SCHEMBL3787744

SCHEMBL3787744

O=C(O)C1C2C=CC(C2)C1C(=O)OC(=O)[C@H]1[C@@H](C(=O)O)[C@@H]2C=C[C@H]1C2

nearest known ligand 0.59

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
POLB P06746 4/20 0.59
ALDH1A1 P00352 3/20 0.59
SMN1; SMN2 Q16637 1/20 0.59
TDP1 Q9NUW8 2/20 0.54
APEX1 P27695 1/20 0.54
LMNA P02545 1/20 0.50
KDM4E B2RXH2 1/20 0.43
NPSR1 Q6W5P4 1/20 0.41
TAAR1 Q96RJ0 1/20 0.41
CASP6 P55212 1/20 0.41
CTDSP1 Q9GZU7 1/20 0.41
HSD17B10 Q99714 1/20 0.41
MEN1 O00255 1/20 0.41
KMT2A Q03164 1/20 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
SCHEMBL4665372 1.00 POLB (0.59) POLBALDH1A1SMN1; SMN2TDP1APEX1
SCHEMBL3777075 1.00 POLB (0.59) POLBALDH1A1SMN1; SMN2TDP1APEX1
SCHEMBL27495 1.00 POLB (0.59) POLBALDH1A1SMN1; SMN2TDP1APEX1
SCHEMBL572756 1.00 POLB (0.59) POLBALDH1A1SMN1; SMN2TDP1APEX1
SCHEMBL721693 0.87 POLB (0.74) POLBALDH1A1SMN1; SMN2TDP1APEX1
Alanine SCHEMBL15656219 0.86 POLB (0.48) POLBALDH1A1SMN1; SMN2TDP1APEX1
SCHEMBL23287488 0.86 POLB (0.70) POLBALDH1A1SMN1; SMN2TDP1APEX1
SCHEMBL381246 0.86 POLB (0.70) POLBALDH1A1SMN1; SMN2TDP1APEX1
SCHEMBL713506 0.86 POLB (0.70) POLBALDH1A1SMN1; SMN2TDP1APEX1
SCHEMBL24062391 0.86 POLB (0.70) POLBALDH1A1SMN1; SMN2TDP1APEX1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7795370-B2 Tetracarboxylic acid compound, polyimide thereof, and production method thereof MITSUBISHI CHEMICAL CORPORATION (JP) 2010-09-14 US disclosed
US-20090182114-A1 TETRACARBOXYLIC ACID COMPOUND, POLYIMIDE THEREOF, AND PRODUCTION METHOD THEREOF MITSUBISHI CHEMICAL CORPORATION (JP) 2009-07-16 US disclosed
US-20050233149-A1 Curable compositions ANSELL CHRISTOPHER 2005-10-20 US disclosed
EP-0885405-B1 PHOTORESIST COMPOSITIONS COMPRISING POLYCYCLIC POLYMERS WITH ACID LABILE PENDANT GROUPS SUMITOMO BAKELITE CO (JP) 2005-06-08 EP disclosed
EP-1056538-B1 ACID ACTIVATION OF RUTHENIUM METATHESIS CATALYSTS AND LIVING ROMP METATHESIS POLYMERIZATION IN WATER CALIFORNIA INST OF TECHN (US) 2005-04-20 EP disclosed
CN-1198181-C Photoresist compositions comprising polycyclic polymers with acid labile pendant groups SUMITOMO BAKELITE CO (JP) 2005-04-20 CN disclosed
US-6790579-B1 PHOTOACID INITIATOR GENERATES ACID EFFECTING POLARITY CHANGE RENDERING POLYMER WATER SOLUBLE IN AREAS EXPOSED TO IMAGING SOURCE; INTEGRATED CIRCUITS, SEMICONDUCTORS SUMITOMO BAKELITE CO., LTD. (JP) 2004-09-14 US disclosed
US-20040151902-A1 Curable compositions ANSELL CHRISTOPHER (GB) 2004-08-05 US disclosed
US-6723486-B2 POLYMERIZING AT LEAST TWO TYPES OF POLYCYCLIC (NORBORNENE) MONOMERS ONE OF WHICH CONTAINING A PENDANT ACID LABILE GROUP AND ANOTHER OF WHICH CONTAINING A PENDNT POLAR FUNCTIONAL GROUP USING A GROUP 8 TRANSITION METAL CATALYST SUMITOMO BAKELITE CO., LTD. (JP) 2004-04-20 US disclosed
EP-1056538-A4 ACID ACTIVATION OF RUTHENIUM METATHESIS CATALYSTS AND LIVING ROMP METATHESIS POLYMERIZATION IN WATER CALIFORNIA INST OF TECHN (US) 2002-12-04 EP disclosed
EP-0544843-A1 HINDERED PHENOLIC NORBORNENE DICARBOXIMIDE MONSANTO COMPANY (US) 1993-06-09 EP disclosed
WO-1992003418-A1 HINDERED PHENOLIC NORBORNENE DICARBOXIMIDE MONSANTO COMPANY (US) 1992-03-05 WO disclosed
US-4647585-A Bicycloheptane substituted ethers E. R. SQUIBB & SONS, INC. (US) 1987-03-03 US disclosed
US-4542160-A Method of use of bicycloheptane substituted prostaglandin analogs as cardiovascular agents E. R. SQUIBB & SONS, INC. (US) 1985-09-17 US disclosed
US-4126738-A Copolymers of 5-norbornene 2,3-dicarboxylic anhydride and maleic anhydride BORG-WARNER CORPORATION (US) 1978-11-21 US disclosed
US-4018767-A 5-ENDO-(1-NAPHTHOYLOXY)-N-(AMINOALKYL) BICYCLO(2.2.1)HEPTANE-2,3-DI-ENDO-CARBOXYLIC ACID IMIDES BRISTOL-MYERS COMPANY (US) 1977-04-19 US disclosed
US-4012575-A Homopolymers of cis-5-norbornene-2,3-dicarboxylic anhydrides BORG-WARNER CORPORATION (US) 1977-03-15 US disclosed
US-3995099-A Copolymers of endo and exo cis-5-norbornene-2,3-dicarboxylic anhydrides LINDAU CHEMICALS, INC., A CORP. OF SC 1976-11-30 US disclosed
US-3980668-A Anti-arrhythimic 5-endo-(3-indolecarbonyloxy)-N-[amino-(lower)alkyl]bicyclo[2,2,1]heptane-2,3-di-endo-carboxylic acid imides BRISTOL-MYERS COMPANY (US) 1976-09-14 US disclosed
US-3936449-A 5-ENDO-CARBAMOYLOXY-N-(AMINO(LOWER)-ALKYL)BICYCLO(2.2.1)HEPTANE-2,3 -DI-ENDO-CARBOXYLIC ACID IMIDES Ohki, Sadao (JA) 1976-02-03 US 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 (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-20090182114-A1 TETRACARBOXYLIC ACID COMPOUND, POLYIMIDE THEREOF, AND PRODUCTION METHOD THEREOF CA1, TTC14, F12 POLB 3322/4885ALDH1A1 2803/4885SMN1; SMN2 3938/4885

“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.