SCHEMBL97795

SCHEMBL97795

OCCCCCOCc1ccccc1

nearest known ligand 0.54

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
L3MBTL1 Q9Y468 2/20 0.54
TDP1 Q9NUW8 1/20 0.54
TSHR P16473 1/20 0.54
UGCG Q16739 5/20 0.50
GBA2 Q9HCG7 5/20 0.50
GBA1 P04062 4/20 0.50
EPHX2 P34913 3/20 0.47
LTA4H P09960 1/20 0.47
KDM4E B2RXH2 1/20 0.46
POLB P06746 1/20 0.46
HRH4 Q9H3N8 1/20 0.45
HRH3 Q9Y5N1 1/20 0.45
ADRB2 P07550 1/20 0.43
ADRB1 P08588 1/20 0.43
ADRB3 P13945 1/20 0.43
LCT P09848 2/20 0.43
SI P14410 2/20 0.43
MGAM O43451 1/20 0.43
TEAD3 Q99594 1/20 0.42
NAAA Q02083 1/20 0.42

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
SCHEMBL518615 1.00 L3MBTL1 (0.54) L3MBTL1TDP1TSHRUGCGGBA2
SCHEMBL1246210 1.00 L3MBTL1 (0.54) L3MBTL1TDP1TSHRUGCGGBA2
SCHEMBL8482826 1.00 L3MBTL1 (0.54) L3MBTL1TDP1TSHRUGCGGBA2
SCHEMBL6212152 1.00 L3MBTL1 (0.54) L3MBTL1TDP1TSHRUGCGGBA2
SCHEMBL96809 1.00 L3MBTL1 (0.54) L3MBTL1TDP1TSHRUGCGGBA2
SCHEMBL9684333 1.00 L3MBTL1 (0.54) L3MBTL1TDP1TSHRUGCGGBA2
SCHEMBL25208054 1.00 L3MBTL1 (0.54) L3MBTL1TDP1TSHRUGCGGBA2
SCHEMBL814418 1.00 L3MBTL1 (0.54) L3MBTL1TDP1TSHRUGCGGBA2
SCHEMBL1007794 1.00 L3MBTL1 (0.54) L3MBTL1TDP1TSHRUGCGGBA2
SCHEMBL22906771 0.98 L3MBTL1 (0.53) L3MBTL1TDP1TSHRUGCGGBA2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115028680-B PROTAC compound for targeted degradation of Cyclophilin A and preparation method and application thereof 深圳湾实验室 2023-01-20 CN claimed
CN-115028680-A PROTAC compound for targeted degradation of Cyclophilin A and preparation method and application thereof 深圳湾实验室 2022-09-09 CN claimed
US-6989052-B1 Phase change ink printing process XEROX CORPORATION (US) 2006-01-24 US claimed
US-20060004123-A1 PHASE CHANGE INK PRINTING PROCESS XEROX CORPORATION 2006-01-05 US claimed
EP-4743465-A1 BICYCLIC MACROCYCLES FOR THE TREATMENT OF AUTOIMMUNE DISEASE F. Hoffmann-La Roche AG (CH) 2026-05-20 EP disclosed
US-12594339-B2 Lipid prodrugs of JAK inhibitors and uses thereof SEAPORT THERAPEUTICS, INC. (US) 2026-04-07 US disclosed
EP-4712974-A2 STAT DEGRADERS AND USES THEREOF Recludix Pharma, Inc. (US) 2026-03-25 EP disclosed
EP-4709370-A2 STAT DEGRADERS AND USES THEREOF Recludix Pharma, Inc. (US) 2026-03-18 EP disclosed
US-12569464-B2 Protein-protein interaction inducing technology ARVINAS OPERATIONS, INC. (US) 2026-03-10 US disclosed
US-12559486-B2 Tau-protein targeting compounds and associated methods of use ARVINAS OPERATIONS, INC. (US) 2026-02-24 US disclosed
EP-3681875-B1 CYCLIC PEPTIDE ANTIBIOTICS HOFFMANN LA ROCHE (CH) 2026-01-14 EP disclosed
US-12448323-B2 Dental glass composition KURARAY NORITAKE DENTAL INC. (JP) 2025-10-21 US disclosed
US-5488140-A ANTICONVULSANTS CIBA-GEIGY CORPORATION (US) 1996-01-30 US disclosed
US-5294734-A 1-phosphato-4-amino-pent-2-enoic acids and derivatives CIBA-GEIGY CORP. (US) 1994-03-15 US disclosed
US-5155113-A Administering 5-fluorouracil and derivatives with pyridine and pyridone derivatives OTSUKA PHARMACEUTICAL CO., LTD. (JP) 1992-10-13 US disclosed
US-5145865-A Fatty acid, cholesterol synthesis inhibitors; enzyme inhibitors; antilipemic agents OTSUKA PHARMACEUTICAL COMPANY, LIMITED (JP) 1992-09-08 US disclosed
EP-0180188-B1 A COMPOSITION FOR INCREASING THE ANTI-CANCER ACTIVITY OF AN ANTI-CANCER COMPOUND OTSUKA PHARMACEUTICAL CO., LTD. (JP) 1992-04-15 EP disclosed
US-5081287-A Pesticidal polyhalo alkenoic acid esters FMC CORPORATION (US) 1992-01-14 US disclosed
EP-0393607-A2 Phenylcarboxylic acid derivatives having a hetero ring OTSUKA PHARMACEUTICAL CO., LTD. (JP) 1990-10-24 EP disclosed
EP-0180188-A2 A composition for increasing the anti-cancer activity of an anti-cancer compound OTSUKA PHARMACEUTICAL CO., LTD. (JP) 1986-05-07 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 (3 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-12569464-B2 Protein-protein interaction inducing technology STUB1, MDM2, XIAP L3MBTL1 198/4885TDP1 2247/4885TSHR 2796/4885
US-12559486-B2 Tau-protein targeting compounds and associated methods of use UBQLN2, UBQLN1, CRBN L3MBTL1 539/4885TDP1 1778/4885TSHR 2915/4885
US-12594339-B2 Lipid prodrugs of JAK inhibitors and uses thereof JAK1, JAK3, JAK2 L3MBTL1 2032/4885TDP1 1878/4885TSHR 432/4885

“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.