SCHEMBL1576764

SCHEMBL1576764

CCCCc1ccccc1Sc1ccccc1CCCC

nearest known ligand 0.46

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
LIPG Q9Y5X9 1/20 0.46
CYP3A4 P08684 1/20 0.42
CYP2D6 P10635 1/20 0.42
CYP2C9 P11712 1/20 0.42
SLC6A4 P31645 5/20 0.42
SLC6A3 Q01959 4/20 0.42
SLC6A2 P23975 4/20 0.42
LMNA P02545 2/20 0.42
TLR8 Q9NR97 1/20 0.40
IFNAR1 P17181 1/20 0.40
ALDH1A1 P00352 1/20 0.39
NPY1R P25929 1/20 0.39
MAPK1 P28482 1/20 0.39
NPY2R P49146 1/20 0.39
TYR P14679 1/20 0.38
NR1H2 P55055 1/20 0.38
NR1H3 Q13133 1/20 0.38
CYSLTR2 Q9NS75 1/20 0.37
CYSLTR1 Q9Y271 1/20 0.37

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
SCHEMBL8227185 0.94 LIPG (0.53) LIPGSLC6A4SLC6A3SLC6A2LMNA
SCHEMBL10698150 0.92 LIPG (0.56) LIPGNR1H2NR1H3CYSLTR2CYSLTR1
SCHEMBL1800362 0.92 LIPG (0.56) LIPGNR1H2NR1H3CYSLTR2CYSLTR1
SCHEMBL786161 0.92 LIPG (0.56) LIPGNR1H2NR1H3CYSLTR2CYSLTR1
SCHEMBL5443171 0.92 LIPG (0.56) LIPGNR1H2NR1H3CYSLTR2CYSLTR1
SCHEMBL146935 0.90 LIPG (0.55) LIPGNR1H2NR1H3CYSLTR2CYSLTR1
SCHEMBL30463283 0.90 LIPG (0.55) LIPGNR1H2NR1H3CYSLTR2CYSLTR1
SCHEMBL6679998 0.90 LIPG (0.55) LIPGNR1H2NR1H3CYSLTR2CYSLTR1
SCHEMBL6404803 0.90 LIPG (0.55) LIPGNR1H2NR1H3CYSLTR2CYSLTR1
SCHEMBL29361835 0.90 LIPG (0.55) LIPGNR1H2NR1H3CYSLTR2CYSLTR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2481760-B1 INITIATOR SYSTEM FOR CATIONIC POLYMERIZATION AND POLYMERIZATION METHOD USING SAME CHINA PETROLEUM & CHEM CORP (CN) 2021-05-05 EP claimed
CN-122006631-A Device for preparing hydrogen fluoride by molecular recognition complexation method and application thereof 浙江大学衢州研究院 2026-05-12 CN disclosed
EP-3527593-B1 ISOCYANATE COMPOSITION, METHOD FOR PRODUCING ISOCYANATE COMPOSITION, AND METHOD FOR PRODUCING ISOCYANATE POLYMER ASAHI CHEMICAL IND (JP) 2025-07-23 EP disclosed
EP-3527600-B1 ISOCYANATE COMPOSITION AND PRODUCTION METHOD FOR ISOCYANATE POLYMER ASAHI CHEMICAL IND (JP) 2025-07-09 EP disclosed
CN-112979917-B Isocyanate composition, method for producing isocyanate composition, and method for producing isocyanate polymer 旭化成株式会社 2023-04-25 CN disclosed
US-20230114799-A1 ISOCYANATE COMPOSITION AND METHOD FOR PRODUCING ISOCYANATE POLYMER ASAHI KASEI KABUSHIKI KAISHA (JP) 2023-04-13 US disclosed
US-11548975-B2 Isocyanate composition and method for producing isocyanate polymer ASAHI KASEI KABUSHIKI KAISHA (JP) 2023-01-10 US disclosed
CN-115028560-A Gem-difluoroallyl compound and preparation method thereof 昆明理工大学 2022-09-09 CN disclosed
CN-109790269-B Isocyanate composition, method for producing isocyanate composition, and method for producing isocyanate polymer 旭化成株式会社 2022-06-14 CN disclosed
CN-109803992-B Isocyanate composition and method for producing isocyanate polymer 旭化成株式会社 2022-05-24 CN disclosed
US-8883943-B2 Isoolefin polymers and process for preparing the same CHINA PETROLEUM & CHEMICAL CORPORATION (CN) 2014-11-11 US disclosed
US-20120329973-A1 INITIATING SYSTEM FOR CATIONIC POLYMERIZATION AND POLYMERIZATION PROCESS BEIJING UNIVERSITY OF CHEMICAL TECHNOLOGY (CN) 2012-12-27 US disclosed
US-20120238715-A1 ISOOLEFIN POLYMERS AND PROCESS FOR PREPARING THE SAME CHINA PETROLEUM & CHEMICAL CORPORATION (CN) 2012-09-20 US disclosed
EP-2481760-A1 INITIATOR SYSTEM FOR CATIONIC POLYMERIZATION AND POLYMERIZATION METHOD USING SAME China Petroleum & Chemical Corporation (CN) 2012-08-01 EP disclosed
EP-2481759-A1 ISO-OLEFIN POLYMER AND PREPARATION METHOD THEREOF China Petroleum & Chemical Corporation (CN) 2012-08-01 EP disclosed
WO-2011039474-A1 MEDIUM- OR HIGH-VOLTAGE ELECTRIC CABLE NEXANS (FR) 2011-04-07 WO disclosed
EP-1492753-A1 PROCESS FOR CONVERTING ALCOHOLS TO CARBONYL COMPOUNDS Ciba SC Holding AG (CH) 2005-01-05 EP disclosed
WO-2003084911-A1 PROCESS FOR CONVERTING ALCOHOLS TO CARBONYL COMPOUNDS CIBA SPECIALTY CHEMICALS HOLDING INC. (CH) 2003-10-16 WO disclosed
EP-0409412-A2 Diaryl ether cyclic ethers IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1991-01-23 EP disclosed
US-4124646-A Process for producing thioanisole SEITETSU KAGAKU CO., LTD. (JP) 1978-11-07 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-11548975-B2 Isocyanate composition and method for producing isocyanate polymer IDH3A, IDH2, IDH3B LIPG 4704/4885CYP3A4 84/4885CYP2D6 600/4885
US-20230114799-A1 ISOCYANATE COMPOSITION AND METHOD FOR PRODUCING ISOCYANATE POLYMER IDH3A, IDH2, IDH3B LIPG 4697/4885CYP3A4 165/4885CYP2D6 558/4885

“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.