SCHEMBL411643

SCHEMBL411643

CCOC(=O)CC(=O)Cc1cc(F)c(F)cc1F

nearest known ligand 0.44

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GAA P10253 2/20 0.44
MGAM O43451 1/20 0.44
SI P14410 1/20 0.44
MGAM2 Q2M2H8 1/20 0.44
NLRP3 Q96P20 2/20 0.39
KDM4E B2RXH2 3/20 0.38
MEN1 O00255 2/20 0.38
ALDH1A1 P00352 2/20 0.38
KMT2A Q03164 2/20 0.38
HDAC1 Q13547 2/20 0.37
HDAC3 O15379 1/20 0.37
HDAC2 Q92769 1/20 0.37
HDAC6 Q9UBN7 1/20 0.37
HDAC5 Q9UQL6 1/20 0.37
HSD17B10 Q99714 1/20 0.37
TDP1 Q9NUW8 1/20 0.36
DPP4 P27487 2/20 0.36
SMN1; SMN2 Q16637 1/20 0.36
HDAC8 Q9BY41 1/20 0.35
HTT P42858 1/20 0.35

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
SCHEMBL28259907 0.88 FAAH (0.40) ALDH1A1HDAC1DPP4SMN1; SMN2HDAC8
SCHEMBL30620176 0.86 KMT2A (0.43) GAAMGAMSIMGAM2NLRP3
SCHEMBL15490071 0.86 KMT2A (0.43) GAAMGAMSIMGAM2NLRP3
SCHEMBL18751641 0.86 FAAH (0.45) MEN1ALDH1A1KMT2ATDP1SMN1; SMN2
SCHEMBL27791252 0.86 MGAM (0.33) GAAMGAMSIMGAM2NLRP3
SCHEMBL725284 0.85 DPP4 (0.41) GAAMGAMSIMGAM2MEN1
SCHEMBL30167907 0.85 DPP4 (0.41) GAAMGAMSIMGAM2MEN1
SCHEMBL28482640 0.84 FAAH (0.54)
SCHEMBL5643889 0.83 ALDH1A1 (0.47) GAAMGAMSIMGAM2MEN1
SCHEMBL5567382 0.83 MAPT (0.42) GAAMGAMSIMGAM2NLRP3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2021118137-A1 METHOD FOR ENZYMATICALLY PRODUCING BETA AMINO ACID USING NOVEL ESTER HYDROLASE 건국대학교 산학협력단 2021-06-17 WO claimed
CN-119039260-A Epigenetic medicine for enhancing anticancer effect of pali antitumor agent and application thereof 山东铂源药业股份有限公司 2024-11-29 CN disclosed
CN-116947638-A Method for preparing sitagliptin intermediate by one-pot method 淄博飞源化工有限公司 2023-10-27 CN disclosed
CN-116622658-A Beta-amino acid dehydrogenase mutant and application thereof in synthesis of aromatic beta-amino acid compound 中国科学院天津工业生物技术研究所 2023-08-22 CN disclosed
CN-115583935-A Preparation method of 4- (2, 4, 5-trifluorophenyl) -3-oxybutyrate ester 浙江工业大学 2023-01-10 CN disclosed
CN-113846131-A Method for preparing (R) -3-amino-4- (2,4, 5-trifluorophenyl) -butyric acid 尚科生物医药(上海)有限公司 2021-12-28 CN disclosed
WO-2021118137-A1 METHOD FOR ENZYMATICALLY PRODUCING BETA AMINO ACID USING NOVEL ESTER HYDROLASE 건국대학교 산학협력단 2021-06-17 WO disclosed
WO-2021118137-A1 METHOD FOR ENZYMATICALLY PRODUCING BETA AMINO ACID USING NOVEL ESTER HYDROLASE 건국대학교 산학협력단 2021-06-17 WO disclosed
EP-3156391-B1 METHOD FOR PREPARING SITAGLIPTIN INTERMEDIATE VIA ASYMMETRICAL REDUCTION METHOD ZHEJIANG HUAHAI PHARM CO LTD (CN) 2020-09-02 EP disclosed
CN-107311862-B Preparation method of sitagliptin intermediate 南京红杉生物科技有限公司 2020-06-19 CN disclosed
US-20100273786-A1 TETRAHYDRO-IMIDAZ0[1,5-A]PYRAZINE DERIVATIVES, PREPARATION PROCESS AND MEDICINAL USE THEREOF JIANGSU HENGRUI MEDICINE CO., LTD. (CN) 2010-10-28 US disclosed
US-20100273786-A1 TETRAHYDRO-IMIDAZ0[1,5-A]PYRAZINE DERIVATIVES, PREPARATION PROCESS AND MEDICINAL USE THEREOF JIANGSU HENGRUI MEDICINE CO., LTD. (CN) 2010-10-28 US disclosed
US-20100273786-A1 TETRAHYDRO-IMIDAZ0[1,5-A]PYRAZINE DERIVATIVES, PREPARATION PROCESS AND MEDICINAL USE THEREOF JIANGSU HENGRUI MEDICINE CO., LTD. (CN) 2010-10-28 US disclosed
EP-2230241-A1 TETRAHYDRO-IMIDAZOÝ1,5-A¨PYRAZINE DERIVATIVES, PREPARATION METHODS AND MEDICAL USES THEREOF Jiangsu Hengrui Medicine Co., Ltd. (CN) 2010-09-22 EP disclosed
EP-2230241-A1 TETRAHYDRO-IMIDAZOÝ1,5-A¨PYRAZINE DERIVATIVES, PREPARATION METHODS AND MEDICAL USES THEREOF Jiangsu Hengrui Medicine Co., Ltd. (CN) 2010-09-22 EP disclosed
CN-101641361-A Tetrahydroimidazo [1, 5-a ] pyrazine derivative, preparation method and application thereof in medicine SHANGHAI HENGRUI PHARM CO LTD 2010-02-03 CN disclosed
CN-101641360-A Piperazine derivatives, preparation method and medical application thereof SHANGHAI HENGRUI PHARM CO LTD 2010-02-03 CN disclosed
US-20090192326-A1 Preparation of sitagliptin intermediate TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2009-07-30 US disclosed
US-20090192326-A1 Preparation of sitagliptin intermediate TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2009-07-30 US disclosed
WO-2009064476-A1 PREPARATION OF SITAGLIPTIN INTERMEDIATE TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2009-05-22 WO 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-20090192326-A1 Preparation of sitagliptin intermediate DPP4, DPP7, DPP3 GAA 609/4885MGAM 472/4885SI 7/4885
US-20100273786-A1 TETRAHYDRO-IMIDAZ0[1,5-A]PYRAZINE DERIVATIVES, PREPARATION PROCESS AND MEDICINAL USE THEREOF DPP4, DPP7, DPP3 GAA 247/4885MGAM 198/4885SI 28/4885

“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.