) 1989-07-05 EP disclosed
US-4814489-A ALKYLATION MONSANTO COMPANY (US) 1989-03-21 US disclosed
US-4758639-A Process for production of vinyl polymer SHIN-ETSU CHEMICAL CO., LTD. (JP) 1988-07-19 US disclosed
US-4757124-A Suspension or emulsion polymerizing vinyl chloride monomer or mixture of vinyl chloride with vinyl monomer copolymerizable therewith in reactor with walls coated with antiscaling compound containing dye or pigments SHIN-ETSU CHEMICAL CO., LTD. (JP) 1988-07-12 US disclosed
CN-85107531-A Process for producing vinyl chloride polymer 1987-01-21 CN disclosed
EP-0172427-A2 Process for production of vinyl chloride polymer Shin-Etsu Chemical Co., Ltd. (JP) 1986-02-26 EP disclosed
US-4152504-A HIGH MOLECULAR WEIGHT, ALKENYLSODIUM-SODIUM ALKOXIDE CATALYSTS DENKI KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1979-05-01 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-20230241244-A1 NANO-ENABLED IMMUNOTHERAPY IN CANCER IDO1, IDO2, BID CYP2A6 873/4885CYP1A2 505/4885HPRT1 1766/4885

“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.