SCHEMBL18306930

SCHEMBL18306930

OC1(c2ccc(F)cc2)CCC1

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
OPRM1 P35372 2/20 0.50
OPRD1 P41143 2/20 0.50
OPRK1 P41145 2/20 0.50
OPRL1 P41146 2/20 0.50
DRD2 P14416 7/20 0.44
SLC6A3 Q01959 1/20 0.44
HSD11B1 P28845 1/20 0.43
SMN1; SMN2 Q16637 1/20 0.43
HTR1A P08908 2/20 0.42
DRD1 P21728 2/20 0.42
DRD5 P21918 2/20 0.42
SLC6A2 P23975 2/20 0.42
HTR2A P28223 2/20 0.42
SLC6A4 P31645 2/20 0.42
HTR7 P34969 2/20 0.42
HRH1 P35367 2/20 0.42
DRD3 P35462 2/20 0.42
HTR2B P41595 2/20 0.42
AR P10275 1/20 0.41
KCNH2 Q12809 1/20 0.41

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
SCHEMBL6154699 0.95 OPRM1 (0.50) OPRM1OPRD1OPRK1OPRL1DRD2
SCHEMBL26929227 0.94 OPRM1 (0.46) OPRM1OPRD1OPRK1OPRL1DRD2
SCHEMBL11648759 0.93 SLC6A3 (0.52) OPRM1OPRD1OPRK1OPRL1DRD2
SCHEMBL7824744 0.90 OPRM1 (0.53) OPRM1OPRD1OPRK1OPRL1DRD2
SCHEMBL31322237 0.82 DRD2 (0.58) OPRM1OPRD1OPRK1OPRL1DRD2
SCHEMBL615480 0.80 DRD2 (0.66) OPRM1OPRD1OPRK1OPRL1DRD2
SCHEMBL3640272 0.80 OPRM1 (0.46) OPRM1OPRD1OPRK1OPRL1DRD2
Ethoxycarbonyl Group SCHEMBL28100919 0.79 OPRM1 (0.39) OPRM1OPRD1OPRK1OPRL1DRD2
SCHEMBL613615 0.79 OPRM1 (0.45) OPRM1OPRD1OPRK1OPRL1DRD2
Hydrochloric Acid SCHEMBL1765160 0.79 DRD2 (0.63) OPRM1OPRD1OPRK1OPRL1DRD2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122071411-A Method for forming ester by oxidizing and breaking carbon-carbon bond by tertiary alcohol 中国科学院大连化学物理研究所 2026-05-22 CN disclosed
CN-113636977-B Synthesis method of 2-aryl benzazepine and derivatives thereof 温州大学 2022-12-20 CN disclosed
CN-112110801-B Synthetic method of gamma-aryl substituted ketone compound 浙江工业大学 2022-07-19 CN disclosed
CN-110218227-B Method for preparing aryl ketone derivative 苏州大学 2021-12-10 CN disclosed
CN-113636977-A Synthesis method of 2-aryl benzazepine and derivatives thereof 温州大学 2021-11-12 CN disclosed
WO-2021071843-A1 MUSCARINIC ACETYLCHOLINE M1 RECEPTOR ANTAGONISTS Pipeline Therapeutics, Inc. (US) 2021-04-15 WO disclosed
CN-112110801-A Method for synthesizing gamma-aryl substituted ketone compound 浙江工业大学 2020-12-22 CN disclosed
CN-108285415-B Preparation method of 1, 5-diketone compound 浙江师范大学 2020-06-02 CN disclosed
CN-108299198-B Preparation method of 1, 4-diketone compound 浙江师范大学 2020-04-17 CN disclosed
CN-110218227-A A method of preparing aryl ketone derivatives 苏州大学 2019-09-10 CN disclosed
CN-108299198-A A kind of preparation method of 1,4- dione compounds 浙江师范大学 2018-07-20 CN disclosed
CN-108285415-A A kind of preparation method of 1,5- dione compounds 浙江师范大学 2018-07-17 CN disclosed
WO-2018107415-A1 HYDROXY ISOXAZOLE COMPOUNDS USEFUL AS GPR120 AGONISTS MERCK SHARP & DOHME CORP. (US) 2018-06-21 WO disclosed
EP-2804868-B1 PYRAN-SPIROCYCLIC PIPERIDINE AMIDES AS MODULATORS OF ION CHANNELS VERTEX PHARMA (US) 2017-04-12 EP disclosed
EP-2686325-B1 MORPHOLINE-SPIROCYCLIC PIPERIDINE AMIDES AS MODULATORS OF ION CHANNELS VERTEX PHARMA (US) 2016-12-14 EP disclosed