SCHEMBL2491946

SCHEMBL2491946

CCCCCC(=O)CC(=O)OCC

nearest known ligand 0.56

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
GAA P10253 2/20 0.56
MGAM O43451 1/20 0.56
SI P14410 1/20 0.56
MGAM2 Q2M2H8 1/20 0.56
HAO1 Q9UJM8 1/20 0.52
FAAH O00519 4/20 0.50
DGKA P23743 1/20 0.50
MAPT P10636 2/20 0.47
KMT2A Q03164 1/20 0.47
PAM P19021 2/20 0.46
CYP1A2 P05177 1/20 0.45
CES2 O00748 4/20 0.44
CES1 P23141 4/20 0.44
AKR1B1 P15121 1/20 0.43
TSHR P16473 1/20 0.43

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
SCHEMBL3171122 0.98 HAO1 (0.55) GAAMGAMSIMGAM2HAO1
SCHEMBL6138462 0.98 HAO1 (0.55) GAAMGAMSIMGAM2HAO1
SCHEMBL6138788 0.98 HAO1 (0.55) GAAMGAMSIMGAM2HAO1
SCHEMBL3777425 0.98 HAO1 (0.55) GAAMGAMSIMGAM2HAO1
SCHEMBL472723 0.98 HAO1 (0.55) GAAMGAMSIMGAM2HAO1
SCHEMBL6138989 0.98 HAO1 (0.55) GAAMGAMSIMGAM2HAO1
SCHEMBL6138705 0.98 HAO1 (0.55) GAAMGAMSIMGAM2HAO1
SCHEMBL6138882 0.98 HAO1 (0.55) GAAMGAMSIMGAM2HAO1
SCHEMBL3442509 0.98 HAO1 (0.55) GAAMGAMSIMGAM2HAO1
SCHEMBL1903946 0.98 HAO1 (0.55) GAAMGAMSIMGAM2HAO1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-102653531-B Synthesis method of massoia lactone SHANGHAI AIPU VEGETABLE TECHNOLOGY CO LTD 2014-08-13 CN claimed
EP-1361801-B1 AUTOINDUCER COMPOUNDS AND THEIR USES PATHWAY INTERMEDIATES LTD (GB) 2007-06-06 EP claimed
US-20040115245-A1 Autoinducer compounds and their uses GORMAR MARKETING LIMITED (KY) 2004-06-17 US claimed
EP-1361801-A1 AUTOINDUCER COMPOUNDS AND THEIR USES Gormar Marketing Limited (KY) 2003-11-19 EP claimed
WO-2002052949-A1 AUTOINDUCER COMPOUNDS AND THEIR USES GORMAR MARKETING LIMITED (KY) 2002-07-11 WO claimed
EP-0912467-B1 ASYMMETRIC HYDROGENATION METHOD OF A KETONIC COMPOUND AND DERIVATIVE RHODIA CHIMIE SA (FR) 2002-04-24 EP claimed
CN-1010689-B AQUEOUS COATING COMPOSITION AND PROCESS OF COATING SUBSTRATE WITH SUCH COATING COMPOSITION AKZO NV (NL) 1990-12-05 CN claimed
CN-87106519-A The method of aqueous coating composition and coated substrates thereof 1988-04-06 CN claimed
US-20250282743-A1 METHODS OF SYNTHESIZING CANNABIDIOL, DERIVATIVES THEREOF, AND OTHER PHYTOCANNABINOIDS CITRACHEM CORP. 2025-09-11 US disclosed
US-20250207159-A1 Microorganisms And Methods For Production Of Fatty Acid Derivatives With Reduced Levels Of Byproducts AGAIN BIO APS (DK) 2025-06-26 US disclosed
EP-4493675-A1 MICROORGANISMS AND METHODS FOR PRODUCTION OF FATTY ACID DERIVATIVES WITH REDUCED LEVELS OF BYPRODUCTS Genomatica, Inc. (US) 2025-01-22 EP disclosed
EP-4469426-A2 METHODS OF SYNTHESIZING CANNABIDIOL, DERIVATIVES THEREOF, AND OTHER PHYTOCANNABINOIDS CitraChem Corp. (US) 2024-12-04 EP disclosed
CN-114901774-B Two-part curable polyurethane adhesive, cured product of two-part curable polyurethane adhesive, and polyurethane adhesive sheet 三洋化成工业株式会社 2023-11-03 CN disclosed
WO-2023178211-A1 MICROORGANISMS AND METHODS FOR PRODUCTION OF FATTY ACID DERIVATIVES WITH REDUCED LEVELS OF BYPRODUCTS GENOMATICA, INC. (US) 2023-09-21 WO disclosed
EP-0128584-A1 Dihydrofuran derivates useful as aroma chemicals, and process for their preparation QUANTUM CHEMICAL CORPORATION (a Virginia corp.) (US) 1984-12-19 EP disclosed
US-4487946-A USING QUATERNARY AMONIUM OR PHOSPHONIUM CATALYST NATIONAL DISTILLERS AND CHEMICAL CORPORATION (US) 1984-12-11 US disclosed
US-4249027-A Process for the preparation of 5-substituted resorcinols and related intermediates CIBA-GEIGY CORPORATION (US) 1981-02-03 US disclosed
US-4109006-A 1,4-DITHIINOXIDES WARREN-TEED LABORATORIES, INC. (US) 1978-08-22 US disclosed
US-4020098-A Process for the preparation of 5-substituted resorcinols and related intermediates CIBA-GEIGY CORPORATION (US) 1977-04-26 US disclosed
US-3980700-A Prostaglandin intermediates and optically active isomers thereof G. D. SEARLE & CO. (US) 1976-09-14 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-20250282743-A1 METHODS OF SYNTHESIZING CANNABIDIOL, DERIVATIVES THEREOF, AND OTHER PHYTOCANNABINOIDS CNR2, CNR1, CYP8B1 GAA 4027/4885MGAM 2188/4885SI 342/4885

“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.