SCHEMBL1283604

SCHEMBL1283604

CC(=O)c1ccc(Oc2ccc(Cl)cc2)cc1

nearest known ligand 0.79

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HPGD P15428 4/20 0.79
MAPT P10636 2/20 0.79
RAB9A P51151 2/20 0.79
MAOA P21397 3/20 0.64
MAOB P27338 3/20 0.64
SMN1; SMN2 Q16637 3/20 0.56
HTT P42858 2/20 0.56
KMT2A Q03164 2/20 0.56
MEN1 O00255 1/20 0.56
NPC1 O15118 1/20 0.56
NLRP1 Q9C000 1/20 0.56
L3MBTL1 Q9Y468 1/20 0.52
MMP1 P03956 2/20 0.51
ESRRA P11474 1/20 0.51
GAA P10253 1/20 0.50
STS P08842 1/20 0.48
ALDH1A1 P00352 2/20 0.48
TSHR P16473 1/20 0.48
PARP15 Q460N3 1/20 0.48
PARP14 Q460N5 1/20 0.48

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
SCHEMBL3301210 0.89 HPGD (1.00) HPGDMAPTRAB9AMAOBSMN1; SMN2
SCHEMBL203697 0.89 HPGD (1.00) HPGDMAPTRAB9AMAOBSMN1; SMN2
SCHEMBL75640 0.87 MAPT (0.69) HPGDMAPTRAB9AMAOAMAOB
SCHEMBL28193245 0.87 MAPT (0.69) HPGDMAPTRAB9AMAOAMAOB
SCHEMBL17187946 0.87 MAPT (0.69) HPGDMAPTRAB9AMAOAMAOB
SCHEMBL13252903 0.85 HPGD (0.58) HPGDMAPTRAB9AMAOAMAOB
Hydrochloric Acid SCHEMBL27858043 0.84 MAPT (0.67) HPGDMAPTRAB9AMAOAMAOB
Ammonia Solution, Strong SCHEMBL17180520 0.84 MAPT (0.67) HPGDMAPTRAB9AMAOAMAOB
SCHEMBL20836631 0.83 HPGD (0.79) HPGDMAPTRAB9AMAOAMAOB
SCHEMBL9789228 0.83 MAPT (0.86) HPGDMAPTRAB9AMAOBSMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-112409142-B Preparation method of 4-p-chlorophenoxyl acetophenone compounds 帕潘纳(北京)科技有限公司 2022-04-19 CN claimed
CN-112409142-A Preparation method of 4-p-chlorophenoxyl acetophenone compounds 帕潘纳(北京)科技有限公司 2021-02-26 CN claimed
EP-0986540-B1 THE USE OF CARBOCYCLIC AND HETEROCYCLIC SUBSTITUTED SEMICARBAZONES AND THIOSEMICARBAZONES AS SODIUM CHANNEL BLOCKERS EURO CELTIQUE SA (LU) 2005-02-16 EP claimed
US-6696442-B2 THERAPY OF DISORDER RESPONSIVE TO THE BLOCKADE OF SODIUM CHANNELS IN A MAMMAL SUFFERING THEREFROM BY ADMINISTERING CARBOCYCLIC AND HETEROCYCLIC SUBSTITUTED SEMICARBAZONES AND THIOSEMICARBAZONES, WHICH ACT AS BLOCKERS OF SODIUM CHANNELS EURO-CELTIQUE S.A. (LU) 2004-02-24 US claimed
US-20030225080-A1 Carbocyclic and heterocyclic substituted semicarbazones and thiosemicarbazones and the use thereof EURO-CELTIQUES S.A. 2003-12-04 US claimed
US-6613803-B1 Treating, preventing or ameliorating pain EURO-CELTIQUE S.A. (LU) 2003-09-02 US claimed
US-20020183321-A1 Carbocyclic and heterocyclic substituted semicarbazones and thiosemicarbazones and the use thereof COCENSYS, INC. 2002-12-05 US claimed
US-20020061886-A1 Carbocyclic and heterocyclic substituted semicarbazones and thiosemicarbazones and the use thereof COCENSYS, INC. 2002-05-23 US claimed
CN-113666819-B Method for preparing penconazole intermediate 帕潘纳(北京)科技有限公司 2024-06-21 CN disclosed
CN-114456048-B Preparation method of penconazole intermediate 帕潘纳(北京)科技有限公司 2024-02-02 CN disclosed
CN-114539041-B Preparation method of penconazole intermediate 帕潘纳(北京)科技有限公司 2024-01-05 CN disclosed
CN-116018138-A Substituted 1H-imidazo [1,2-b ] pyrazole-3-carboxamides as inhibitors of brunauer tyrosine kinase 河南知微生物医药有限公司 2023-04-25 CN disclosed
CN-114539041-A Preparation method of chlorofluoroether ipconazole intermediate 帕潘纳(北京)科技有限公司 2022-05-27 CN disclosed
CN-114456048-A Preparation method of chlorofluoromethane intermediate 帕潘纳(北京)科技有限公司 2022-05-10 CN disclosed
EP-0065485-A2 Arylphenyl ether derivatives as microbicides, process for their preparation and their application CIBA-GEIGY AG (CH) 1982-11-24 EP disclosed
US-4287213-A Dichloroacyl diphenyl ether mite ovacides CHEVRON RESEARCH COMPANY (US) 1981-09-01 US disclosed
US-4196215-A Alkyne compounds and method of use MERCK PATENT GESELLSCHAFT MIT BESCHRAENKTER HAFTUNG (DE) 1980-04-01 US disclosed
US-4136200-A PHENYLBUTANOL DERIVATIVES, PROCESSES FOR THEIR PREPARATION AND COMPOSITIONS CONTAINING THEM MERCK PATENT GESELLSCHAFT MIT BESCHRANKTER HAFTUNG (DE) 1979-01-23 US disclosed
US-4115456-A Alkyne compounds and method of use MERCK PATENT GESELLSCHAFT MIT BESCHRANKTER HAFTUNG (DE) 1978-09-19 US disclosed
US-4049823-A Phenylbutanol derivatives and compositions containing them MERCK PATENT GESELLSCHAFT MIT BESCHRANKTER HAFTUNG (DT) 1977-09-20 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 (3 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-20030225080-A1 Carbocyclic and heterocyclic substituted semicarbazones and thiosemicarbazones and the use thereof GLRB, SLC1A1, SOD1 HPGD 1599/4885MAPT 2250/4885RAB9A 4389/4885
US-20020061886-A1 Carbocyclic and heterocyclic substituted semicarbazones and thiosemicarbazones and the use thereof GLRB, SLC1A1, SOD1 HPGD 1599/4885MAPT 2250/4885RAB9A 4389/4885
US-20020183321-A1 Carbocyclic and heterocyclic substituted semicarbazones and thiosemicarbazones and the use thereof GLRB, CBR1, ALDH1A2 HPGD 1752/4885MAPT 2452/4885RAB9A 4404/4885

“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.