SCHEMBL1455828

SCHEMBL1455828

CCOC(=O)C(C)C(=O)OC(C)(C)C

nearest known ligand 0.42

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP1A2 P05177 1/20 0.41
CYP2C9 P11712 1/20 0.41
CYP2C19 P33261 1/20 0.41
HTT P42858 1/20 0.41
ALDH1A1 P00352 4/20 0.39
HPGD P15428 1/20 0.39
MMP8 P22894 1/20 0.38
NOS1 P29475 2/20 0.37
NOS3 P29474 1/20 0.37
NOS2 P35228 1/20 0.37
LMNA P02545 1/20 0.37
HSD17B10 Q99714 1/20 0.37
ALOX15 P16050 1/20 0.36
MGAM O43451 1/20 0.36
GAA P10253 1/20 0.36
SI P14410 1/20 0.36
MGAM2 Q2M2H8 1/20 0.36
SOAT1 P35610 1/20 0.36
CA1 P00915 1/20 0.35
CA2 P00918 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
SCHEMBL526638 0.86 NOS1 (0.40) NOS1NOS3NOS2LMNAGAA
SCHEMBL141446 0.83 ALDH1A1 (0.53) CYP2C19ALDH1A1HPGDMMP8LMNA
SCHEMBL28186389 0.81 ALDH1A1 (0.50) CYP2C19ALDH1A1HPGDMMP8LMNA
Ethane SCHEMBL9181718 0.81 ALDH1A1 (0.50) CYP2C19ALDH1A1HPGDMMP8LMNA
SCHEMBL8800602 0.81 ALDH1A1 (0.50) CYP2C19ALDH1A1HPGDMMP8LMNA
Ammonia Solution, Strong SCHEMBL28791130 0.81 ALDH1A1 (0.50) CYP2C19ALDH1A1HPGDMMP8LMNA
SCHEMBL27800508 0.81 NOS1 (0.40) NOS1NOS3NOS2LMNAGAA
SCHEMBL1661987 0.80 CYP1A2 (0.41) CYP1A2CYP2C9CYP2C19HTTALDH1A1
SCHEMBL9847861 0.78 CA1 (0.35) CYP1A2CYP2C9CYP2C19HTTMMP8
SCHEMBL3953356 0.78 CYP1A2 (0.38) CYP1A2CYP2C9CYP2C19HTTALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2001072704-A1 AZETIDINONE DERIVATIVES, A PROCESS FOR THEIR PREPARATION AND A METHOD FOR PRODUCING 1-β-ALKYL AZETIDINONE USING THE SAME DAEWOONG PHARMACEUTICAL CO., LTD. (KR) 2001-10-04 WO claimed
US-9834527-B2 Macrocyclic urea derivatives as inhibitors of TAFIa, their preparation and their use as pharmaceuticals SANOFI (FR) 2017-12-05 US disclosed
EP-3027611-B1 MACROCYCLIC UREA DERIVATIVES AS INHIBITORS OF TAFI A, THEIR PREPARATION AND THEIR USE AS PHARMACEUTICALS SANOFI SA (FR) 2017-07-26 EP disclosed
EP-3027611-A1 MACROCYCLIC UREA DERIVATIVES AS INHIBITORS OF TAFI A, THEIR PREPARATION AND THEIR USE AS PHARMACEUTICALS SANOFI (FR) 2016-06-08 EP disclosed
US-20160137618-A1 Macrocyclic Urea Derivatives as Inhibitors of TAFIa, Their Preparation and Their Use as Pharmaceuticals SANOFI (FR) 2016-05-19 US disclosed
CN-105263928-A Macrocyclic urea derivatives as inhibitors of TAFIa, their preparation and their use as medicaments SAI NUOFEI 2016-01-20 CN disclosed
WO-2014198620-A1 MACROCYCLIC UREA DERIVATIVES AS INHIBITORS OF TAFIA, THEIR PREPARATION AND THEIR USE AS PHARMACEUTICALS SANOFI (FR) 2014-12-18 WO disclosed
US-20120172392-A1 AMINE-BASED AND AMIDE-BASED INHIBITORS OF SEMICARBAZIDE-SENSITIVE AMINE OXIDASE (SSAO) ENZYME ACTIVITY AND VAP-1 MEDIATED ADHESION USEFUL FOR TREATMENT OF DISEASES SALTER-CID LUISA M (US) 2012-07-05 US disclosed
US-20120172392-A1 AMINE-BASED AND AMIDE-BASED INHIBITORS OF SEMICARBAZIDE-SENSITIVE AMINE OXIDASE (SSAO) ENZYME ACTIVITY AND VAP-1 MEDIATED ADHESION USEFUL FOR TREATMENT OF DISEASES SALTER-CID LUISA M (US) 2012-07-05 US disclosed
US-20120172392-A1 AMINE-BASED AND AMIDE-BASED INHIBITORS OF SEMICARBAZIDE-SENSITIVE AMINE OXIDASE (SSAO) ENZYME ACTIVITY AND VAP-1 MEDIATED ADHESION USEFUL FOR TREATMENT OF DISEASES SALTER-CID LUISA M (US) 2012-07-05 US disclosed
WO-2001072704-A1 AZETIDINONE DERIVATIVES, A PROCESS FOR THEIR PREPARATION AND A METHOD FOR PRODUCING 1-β-ALKYL AZETIDINONE USING THE SAME DAEWOONG PHARMACEUTICAL CO., LTD. (KR) 2001-10-04 WO disclosed
EP-0546742-B1 4-(1,1-Dialkoxycarbonyl-alkyl)azetidin-2-one derivatives and synthesis of 4-(1-carboxy-alkyl)azetidin-2-one derivatives therefrom TAKASAGO PERFUMERY CO LTD (JP) 2001-06-20 EP disclosed
WO-2000066557-A1 NEW COMPOUNDS ASTRAZENECA AB (SE) 2000-11-09 WO disclosed
US-5574152-A 4-(1,1-dialkoxycarbonylalkyl) azetidin-2-one derivative and process for producing 4-(1-carboxyalkyl) azetidin-2-one derivative using the same TAKASAGO INTERNATIONAL CORPORATION (JP) 1996-11-12 US disclosed
US-5371214-A 4-(1,1-dialkoxycarbonylalkyl)azetidin-2-one derivative and process for producing 4-(1-carboxyalkyl)azetidin-2-one derivative using the same TAKASAGO INTERNATIONAL CORPORATION (JP) 1994-12-06 US disclosed
EP-0546742-A1 4-(1,1-Dialkoxycarbonyl-alkyl)azetidin-2-one-derivatives and synthesis of 4-(1-carboxy-alkyl)azetidin-2-one derivatives therefrom Takasago International Corporation (JP) 1993-06-16 EP disclosed
CN-1008817-B Process for preparing fluoroallylamine derivatives MERRELL DOW PHARMACEVTICALS IN (US) 1990-07-18 CN disclosed
EP-0168013-B1 FLUOROALLYLAMINE DERIVATIVES MERRELL DOW PHARMACEUTICALS INC. (US) 1988-03-02 EP disclosed
US-4699928-A ANTIDEPRESSANTS, TREATMENT OF PARKINSON'S DISEASE MERRELL DOW PHARMACEUTICALS INC. (US) 1987-10-13 US disclosed
EP-0168013-A1 Fluoroallylamine derivatives MERRELL DOW PHARMACEUTICALS INC. (US) 1986-01-15 EP 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-20160137618-A1 Macrocyclic Urea Derivatives as Inhibitors of TAFIa, Their Preparation and Their Use as Pharmaceuticals TFPI, TFPI2, F12 CYP1A2 731/4885CYP2C9 375/4885CYP2C19 399/4885
US-20120172392-A1 AMINE-BASED AND AMIDE-BASED INHIBITORS OF SEMICARBAZIDE-SENSITIVE AMINE OXIDASE (SSAO) ENZYME ACTIVITY AND VAP-1 MEDIATED ADHESION USEFUL FOR TREATMENT OF DISEASES VCAM1, AOC2, AOC1 CYP1A2 2016/4885CYP2C9 3363/4885CYP2C19 3886/4885

“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.