SCHEMBL4274565

SCHEMBL4274565

CCCCCCCCC(C)CC(C)C

nearest known ligand 0.48

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
ACE2 Q9BYF1 1/20 0.48
OPRM1 P35372 1/20 0.46
LMNA P02545 2/20 0.43
SPHK1 Q9NYA1 1/20 0.43
TSHR P16473 1/20 0.42
THRB P10828 1/20 0.42
DNM1 Q05193 2/20 0.42
ADH1B P00325 1/20 0.40
ADH1C P00326 1/20 0.40
ADH1A P07327 1/20 0.40
ADH4 P08319 1/20 0.40
ADH7 P40394 1/20 0.40
GPR84 Q9NQS5 3/20 0.38
FDPS P14324 3/20 0.38
FFAR1 O14842 1/20 0.38

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
SCHEMBL27196676 1.00 ACE2 (0.48) ACE2OPRM1LMNASPHK1TSHR
SCHEMBL4271879 1.00 ACE2 (0.48) ACE2OPRM1LMNASPHK1TSHR
SCHEMBL671349 1.00 ACE2 (0.48) ACE2OPRM1LMNASPHK1TSHR
SCHEMBL27223056 1.00 ACE2 (0.48) ACE2OPRM1LMNASPHK1TSHR
SCHEMBL1873151 0.97 OPRM1 (0.48) ACE2OPRM1LMNASPHK1TSHR
SCHEMBL1645053 0.95 ACE2 (0.45) ACE2OPRM1LMNASPHK1TSHR
SCHEMBL27223874 0.95 ACE2 (0.45) ACE2OPRM1LMNASPHK1TSHR
SCHEMBL27470379 0.95 ACE2 (0.45) ACE2OPRM1LMNASPHK1TSHR
SCHEMBL27345411 0.92 OPRM1 (0.44) ACE2OPRM1LMNASPHK1TSHR
SCHEMBL27753327 0.92 LMNA (0.55) ACE2OPRM1LMNASPHK1TSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119207584-A Computer-implemented method for evaluating plant nitrogen absorption capacity through rhizosphere soil environmental characteristics 贵州省蚕业研究所(贵州省辣椒研究所) 2024-12-27 CN claimed
CN-122030497-A Fermentation method for cooperatively treating ganoderma lucidum by bacterial enzymes and application of fermentation method in pet food 杭州半边野兽科技有限公司 2026-05-15 CN disclosed
EP-4583719-A1 COMPOSITIONS AND METHODS FOR PRODUCING AROMAS Nourish Ingredients Pty Ltd (AU) 2025-07-16 EP disclosed
US-20250197341-A1 METHOD FOR INHIBITING CRYSTALLISATION BIOSYNTHIS (FR) 2025-06-19 US disclosed
CN-119207584-A Computer-implemented method for evaluating plant nitrogen absorption capacity through rhizosphere soil environmental characteristics 贵州省蚕业研究所(贵州省辣椒研究所) 2024-12-27 CN disclosed
EP-4387582-A1 METHOD FOR INHIBITING CRYSTALLISATION Biosynthis (FR) 2024-06-26 EP disclosed
CN-117940101-A Method for inhibiting crystallization 碧昂赛恩斯公司 2024-04-26 CN disclosed
US-20240084343-A1 METHODS OF USING NATURAL AND ENGINEERED ORGANISMS TO PRODUCE SMALL MOLECULES FOR INDUSTRIAL APPLICATION KIVERDI INC (US) 2024-03-14 US disclosed
WO-2024050588-A1 COMPOSITIONS AND METHODS FOR PRODUCING AROMAS Nourish Ingredients Pty Ltd (AU) 2024-03-14 WO disclosed
WO-2023020979-A1 METHOD FOR INHIBITING CRYSTALLISATION BIOSYNTHIS (FR) 2023-02-23 WO disclosed
US-20140273112-A1 METHODS OF USING NATURAL AND ENGINEERED ORGANISMS TO PRODUCE SMALL MOLECULES FOR INDUSTRIAL APPLICATION KIVERDI, INC. (US) 2014-09-18 US disclosed
EP-2718395-A1 NOVEL COLOR CONVERTER BASF SE (DE) 2014-04-16 EP disclosed
US-20130109893-A1 FUEL COMPOSITIONS CONTAINING AN ISOMERIZED COMPONENT OF A SINGLE CARBON NUMBER AND METHODS OF PREPARING THE FUEL COMPOSITIONS UNIVERSITY OF DAYTON (US) 2013-05-02 US disclosed
WO-2012168395-A1 NOVEL COLOR CONVERTER BASF SE (DE) 2012-12-13 WO disclosed
WO-2009037283-A1 METHOD FOR PRODUCING SUBSTRATES COATED WITH RYLENE TETRACARBOLIC ACID DIIMIDES BASF SE (DE) 2009-03-26 WO disclosed
US-20090078312-A1 VERFAHREN ZUR HERSTELLUNG VON MIT RYLENTETRACARBONSAEUREDIIMIDEN BESCHICHTETEN SUBSTRATEN BASF SE (DE) 2009-03-26 US disclosed
EP-0656569-A1 Liquid electrostatic developers with reduced dispersant emissions E.I. DU PONT DE NEMOURS AND COMPANY (US) 1995-06-07 EP disclosed
EP-0421441-B1 Pantothenic acid derivatives FUJIREBIO KK (JP) 1995-01-25 EP disclosed
US-5120738-A Cardiovascular disorders FUJIREBIO INC. (JP) 1992-06-09 US disclosed
EP-0421441-A2 Pantothenic acid derivatives FUJIREBIO INC. (JP) 1991-04-10 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-20250197341-A1 METHOD FOR INHIBITING CRYSTALLISATION FASN, SCD5, NFKB2 ACE2 449/4885OPRM1 4200/4885LMNA 149/4885
US-20090078312-A1 VERFAHREN ZUR HERSTELLUNG VON MIT RYLENTETRACARBONSAEUREDIIMIDEN BESCHICHTETEN SUBSTRATEN AXIN2, NCSTN, NES ACE2 601/4885OPRM1 4144/4885LMNA 2799/4885

“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.