SCHEMBL983097

SCHEMBL983097

CC(c1ccccc1)(c1ccccc1)c1ccccc1O

nearest known ligand 0.60

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 5/20 0.60
TDP1 Q9NUW8 2/20 0.60
TSHR P16473 1/20 0.60
ESR1 P03372 3/20 0.56
ESR2 Q92731 3/20 0.56
CYP3A4 P08684 2/20 0.45
ALOX15 P16050 3/20 0.41
HDAC4 P56524 2/20 0.39
HDAC2 Q92769 2/20 0.39
HDAC8 Q9BY41 2/20 0.39
CA2 P00918 2/20 0.39
MAPK1 P28482 1/20 0.39
MAPT P10636 2/20 0.39
HIF1A Q16665 2/20 0.39
LMNA P02545 2/20 0.39
HSD17B10 Q99714 2/20 0.39
KDM4E B2RXH2 1/20 0.39
NPC1 O15118 1/20 0.39
CA12 O43570 1/20 0.39
GMNN O75496 1/20 0.39

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
SCHEMBL29688168 0.95 ALDH1A1 (0.60) ALDH1A1TDP1TSHRESR1ESR2
SCHEMBL1410514 0.95 ALDH1A1 (0.60) ALDH1A1TDP1TSHRESR1ESR2
SCHEMBL9243349 0.92 ESR1 (0.70) ALDH1A1TDP1TSHRESR1ESR2
SCHEMBL9567886 0.87 ESR1 (0.63) ALDH1A1TDP1TSHRESR1ESR2
SCHEMBL29440405 0.85 ALDH1A1 (0.71) ALDH1A1TDP1TSHRESR1ESR2
SCHEMBL410880 0.85 ALDH1A1 (0.71) ALDH1A1TDP1TSHRESR1ESR2
SCHEMBL23861532 0.84 ALDH1A1 (0.52) ALDH1A1TDP1TSHRESR1ESR2
SCHEMBL9567870 0.83 ESR1 (0.63) ALDH1A1TDP1TSHRESR1ESR2
Bicarbonate SCHEMBL7096874 0.82 ALDH1A1 (0.60) ALDH1A1TDP1TSHRESR1ESR2
SCHEMBL11645702 0.82 ALDH1A1 (0.60) ALDH1A1TDP1TSHRESR1ESR2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118496435-B Functional polymer, preparation method and application thereof, tin powder modification method and tin paste 化学与精细化工广东省实验室 2024-10-01 CN claimed
CN-115885984-A Pyraclostrobin and epoxiconazole microemulsion as well as preparation method and application thereof 上海悦联生物科技有限公司 2023-04-04 CN claimed
US-4322312-A Process for purification of non-ionic emulsifiers BAYER AKTIENGESELLSCHAFT (DE) 1982-03-30 US claimed
CN-112394622-B Low-etching-rate developer composition and preparation method thereof 芯越微电子材料(嘉兴)有限公司 2025-05-09 CN disclosed
CN-115885984-A Pyraclostrobin and epoxiconazole microemulsion as well as preparation method and application thereof 上海悦联生物科技有限公司 2023-04-04 CN disclosed
EP-2275405-B1 PROCESS FOR PRODUCING ISOCYANATE USING DIARYL CARBONATE ASAHI CHEMICAL IND (JP) 2019-04-24 EP disclosed
CN-109535396-A The 4th subgroup metal complex of porous organic polymer ligand and purposes 吉林大学 2019-03-29 CN disclosed
EP-2275406-B1 PROCESS FOR PRODUCING ISOCYANATE ASAHI CHEMICAL IND (JP) 2018-11-28 EP disclosed
EP-2792673-B1 Carbamic acid ester derivatives for the production of isocyanate and aromatic hydroxy compounds ASAHI CHEMICAL IND (JP) 2018-07-25 EP disclosed
US-9637445-B2 Isocyanate production process using composition containing carbamic acid ester and aromatic hydroxy compound, and composition for transfer and storage of carbamic acid ester ASAHI KASEI CHEMICALS CORPORATION (JP) 2017-05-02 US disclosed
EP-2147909-B1 METHOD FOR PRODUCTION OF ISOCYANATE USING COMPOSITION COMPRISING CARBAMIC ACID ESTER AND AROMATIC HYDROXY COMPOUND, AND COMPOSITION FOR TRANSPORT OR STORAGE OF CARBAMIC ACID ESTER ASAHI CHEMICAL IND (JP) 2016-12-14 EP disclosed
US-20100274047-A1 PROCESS FOR PRODUCING OF ISOCYANATES AND AROMATIC HYDROXY COMPOUNDS ASAHI KASEI CHEMICALS CORPORATION (JP) 2010-10-28 US disclosed
EP-2213658-A1 METHOD FOR PRODUCTION OF ISOCYANATE AND AROMATIC HYDROXY COMPOUND Asahi Kasei Chemicals Corporation (JP) 2010-08-04 EP disclosed
US-20100113823-A1 ISOCYANATE PRODUCTION PROCESS USING COMPOSITION CONTAINING CARBAMIC ACID ESTER AND AROMATIC HYDROXY COMPOUND, AND COMPOSITION FOR TRANSFER AND STORAGE OF CARBAMIC ACID ESTER ASAHI KASEI CHEMICALS CORPORATION (JP) 2010-05-06 US disclosed
EP-2147909-A1 METHOD FOR PRODUCTION OF ISOCYANATE USING COMPOSITION COMPRISING CARBAMIC ACID ESTER AND AROMATIC HYDROXY COMPOUND, AND COMPOSITION FOR TRANSPORT OR STORAGE OF CARBAMIC ACID ESTER Asahi Kasei Chemicals Corporation (JP) 2010-01-27 EP disclosed
US-5932641-A BLEND WITH THERMOSETTING, THERMOPLASTIC POLYMERS COATEX S.A. (FR) 1999-08-03 US disclosed
US-4322312-A Process for purification of non-ionic emulsifiers BAYER AKTIENGESELLSCHAFT (DE) 1982-03-30 US disclosed
US-4299959-A N-SUBSTITUTED IMINOCOUMARINS CIBA-GEIGY CORPORATION (US) 1981-11-10 US disclosed
EP-0012875-A1 Non-ionic emulsifying agents and process for their purification BAYER AG (DE) 1980-07-09 EP disclosed
US-4153618-A N-SUBSTITUTED IMINOCOUMARINS CIBA-GEIGY CORPORATION (US) 1979-05-08 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 (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-20100113823-A1 ISOCYANATE PRODUCTION PROCESS USING COMPOSITION CONTAINING CARBAMIC ACID ESTER AND AROMATIC HYDROXY COMPOUND, AND COMPOSITION FOR TRANSFER AND STORAGE OF CARBAMIC ACID ESTER PAH, APEH, CPS1 ALDH1A1 2908/4885TDP1 1942/4885TSHR 4479/4885
US-20100274047-A1 PROCESS FOR PRODUCING OF ISOCYANATES AND AROMATIC HYDROXY COMPOUNDS PAH, APEH, HPD ALDH1A1 2913/4885TDP1 2806/4885TSHR 4571/4885

“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.