SCHEMBL381033

SCHEMBL381033

CC(C)(O)CCCCC(=O)O

nearest known ligand 0.55

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 2/20 0.55
TSHR P16473 5/20 0.52
NFKB1 P19838 1/20 0.52
PMP22 Q01453 1/20 0.52
AKR1B1 P15121 1/20 0.50
GPR84 Q9NQS5 8/20 0.48
PPARG P37231 7/20 0.48
PPARD Q03181 7/20 0.48
PPARA Q07869 7/20 0.48
HDAC11 Q96DB2 5/20 0.48
PTPN1 P18031 3/20 0.48
TDP1 Q9NUW8 3/20 0.48
ALDH1A1 P00352 2/20 0.48
TLR2 O60603 2/20 0.48
FABP4 P15090 2/20 0.48
SLC22A6 Q4U2R8 2/20 0.48
FFAR1 O14842 2/20 0.48
SLC22A8 Q8TCC7 1/20 0.48
MEN1 O00255 1/20 0.48
ESR1 P03372 1/20 0.48

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
SCHEMBL11216421 0.98 TSHR (0.57) LMNATSHRNFKB1PMP22AKR1B1
SCHEMBL9794217 0.98 TSHR (0.57) LMNATSHRNFKB1PMP22AKR1B1
SCHEMBL380537 0.98 TSHR (0.57) LMNATSHRNFKB1PMP22AKR1B1
SCHEMBL381203 0.92 LMNA (0.50) LMNATSHRNFKB1PMP22AKR1B1
SCHEMBL18879234 0.91 LMNA (0.46) LMNATSHRNFKB1PMP22AKR1B1
Adipic Acid SCHEMBL27574535 0.86 GPR84 (0.52) LMNATSHRNFKB1PMP22AKR1B1
SCHEMBL28631627 0.84 CAMK2A (0.48) LMNATSHRNFKB1PMP22AKR1B1
SCHEMBL29114063 0.82 MAPT (0.45) LMNATSHRNFKB1PMP22AKR1B1
Butyric Acid SCHEMBL9343652 0.82 FFAR3 (0.54) TSHRAKR1B1GPR84PPARGPPARD
SCHEMBL1908887 0.82 LMNA (0.58) LMNATSHRNFKB1PMP22AKR1B1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3793973-B1 PROCESS FOR PRODUCING AN INTRAMOLECULAR DIESTER OF A HYDROXYCARBOXYLIC ACID AND PROCESS FOR PRODUCING A POLYHYDROXYCARBOXYLIC ACID. FRAUNHOFER GES FORSCHUNG (DE) 2022-12-28 EP claimed
EP-3793973-A1 PROCESS FOR PRODUCING AN INTRAMOLECULAR DIESTER OF A HYDROXYCARBOXYLIC ACID AND PROCESS FOR PRODUCING A POLYHYDROXYCARBOXYLIC ACID. FRAUNHOFER-GESELLSCHAFT zur Förderung der angewandten Forschung e.V. (DE) 2021-03-24 EP claimed
WO-2009127009-A1 CONDENSATION POLYMERS COMMONWEALTH SCIENTIFIC AND INDUSTRIAL RESEARCH ORGANISATION (AU) 2009-10-22 WO claimed
US-4945180-A Process for the preparation of E-2-propyl-2-pentenoic acid and physiologically compatible salts thereof DESITIN ARZNEIMITTEL GMBH (DE) 1990-07-31 US claimed
EP-3793973-B1 PROCESS FOR PRODUCING AN INTRAMOLECULAR DIESTER OF A HYDROXYCARBOXYLIC ACID AND PROCESS FOR PRODUCING A POLYHYDROXYCARBOXYLIC ACID. FRAUNHOFER GES FORSCHUNG (DE) 2022-12-28 EP disclosed
US-20210139390-A1 PRODUCTION METHOD OF ORGANIC COMPOUND UNITIKA LTD. (JP) 2021-05-13 US disclosed
EP-3819283-A1 METHOD FOR PRODUCING ORGANIC COMPOUND Unitika Ltd. (JP) 2021-05-12 EP disclosed
EP-3793973-A1 PROCESS FOR PRODUCING AN INTRAMOLECULAR DIESTER OF A HYDROXYCARBOXYLIC ACID AND PROCESS FOR PRODUCING A POLYHYDROXYCARBOXYLIC ACID. FRAUNHOFER-GESELLSCHAFT zur Förderung der angewandten Forschung e.V. (DE) 2021-03-24 EP disclosed
CN-112384489-A Method for producing organic compound 尤尼吉可株式会社 2021-02-19 CN disclosed
US-10752690-B2 Biologically active molecule conjugates, reagents and methods of manufacture, and therapeutic uses REGENERON PHARMACEUTICALS, INC. (US) 2020-08-25 US disclosed
US-20180312597-A1 Biologically active molecule conjugates, reagents and methods of manufacture, and therapeutic uses REGENERON PHARMACEUTICALS, INC. 2018-11-01 US disclosed
EP-2460848-B1 FILLER FOR USE IN RUBBER AND RUBBER COMPOSITION OSAKA SODA CO LTD (JP) 2018-09-05 EP disclosed
US-5512653-A Lactic acid containing hydroxycarboxylic acid for the preparation of polhydroxycarboxylic acid MITSUI TOATSU CHEMICALS, INC. (JP) 1996-04-30 US disclosed
EP-0707024-A2 Purification process of polyhydroxycarboxylic acids MITSUI TOATSU CHEMICALS, Inc. (JP) 1996-04-17 EP disclosed
US-5444143-A Preparation process of polyhydroxycarboxylic acid MITSUI TOATSU CHEMICALS, INC. (JP) 1995-08-22 US disclosed
US-5440008-A Condensation polymerization of hydroxycarboxylic acids in vertical reactor with ribbon stirrer, having flow pattern along walls in opposite direction to flow along axis of stirrer MITSUI TOATSU CHEMICALS, INC. (JP) 1995-08-08 US disclosed
US-5386004-A Contacting with acid substance in presence of organic solvent MITSUI TOATSU CHEMICALS, INC. (JP) 1995-01-31 US disclosed
EP-0603889-A2 Process for the preparation of lactic acid polyesters MITSUI TOATSU CHEMICALS, Inc. (JP) 1994-06-29 EP disclosed
EP-0591978-A2 Polyhydroxycarboxylic acid and purification process thereof MITSUI TOATSU CHEMICALS, Inc. (JP) 1994-04-13 EP disclosed
US-4945180-A Process for the preparation of E-2-propyl-2-pentenoic acid and physiologically compatible salts thereof DESITIN ARZNEIMITTEL GMBH (DE) 1990-07-31 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 (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-20180312597-A1 Biologically active molecule conjugates, reagents and methods of manufacture, and therapeutic uses CD22, CD2, CD47 LMNA 3679/4885TSHR 2388/4885NFKB1 1791/4885
US-10752690-B2 Biologically active molecule conjugates, reagents and methods of manufacture, and therapeutic uses CD22, CD2, CD47 LMNA 3679/4885TSHR 2388/4885NFKB1 1791/4885

“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.