SCHEMBL275775

SCHEMBL275775

COC(=O)CC(=O)c1ccccc1

nearest known ligand 0.67

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ KMT2A Q03164 7/20 0.67
▸ MEN1 O00255 6/20 0.67
▸ HPGD P15428 4/20 0.67
▸ SMN1; SMN2 Q16637 4/20 0.67
▸ MAPT P10636 3/20 0.67
▸ CYP3A4 P08684 2/20 0.67
▸ KDM4E B2RXH2 2/20 0.67
▸ MAPK1 P28482 2/20 0.67
▸ ALOX15 P16050 1/20 0.67
▸ CES1 P23141 1/20 0.67
▸ TDP1 Q9NUW8 1/20 0.67
▸ NPC1 O15118 6/20 0.59
▸ RAB9A P51151 6/20 0.59
▸ PTPN1 P18031 2/20 0.57
▸ ERCC5 P28715 1/20 0.57
▸ FEN1 P39748 1/20 0.57
▸ TSHR P16473 1/20 0.56
▸ ALDH1A1 P00352 5/20 0.53
▸ HIF1A Q16665 2/20 0.53
▸ PLOD2 O00469 1/20 0.53

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
SCHEMBL29035576 0.98 KMT2A (0.64) KMT2AMEN1HPGDSMN1; SMN2MAPT
SCHEMBL23466830 0.90 KMT2A (0.59) KMT2AMEN1HPGDSMN1; SMN2MAPT
SCHEMBL28018774 0.89 KMT2A (0.54) KMT2AMEN1HPGDSMN1; SMN2MAPT
SCHEMBL3821582 0.88 ERCC5 (0.62) KMT2AMEN1HPGDSMN1; SMN2MAPT
Pyrrolidine SCHEMBL28657706 0.86 KMT2A (0.50) KMT2AMEN1HPGDSMN1; SMN2MAPT
SCHEMBL1728532 0.85 ERCC5 (0.68) KMT2AHPGDSMN1; SMN2MAPTNPC1
SCHEMBL14918369 0.85 CA1 (0.52) KMT2AMEN1HPGDSMN1; SMN2MAPT
SCHEMBL636225 0.84 KMT2A (0.70) KMT2AMEN1HPGDSMN1; SMN2MAPT
SCHEMBL3252460 0.84 KMT2A (0.70) KMT2AMEN1HPGDSMN1; SMN2MAPT
SCHEMBL135356 0.83 NR4A2 (0.61) KMT2AMEN1HPGDSMN1; SMN2MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119930684-A C (C)2Symmetrical N-axis chiral bisindole diphosphine ligand and preparation method and application thereof 青岛大学 2025-05-06 — — CN claimed
CN-119751460-A Triazolopyrimidine antitumor compound and preparation method and application thereof 江苏海洋大学 2025-04-04 — — CN claimed
CN-107876092-B Application of titanium catalyst with cyclic structure as reaction catalyst for synthesizing benzyl carbonate or diphenyl carbonate by ester exchange 华东理工大学 2023-01-10 — — CN claimed
CN-115160943-A High-temperature-resistant optical lens protective film and production process 苏州纽劢特新材料科技有限公司 2022-10-11 — — CN claimed
CN-113533253-A Refractive index matching fluid and application thereof in optical detection of glass 光华科学技术研究院(广东)有限公司 2021-10-22 — — CN claimed
CN-113324736-A Refractive index matching fluid and optical detection method of glass 光华科学技术研究院(广东)有限公司 2021-08-31 — — CN claimed
CN-107876092-A The high stability titanium catalyst of ester exchange carbonate synthesis benzene methyl and diphenyl carbonate 华东理工大学 2018-04-06 — — CN claimed
CN-106478443-B The method that difluoro Ya Jia Ji Phosphonium inner salts are used to synthesize β keto-amides as new ammonolysis reagent 四川理工学院 2018-04-03 — — CN claimed
CN-105753682-B A kind of preparation method of phenylcyclopentyl ketone 中国科学院成都有机化学有限公司 2018-01-09 — — CN claimed
CN-104803934-B A kind of phenyl-isoxazole triazole carboxylic acid's class compound and its synthetic method and application with antitumor activity 陕西科技大学 2018-01-02 — — CN claimed
CN-106478443-A The method that difluoro methylene inner salt is used for synthesizing β keto-amide as new ammonolysis reagent 四川理工学院 2017-03-08 — — CN claimed
CN-101657759-B Alkali-developable photosensitive resin composition and beta-diketone ADEKA CORP 2012-07-25 — — CN claimed
CN-102516210-A Preparation method of 2,3-dicyanofuran compound UNIV EAST CHINA SCIENCE & TECH 2012-06-27 — — CN claimed
US-20080262247-A1 Process for preparing arylaminopropanols ECKERT MARKUS 2008-10-23 — — US claimed
US-20030225153-A1 Process for preparing arylaminopropanols LANXESS DEUTSCHLAND GMBH (DE) 2003-12-04 — — US claimed
CN-1445224-A Process for preparing arylaminopropanols BAYER AG (DE) 2003-10-01 — — CN claimed
EP-1346977-A1 Method for producing aryl-aminopropanols Bayer Aktiengesellschaft (DE) 2003-09-24 — — EP claimed
EP-0417555-B1 Pentamethine dyes and derivatives BAYER AG (DE) 1993-11-03 — — EP claimed
US-5118814-A Pressure sensitive and heat sensitive recording media BAYER AKTIENGESELLSCHAFT (DE) 1992-06-02 — — US claimed
EP-0417555-A1 Pentamethine dyes and derivatives BAYER AG (DE) 1991-03-20 — — EP claimed

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-20030225153-A1 Process for preparing arylaminopropanols AHR, CYP1A1, CYP1A2 KMT2A 746/4885MEN1 3279/4885HPGD 1504/4885
US-20080262247-A1 Process for preparing arylaminopropanols CYP1A1, CYP1A2, AHR KMT2A 1021/4885MEN1 2931/4885HPGD 1119/4885

“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.

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