SCHEMBL734618

SCHEMBL734618

CCCCCCc1ccc2ccccc2c1CCCCCC

nearest known ligand 0.47

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TYR P14679 2/20 0.47
LIPG Q9Y5X9 1/20 0.46
MAPT P10636 4/20 0.46
KDM4E B2RXH2 4/20 0.46
ALDH1A1 P00352 4/20 0.46
GAA P10253 4/20 0.46
CYP3A4 P08684 2/20 0.46
HPGD P15428 2/20 0.46
USP2 O75604 1/20 0.46
GLA P06280 1/20 0.46
CASP1 P29466 1/20 0.46
CASP7 P55210 1/20 0.46
HSD17B10 Q99714 1/20 0.46
NCEH1 Q6PIU2 1/20 0.46
HTT P42858 4/20 0.45
MEN1 O00255 3/20 0.45
KMT2A Q03164 3/20 0.45
TP53 P04637 1/20 0.45
ALOX5 P09917 1/20 0.45
ALOX15 P16050 1/20 0.45

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
SCHEMBL283798 1.00 TYR (0.47) TYRLIPGMAPTKDM4EALDH1A1
SCHEMBL284720 1.00 TYR (0.47) TYRLIPGMAPTKDM4EALDH1A1
SCHEMBL734929 1.00 TYR (0.47) TYRLIPGMAPTKDM4EALDH1A1
SCHEMBL284188 1.00 TYR (0.47) TYRLIPGMAPTKDM4EALDH1A1
SCHEMBL283786 1.00 TYR (0.47) TYRLIPGMAPTKDM4EALDH1A1
SCHEMBL236078 1.00 TYR (0.47) TYRLIPGMAPTKDM4EALDH1A1
SCHEMBL284699 1.00 TYR (0.47) TYRLIPGMAPTKDM4EALDH1A1
SCHEMBL234512 1.00 TYR (0.47) TYRLIPGMAPTKDM4EALDH1A1
SCHEMBL11381159 1.00 TYR (0.47) TYRLIPGMAPTKDM4EALDH1A1
SCHEMBL232844 1.00 TYR (0.47) TYRLIPGMAPTKDM4EALDH1A1

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 18 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115407528-B Method for generating vortex rotation based on organic molecule dichromatic spherulites 清华大学 2025-01-24 CN disclosed
CN-118271147-A Method for preparing long-chain alkyl naphthalene by alkylating naphthalene and long-chain alpha-olefin 大连理工大学 2024-07-02 CN disclosed
CN-115407528-A Method for generating vortex rotation based on organic molecule dichroic spherulites 清华大学 2022-11-29 CN disclosed
CN-107710440-B Charge-transporting varnish and organic electroluminescent element 日产化学工业株式会社 2019-12-24 CN disclosed
CN-109824467-A It is a kind of to utilize the ionic liquid-catalyzed method and its application for preparing more alkylnaphthalenes 太原理工大学 2019-05-31 CN disclosed
CN-108780924-A Electrolyte containing magnesium ions 富士胶片和光纯药株式会社 2018-11-09 CN disclosed
EP-2067782-B2 HETEROACENE DERIVATIVE, TETRAHALOTERPHENYL DERIVATIVE, AND THEIR PRODUCTION METHODS TOSOH CORP (JP) 2018-06-27 EP disclosed
CN-107778213-A One kind 1,4 2 substitutes naphthalene derivatives and application 北京鼎材科技有限公司 2018-03-09 CN disclosed
EP-2067782-B1 HETEROACENE DERIVATIVE, TETRAHALOTERPHENYL DERIVATIVE, AND THEIR PRODUCTION METHODS TOSOH CORP (JP) 2014-08-13 EP disclosed
US-8138355-B2 Heteroacene derivative, tetrahaloterphenyl derivative, and processes for producing the same TOSOH CORPORATION (JP) 2012-03-20 US disclosed
US-20090261300-A1 HETEROACENE DERIVATIVE, TETRAHALOTERPHENYL DERIVATIVE, AND PROCESSES FOR PRODUCING THE SAME TOSOH CORPORATION (JP) 2009-10-22 US disclosed
EP-2067782-A1 HETEROACENE DERIVATIVE, TETRAHALOTERPHENYL DERIVATIVE, AND THEIR PRODUCTION METHODS Tosoh Corporation (JP) 2009-06-10 EP disclosed
US-5910269-A GENERATES A LARGE SHEAR STRESS AND LOW CURRENT DENSITY, EXHIBITS EXCELLENT WITHSTANDING DIELECTRIC BREAKDOWN STRENGTH, EXHIBITS EXCELLENT FLUIDITY AND REDISPERSABILITY IN THE ABSENCE OF AN ELECTRIC FIELD NIPPON SHOKUBAI CO., LTD. (JP) 1999-06-08 US disclosed
US-4251665-A USED FOR CURING AMINO RESINS KING INDUSTRIES, INC. (US) 1981-02-17 US disclosed
US-4200729-A Curing amino resins with aromatic sulfonic acid oxa-azacyclopentane adducts KING INDUSTRIES, INC (US) 1980-04-29 US disclosed
US-4128565-A Process for preparing methyltin chlorides SANKYO ORGANIC CHEMICALS COMPANY LIMITED (JP) 1978-12-05 US disclosed
US-3960688-A AMINOPLAST CROSSLINKING AGENT, POLYMER, AROMATIC SULFONIC ACID CATALYST AMERICAN CYANAMID COMPANY (US) 1976-06-01 US disclosed
US-3959399-A FROM NAPHTHALENE AND AN ALKENE, ACID CATALYST NALCO CHEMICAL COMPANY (US) 1976-05-25 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-20090261300-A1 HETEROACENE DERIVATIVE, TETRAHALOTERPHENYL DERIVATIVE, AND PROCESSES FOR PRODUCING THE SAME AS3MT, TERT, TEAD1 TYR 65/4885LIPG 4208/4885MAPT 1194/4885

“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.