SCHEMBL2071865

SCHEMBL2071865

Cc1cc(C)cc(OC(N)=O)c1

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 2/20 0.52
KMT2A Q03164 2/20 0.52
MAPT P10636 1/20 0.44
THRB P10828 1/20 0.44
ALDH1A1 P00352 3/20 0.43
TSHR P16473 2/20 0.43
CYP3A4 P08684 1/20 0.43
MAPK1 P28482 1/20 0.43
TDP1 Q9NUW8 1/20 0.43
TPMT P51580 1/20 0.41
LMNA P02545 2/20 0.41
PARP10 Q53GL7 1/20 0.41
SMN1; SMN2 Q16637 1/20 0.40
PRSS1 P07477 1/20 0.39
PRSS2 P07478 1/20 0.39
C1S P09871 1/20 0.39
PRSS3 P35030 1/20 0.39
HPGD P15428 2/20 0.39
HTT P42858 1/20 0.38
KIF11 P52732 1/20 0.37

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
SCHEMBL29177324 0.86 MEN1 (0.44) MEN1KMT2AMAPTTHRBALDH1A1
SCHEMBL8999515 0.86 KMT2A (0.44) MEN1KMT2AMAPTTHRBALDH1A1
SCHEMBL28362239 0.86 MEN1 (0.44) MEN1KMT2AMAPTTHRBALDH1A1
Tromethamine SCHEMBL1645080 0.85 MEN1 (0.40) MEN1KMT2AMAPTTHRBALDH1A1
SCHEMBL11463871 0.82 RXRB (0.41) MEN1KMT2AMAPTTHRBTDP1
SCHEMBL26090155 0.81 MGLL (0.45) MEN1KMT2AMAPTTHRBPARP10
SCHEMBL3829975 0.80 MEN1 (0.48) MEN1KMT2AMAPTTHRBALDH1A1
SCHEMBL9721680 0.79 KMT2A (0.50) MEN1KMT2AALDH1A1TSHRCYP3A4
SCHEMBL5700033 0.79 KMT2A (0.73) MEN1KMT2AMAPTALDH1A1CYP3A4
SCHEMBL22980920 0.78 TPMT (0.48) MEN1KMT2AMAPTTHRBALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118311186-A Method for measuring Wu Pa tenib intermediate and enantiomer thereof by liquid chromatography 山东百诺医药股份有限公司 2024-07-09 CN claimed
CN-117630224-A Method for separating and measuring non-neridrone enantiomer by HPLC 安徽联创生物医药股份有限公司 2024-03-01 CN claimed
CN-113680336-B Cellulose coated spherical covalent organic framework chiral stationary phase and application 华南师范大学 2024-01-30 CN claimed
CN-116609445-A Acyclic nucleoside phosphonate compound and preparation method, analysis method and application thereof 上海医药工业研究院有限公司 2023-08-18 CN claimed
CN-114264762-B High performance liquid chromatography separation detection method for key intermediate enantiomer of tergolian praziquantel 上海柏狮生物科技有限公司 2023-08-18 CN claimed
CN-115963217-A Method for detecting imidapril intermediate and impurities 北京阳光诺和药物研究股份有限公司 2023-04-14 CN claimed
CN-115825284-A Method for separating rivaroxaban intermediate and impurities thereof and detecting content of each component 重庆华邦制药有限公司 2023-03-21 CN claimed
CN-115616104-A Method for detecting enantiomer of dexmedetomidine hydrochloride injection 山西远扬医药科技有限公司 2023-01-17 CN claimed
CN-115541733-A Method for measuring protected amino acid enantiomer by reverse phase chromatography 南京锐志生物医药有限公司 2022-12-30 CN claimed
CN-115541731-A Analysis method for protecting enantiomer of amino acid 南京锐志生物医药有限公司 2022-12-30 CN claimed
EP-1944606-A2 Method of analyzing optical purity of 1-Chloro-3, 5-Ditoluyl-2-Deoxy-L-Ribose using (S)-Tetrahydro-3-Furanol Samchully Pharm. Co., Ltd. (KR) 2008-07-16 EP claimed
US-20050065207-A1 Method for the preparation of escitalopram H. LUNDBECK A/S (DK) 2005-03-24 US claimed
EP-0975560-A4 CHIRAL SEPARATIONS OF AMINO ACIDS CHIRAL TECHNOLOGIES INC (US) 2004-10-06 EP claimed
EP-1070076-A4 CHIRAL SEPARATIONS OF PYRIMIDINES CHIRAL TECHNOLOGIES INC (US) 2002-05-29 EP claimed
EP-1070076-A1 CHIRAL SEPARATIONS OF PYRIMIDINES Chiral Technologies, Inc. (US) 2001-01-24 EP claimed
US-6130353-A Chiral separations of amino acids CHIRAL TECHNOLOGIES, INC. (US) 2000-10-10 US claimed
EP-0975560-A1 CHIRAL SEPARATIONS OF AMINO ACIDS Chiral Technologies, Inc. (US) 2000-02-02 EP claimed
WO-1999047531-A1 CHIRAL SEPARATIONS OF PYRIMIDINES CHIRAL TECHNOLOGIES, INC. (US) 1999-09-23 WO claimed
WO-1998041489-A1 CHIRAL SEPARATIONS OF AMINO ACIDS CHIRAL TECHNOLOGIES, INC. (US) 1998-09-24 WO claimed
US-5811532-A BOUND THROUGH A SPACER TO THE SURFACE HYDROXYL GROUPS OF A REFRACTORY INORGANIC OXIDE UOP LLC (US) 1998-09-22 US 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 (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-20050065207-A1 Method for the preparation of escitalopram SLC6A4, GSK3B, GSK3A MEN1 3845/4885KMT2A 2125/4885MAPT 1101/4885

“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.