SCHEMBL1699595

SCHEMBL1699595

CC(=O)Cc1ccc(F)c(Cl)c1

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PIK3CA P42336 1/20 0.56
TSHR P16473 2/20 0.46
CNR2 P34972 1/20 0.45
CA2 P00918 1/20 0.44
RPA1 P27694 1/20 0.44
HDAC3 O15379 1/20 0.43
HDAC1 Q13547 1/20 0.43
HDAC2 Q92769 1/20 0.43
HDAC6 Q9UBN7 1/20 0.43
KDM4E B2RXH2 1/20 0.43
KCNJ6 P48051 1/20 0.43
KCNJ5 P48544 1/20 0.43
KCNJ3 P48549 1/20 0.43
ALDH1A1 P00352 1/20 0.43
MAPT P10636 1/20 0.43
ALOX15 P16050 1/20 0.43
MEN1 O00255 2/20 0.42
KMT2A Q03164 2/20 0.42
NPC1 O15118 2/20 0.41
LMNA P02545 2/20 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
SCHEMBL13567915 0.85 ANO1 (0.44) PIK3CATSHRCA2MAPT
SCHEMBL869116 0.83 CA2 (0.65) PIK3CATSHRCA2RPA1HDAC3
SCHEMBL21090110 0.83 PIK3CA (0.58) PIK3CATSHRCNR2CA2RPA1
SCHEMBL1699590 0.82 MAOA (0.50) PIK3CAALDH1A1HTT
SCHEMBL1136782 0.82 TSHR (0.53) PIK3CATSHRCA2KMT2ASMN1; SMN2
SCHEMBL23869399 0.82 PIK3CA (0.54) PIK3CATSHRCNR2CA2RPA1
SCHEMBL10272184 0.81 PIK3CA (0.49) PIK3CATSHRCNR2CA2RPA1
SCHEMBL27835202 0.81 PIK3CA (0.56) PIK3CATSHRCNR2CA2RPA1
SCHEMBL11520973 0.81 PIK3CA (0.56) PIK3CATSHRCNR2CA2RPA1
SCHEMBL3396522 0.81 PIK3CA (0.56) PIK3CATSHRCA2RPA1HDAC3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117623893-A Preparation method of 5-hydroxy-1-indenone 阜新清稷升科技有限公司 2024-03-01 CN claimed
CN-117623893-A Preparation method of 5-hydroxy-1-indenone 阜新清稷升科技有限公司 2024-03-01 CN disclosed
CN-117623893-A Preparation method of 5-hydroxy-1-indenone 阜新清稷升科技有限公司 2024-03-01 CN disclosed
US-20230357165-A1 QUINAZOLINONES DERIVATIVES FOR TREATMENT OF NON-ALCOHOLIC FATTY LIVER DISEASE, PREPARATION AND USE THEREOF COUNCIL OF SCIENTIFIC & INDUSTRIAL RESEARCH (IN) 2023-11-09 US disclosed
EP-2588450-B1 NAPHT-2-YLACETIC ACID DERIVATIVES TO TREAT AIDS GILEAD SCIENCES INC (US) 2017-05-24 EP disclosed
EP-2588450-B1 NAPHT-2-YLACETIC ACID DERIVATIVES TO TREAT AIDS GILEAD SCIENCES INC (US) 2017-05-24 EP disclosed
CN-103980184-B Piperidine compounds, medical composition and its use containing this compound 爱思开生物制药株式会社 2016-08-24 CN disclosed
US-9102614-B2 Naphth-2-ylacetic acid derivatives to treat AIDS GILEAD SCIENCES, INC. (US) 2015-08-11 US disclosed
US-9102614-B2 Naphth-2-ylacetic acid derivatives to treat AIDS GILEAD SCIENCES, INC. (US) 2015-08-11 US disclosed
US-9102614-B2 Naphth-2-ylacetic acid derivatives to treat AIDS GILEAD SCIENCES, INC. (US) 2015-08-11 US disclosed
US-20130203727-A1 NAPHT-2-YLACETIC ACID DERIVATIVES TO TREAT AIDS GILEAD SCIENCES, INC. (US) 2013-08-08 US disclosed
US-20130203727-A1 NAPHT-2-YLACETIC ACID DERIVATIVES TO TREAT AIDS GILEAD SCIENCES, INC. (US) 2013-08-08 US disclosed
US-20130203727-A1 NAPHT-2-YLACETIC ACID DERIVATIVES TO TREAT AIDS GILEAD SCIENCES, INC. (US) 2013-08-08 US disclosed
EP-2588450-A1 NAPHT- 2 -YLACETIC ACID DERIVATIVES TO TREAT AIDS Gilead Sciences, Inc. (US) 2013-05-08 EP disclosed
CN-101133037-B Six-membered heterocyclic compound and use thereof ASAHI KASEI PHARMA CORP 2012-05-09 CN disclosed
WO-2012003497-A1 NAPHT- 2 -YLACETIC ACID DERIVATIVES TO TREAT AIDS GILEAD SCIENCES, INC. (US) 2012-01-05 WO disclosed
WO-2012003497-A1 NAPHT- 2 -YLACETIC ACID DERIVATIVES TO TREAT AIDS GILEAD SCIENCES, INC. (US) 2012-01-05 WO disclosed
CN-102186840-A Piperidine compounds, pharmaceutical compositions containing the same and uses thereof SK HOLDINGS CO LTD 2011-09-14 CN disclosed
CN-101133037-A Six-membered heterocyclic compound and use thereof ASAHI KASEI PHARMA CORP (JP) 2008-02-27 CN disclosed
CN-1124960-A Indole derivatives as 5-HT1A and/or 5-HT2 ligands BOEHRINGER INGELHEIM ITALIA (IT) 1996-06-19 CN 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-20230357165-A1 QUINAZOLINONES DERIVATIVES FOR TREATMENT OF NON-ALCOHOLIC FATTY LIVER DISEASE, PREPARATION AND USE THEREOF ATG7, GOT1, LIPC PIK3CA 2562/4885TSHR 4173/4885CNR2 3626/4885
US-20130203727-A1 NAPHT-2-YLACETIC ACID DERIVATIVES TO TREAT AIDS NFATC1, AADAT, ACAT1 PIK3CA 2901/4885TSHR 4399/4885CNR2 3585/4885

“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.