Gemcabene

Gemcabene

SCHEMBL528317

CC(C)(CCCCOCCCCC(C)(C)C(=O)[O-])C(=O)[O-].[Ca+2]

nearest known ligand 0.36

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Known targets — ChEMBL curated mechanism

GABBR1GABBR2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BHMGCRMMP1MMP13MMP7MMP8PTGS1PTGS2ileSpolrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Gemcabene. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
CYP4F2 P78329 2/20 0.36
CYP4A11 Q02928 2/20 0.36
ACLY P53396 1/20 0.35
ACACB O00763 1/20 0.34
ACACA Q13085 1/20 0.34
CES2 O00748 2/20 0.33
FFAR1 O14842 1/20 0.31
CPT2 P23786 1/20 0.31
TDP1 Q9NUW8 1/20 0.31
PPARA Q07869 1/20 0.31
LTB4R Q15722 3/20 0.31
MEN1 O00255 1/20 0.30
THRB P10828 1/20 0.30
HTT P42858 1/20 0.30
KMT2A Q03164 1/20 0.30
MAPT P10636 1/20 0.30
HRH3 Q9Y5N1 1/20 0.30

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
Gemcabene SCHEMBL28467433 0.92 ACLY (0.47) CYP4F2CYP4A11ACLYACACBACACA
SCHEMBL1082921 0.81 ACLY (0.38) CYP4F2CYP4A11ACLYACACBACACA
Gemcabene SCHEMBL761631 0.80 ACLY (0.55) CYP4F2CYP4A11ACLYACACBACACA
SCHEMBL28394389 0.79 ACLY (0.37) CYP4F2CYP4A11ACLYACACBACACA
SCHEMBL4459363 0.79 ACLY (0.37) CYP4F2CYP4A11ACLYACACBACACA
SCHEMBL27363932 0.79 ACLY (0.37) CYP4F2CYP4A11ACLYACACBACACA
SCHEMBL2988405 0.78 CYP4F2 (0.36) CYP4F2CYP4A11ACLYACACBACACA
SCHEMBL5531453 0.78 ACLY (0.59) CYP4F2CYP4A11ACLYACACBACACA
SCHEMBL6258161 0.78 ACLY (0.53) CYP4F2CYP4A11ACLYACACBACACA
Gemcabene SCHEMBL4184554 0.78 ACLY (0.53) CYP4F2CYP4A11ACLYACACBACACA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230248678-A1 GEMCABENE FOR TREATING INFLAMMATION NEUROBO PHARMACEUTICALS, INC. 2023-08-10 US claimed
EP-1715891-B2 METHODS OF TREATING OSTEOARTHRITIS WITH ANTI-IL-6 ANTIBODIES WARNER LAMBERT CO (US) 2014-08-13 EP claimed
US-20100215654-A1 Methods of treating Osteoarthritis with IL-6 Antagonists PFIZER, INC. (US) 2010-08-26 US claimed
EP-1715891-B1 METHODS OF TREATING OSTEOARTHRITIS WITH ANTI-IL-6 ANTIBODIES WARNER LAMBERT CO (US) 2010-04-21 EP claimed
US-20080145367-A1 Methods of Treating Osteoarthritis with Il-6 Antagonists WARNER-LAMBERT COMPAY, LLC 2008-06-19 US claimed
US-20070203212-A1 METHOD OF TREATING OSTEOARTHRITIS WARNER-LAMBERT COMPANY (US) 2007-08-30 US claimed
EP-1715891-A2 METHODS OF TREATING OSTEOARTHRITIS WITH ANTI-IL-6 OR ANTI-IL6 RECEPTOR ANTIBODIES Warner-Lambert Company LLC (US) 2006-11-02 EP claimed
WO-2005080429-A2 METHODS OF TREATING OSTEOARTHRITIS WITH ANTI-IL-6 OR ANTI-IL6 RECEPTOR ANTIBODIES WARNER-LAMBERT COMPANY LLC (US) 2005-09-01 WO claimed
US-20050148654-A1 Statin-carboxyalkylether combinations BISGAIER CHARLES L (US) 2005-07-07 US claimed
EP-1539127-A1 METHOD OF TREATING OSTEOARTHRITIS WARNER-LAMBERT COMPANY LLC (US) 2005-06-15 EP claimed
EP-1280522-B1 COMBINATION OF CARBOXYALKYLETHERS WITH ANTIHYPERTENSIVES AND PHARMACEUTICAL USE WARNER LAMBERT CO (US) 2004-12-01 EP claimed
US-20040072903-A1 Carboxyalkylether-acat inhibitors combinations AUERBACH BRUCE JEFFREY (US) 2004-04-15 US claimed
US-20040048910-A1 Dialkyl ether di-substituted with formyl, carboxy acid, ester and/or tetrazole, which are on tertiary carbon atoms, e.g., 6-(5-carboxy-5-methylhexyloxy)-2,2-dimethylhexanoic acid; lupus, connective tissue disease, sepsis, joint pain WARNER-LAMBERT COMPANY 2004-03-11 US claimed
WO-2004017952-A1 METHOD OF TREATING OSTEOARTHRITIS WARNER-LAMBERT COMPANY LLC (US) 2004-03-04 WO claimed
EP-1292363-A2 CARBOXYALKYLETHER-ACAT INHIBITOR COMBINATIONS WARNER-LAMBERT COMPANY (US) 2003-03-19 EP claimed
WO-2001093845-A2 CARBOXYALKYLETHER-ACAT INHIBITOR COMBINATIONS WARNER-LAMBERT COMPANY (US) 2001-12-13 WO claimed
CN-116710439-B Substituted pyrazolopiperidine carboxylic acids BAYER AG (DE) 2026-05-26 CN disclosed
CN-116829545-B Substituted pyrazolylpiperidine carboxylic acids 拜耳公司 2026-05-15 CN disclosed
US-20040167229-A1 Method of lowering CRP and reducing systemic inflammation BAKKER-ARKEMA REBECCA (US) 2004-08-26 US disclosed
WO-2004045596-A1 METHOD OF LOWERING CRP AND REDUCING SYSTEMIC INFLAMMATION WARNER-LAMBERT COMPANY LLC (US) 2004-06-03 WO 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 (6 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-20040048910-A1 Dialkyl ether di-substituted with formyl, carboxy acid, ester and/or tetrazole, which are on tertiary carbon atoms, e.g., 6-(5-carboxy-5-methylhexyloxy)-2,2-dimethylhexanoic acid; lupus, connective tissue disease, sepsis, joint pain TLR5, SSB, TLR4 CYP4F2 1467/4885CYP4A11 3892/4885ACLY 3034/4885
US-20070203212-A1 METHOD OF TREATING OSTEOARTHRITIS SYVN1, MMP13, TNF CYP4F2 3452/4885CYP4A11 1902/4885ACLY 560/4885
US-20230248678-A1 GEMCABENE FOR TREATING INFLAMMATION CXCL8, IFNG, IL1B CYP4F2 4793/4885CYP4A11 3071/4885ACLY 3052/4885
US-20050148654-A1 Statin-carboxyalkylether combinations HMGCR, CETP, LCAT CYP4F2 300/4885CYP4A11 167/4885ACLY 436/4885
US-20040072903-A1 Carboxyalkylether-acat inhibitors combinations LCAT, CETP, ACAT2 CYP4F2 1292/4885CYP4A11 462/4885ACLY 98/4885
US-20040167229-A1 Method of lowering CRP and reducing systemic inflammation ALB, TTR, IL6 CYP4F2 535/4885CYP4A11 325/4885ACLY 2661/4885

“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.