SCHEMBL1008067

SCHEMBL1008067

O=C(O)CCCCCCCOCc1ccccc1

nearest known ligand 0.59

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ MAPT P10636 1/20 0.59
▸ RXFP1 Q9HBX9 1/20 0.59
▸ EPHX2 P34913 2/20 0.57
▸ HDAC3 O15379 2/20 0.53
▸ HDAC4 P56524 2/20 0.53
▸ HDAC1 Q13547 2/20 0.53
▸ HDAC7 Q8WUI4 2/20 0.53
▸ HDAC2 Q92769 2/20 0.53
▸ HDAC10 Q969S8 2/20 0.53
▸ HDAC11 Q96DB2 2/20 0.53
▸ HDAC8 Q9BY41 2/20 0.53
▸ HDAC6 Q9UBN7 2/20 0.53
▸ HDAC9 Q9UKV0 2/20 0.53
▸ HDAC5 Q9UQL6 2/20 0.53
▸ MAPK1 P28482 1/20 0.53
▸ ADRA1A P35348 1/20 0.53
▸ SLC6A3 Q01959 1/20 0.53
▸ SMN1; SMN2 Q16637 1/20 0.53
▸ HTT P42858 1/20 0.51
▸ L3MBTL1 Q9Y468 2/20 0.50

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
SCHEMBL1007119 1.00 MAPT (0.59) MAPTRXFP1EPHX2HDAC3HDAC4
SCHEMBL8984382 1.00 MAPT (0.59) MAPTRXFP1EPHX2HDAC3HDAC4
SCHEMBL6422109 1.00 MAPT (0.59) MAPTRXFP1EPHX2HDAC3HDAC4
SCHEMBL2871485 1.00 MAPT (0.59) MAPTRXFP1EPHX2HDAC3HDAC4
SCHEMBL8984468 1.00 MAPT (0.59) MAPTRXFP1EPHX2HDAC3HDAC4
SCHEMBL2867823 1.00 MAPT (0.59) MAPTRXFP1EPHX2HDAC3HDAC4
SCHEMBL5508985 1.00 MAPT (0.59) MAPTRXFP1EPHX2HDAC3HDAC4
SCHEMBL830483 1.00 MAPT (0.59) MAPTRXFP1EPHX2HDAC3HDAC4
SCHEMBL712393 0.98 MAPT (0.56) MAPTRXFP1EPHX2HDAC3HDAC4
SCHEMBL31482293 0.97 MAPT (0.56) MAPTRXFP1EPHX2HDAC3HDAC4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2025134071-A1 MALIC AND GLUTARIC ACID BASED IONIZABLE LIPIDS SANOFI (FR) 2025-06-26 — — WO disclosed
US-11420933-B2 Lipids and lipid compositions for the delivery of active agents NOVARTIS AG (CH) 2022-08-23 — — US disclosed
EP-3623361-B1 LIPIDS AND LIPID COMPOSITIONS FOR THE DELIVERY OF ACTIVE AGENTS NOVARTIS AG (CH) 2021-08-18 — — EP disclosed
EP-3623361-B1 LIPIDS AND LIPID COMPOSITIONS FOR THE DELIVERY OF ACTIVE AGENTS NOVARTIS AG (CH) 2021-08-18 — — EP disclosed
US-20210078936-A1 LIPIDS AND LIPID COMPOSITIONS FOR THE DELIVERY OF ACTIVE AGENTS NOVARTIS AG (CH) 2021-03-18 — — US disclosed
US-20210078936-A1 LIPIDS AND LIPID COMPOSITIONS FOR THE DELIVERY OF ACTIVE AGENTS NOVARTIS AG (CH) 2021-03-18 — — US disclosed
US-10906867-B2 Lipids and lipid compositions for the delivery of active agents NOVARTIS AG (CH) 2021-02-02 — — US disclosed
US-10906867-B2 Lipids and lipid compositions for the delivery of active agents NOVARTIS AG (CH) 2021-02-02 — — US disclosed
EP-3623361-A1 LIPIDS AND LIPID COMPOSITIONS FOR THE DELIVERY OF ACTIVE AGENTS Novartis AG (CH) 2020-03-18 — — EP disclosed
EP-3083556-B1 LIPIDS AND LIPID COMPOSITIONS FOR THE DELIVERY OF ACTIVE AGENTS NOVARTIS AG (CH) 2019-12-25 — — EP disclosed
US-20090270505-A1 4-DIMETHYLAMINOBUTYRIC ACID DERIVATIVES HOFFMANN-LA ROCHE, INC. 2009-10-29 — — US disclosed
EP-0872467-B1 Process for the production of chiral unsaturated alcohols in high optical purity EASTMAN CHEM CO (US) 2003-01-22 — — EP disclosed
US-6048989-A PARASITICIDES AND ANTIBROTOZOA AGENTS WASHINGTON UNIVERSITY (US) 2000-04-11 — — US disclosed
US-6025511-A A MYRISTIC ACID SELECTED ANALOGS FOR INHIBITING THE BIOSYNTHESIS OF THE GLYCOSYL PHOSPHATIDYLINOSITOL (GPI) ANCHOR OF THE PARASITE WASHINGTON UNIVERSITY (US) 2000-02-15 — — US disclosed
US-6001869-A CONTACTING THE PARASITE WITH 2-THIENYL-UNDECENOIC ACID/10-/ WASHINGTON UNIVERSITY (US) 1999-12-14 — — US disclosed
US-5998642-A Thienyl-containing fatty acid glycosyl phosphatidylinosital analogues used for inhibiting parasitic activity WASHINGTON UNIVERSITY (US) 1999-12-07 — — US disclosed
US-5886214-A CATALYTIC ASYMMETRIC HYDROGENATION OF ENOL ESTERS BEARING A VINYLLIC OR AN ACETYLENIC SUBSTITUENT BY USING A CHIRAL RHODIUM(I) HYDROGENATION CATALYST PREPARED FROM A SUITABLE RHODIUM SALT AND AN OPTICALLY PURE PHOSPHINE LIGAND EASTMAN CHEMICAL COMPANY (US) 1999-03-23 — — US disclosed
EP-0872467-A1 Process for the production of chiral unsaturated alcohols in high optical purity EASTMAN CHEMICAL COMPANY (US) 1998-10-21 — — EP disclosed
US-5760259-A MYRISTIC ACID DERIVATIVES CAPABLE OF INHIBITING BIOSYNTHESIS OF PARASITE'S ANCHORING GROUP WASHINGTON UNIVERSITY (US) 1998-06-02 — — US disclosed
US-5747537-A Method of inhibiting parasitic activity WASHINGTON UNIVERSITY (US) 1998-05-05 — — 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 (4 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-20090270505-A1 4-DIMETHYLAMINOBUTYRIC ACID DERIVATIVES CPT1B, CPT1A, CPT2 MAPT 935/4885RXFP1 2945/4885EPHX2 2708/4885
US-20210078936-A1 LIPIDS AND LIPID COMPOSITIONS FOR THE DELIVERY OF ACTIVE AGENTS LPAR1, LPAR4, LIPA MAPT 3628/4885RXFP1 280/4885EPHX2 1165/4885
US-11420933-B2 Lipids and lipid compositions for the delivery of active agents LPAR1, LPAR4, LIPA MAPT 3628/4885RXFP1 280/4885EPHX2 1165/4885
US-10906867-B2 Lipids and lipid compositions for the delivery of active agents LPAR1, LPAR4, LIPA MAPT 3628/4885RXFP1 280/4885EPHX2 1165/4885

“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.

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