SCHEMBL6180446

SCHEMBL6180446

[CH2]C(CCCCCCC)C(C)C

nearest known ligand 0.46

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
OPRM1 P35372 1/20 0.46
SPHK1 Q9NYA1 1/20 0.43
LMNA P02545 1/20 0.42
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
ACE2 Q9BYF1 1/20 0.39
GPR84 Q9NQS5 3/20 0.38
FDPS P14324 3/20 0.38
FFAR1 O14842 1/20 0.38
CA1 P00915 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
SCHEMBL28161566 1.00 OPRM1 (0.46) OPRM1SPHK1LMNATSHRTHRB
SCHEMBL28277590 1.00 OPRM1 (0.46) OPRM1SPHK1LMNATSHRTHRB
SCHEMBL9208085 1.00 OPRM1 (0.46) OPRM1SPHK1LMNATSHRTHRB
SCHEMBL28154761 1.00 OPRM1 (0.46) OPRM1SPHK1LMNATSHRTHRB
SCHEMBL11718763 1.00 OPRM1 (0.46) OPRM1SPHK1LMNATSHRTHRB
SCHEMBL28153717 1.00 OPRM1 (0.46) OPRM1SPHK1LMNATSHRTHRB
SCHEMBL28154764 1.00 OPRM1 (0.46) OPRM1SPHK1LMNATSHRTHRB
SCHEMBL21052334 1.00 OPRM1 (0.46) OPRM1SPHK1LMNATSHRTHRB
SCHEMBL21052487 1.00 OPRM1 (0.46) OPRM1SPHK1LMNATSHRTHRB
SCHEMBL1524958 0.97 OPRM1 (0.48) OPRM1SPHK1LMNATSHRTHRB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2019110355-A1 BRANCHED ADIPIC ACID BASED ESTERS AS NOVEL BASE STOCKS AND LUBRICANTS BASF SE (DE) 2019-06-13 WO claimed
CN-106893581-B Organic electroluminescent compounds, organic electroluminescence device and its application 南京高光半导体材料有限公司 2019-11-05 CN disclosed
WO-2019110355-A1 BRANCHED ADIPIC ACID BASED ESTERS AS NOVEL BASE STOCKS AND LUBRICANTS BASF SE (DE) 2019-06-13 WO disclosed
CN-106892915-B Organic compound, organic electroluminescence device and its application 南京高光半导体材料有限公司 2019-02-22 CN disclosed
CN-106892914-B Organic electroluminescent compounds, organic electroluminescence device and its application 南京高光半导体材料有限公司 2019-02-01 CN disclosed
CN-108101922-A Organic electroluminescent compounds, organic electroluminescence device and its application 南京高光半导体材料有限公司 2018-06-01 CN disclosed
CN-106892915-A Organic compound, organic electroluminescence device and its application 南京高光半导体材料有限公司 2017-06-27 CN disclosed
CN-106892914-A Organic electroluminescent compounds, organic electroluminescence device and its application 南京高光半导体材料有限公司 2017-06-27 CN disclosed
CN-106893581-A Organic electroluminescent compounds, organic electroluminescence device and its application 南京高光半导体材料有限公司 2017-06-27 CN disclosed
CN-106866498-A Organic compound, organic electroluminescence device and its application 南京高光半导体材料有限公司 2017-06-20 CN disclosed
US-6924276-B2 Diacid-substituted heteroaryl derivatives as matrix metalloproteinase inhibitors WARNER-LAMBERT COMPANY (US) 2005-08-02 US disclosed
US-20040039208-A1 Process for making n-aryl-anthranilic acids and their derivatives CHEN MICHAEL HUAI GU (US) 2004-02-26 US disclosed
CN-1458921-A Process for making N-aryl-anthranilic acid and their derivatives WARNER LAMBERT CO (US) 2003-11-26 CN disclosed
US-20030099632-A1 Method for preparing a purified matrix metalloproteinase MUELLER WILLIAM THOMAS (US) 2003-05-29 US disclosed
EP-1313694-A1 PROCESS FOR MAKING N-ARYL-ANTHRANILIC ACIDS AND THEIR DERIVATIVES WARNER-LAMBERT COMPANY (US) 2003-05-28 EP disclosed
US-20030087924-A1 Diacid-substituted heteroaryl derivatives as matrix metalloproteinase inhibitors SORENSON RODERICK JOSEPH (US) 2003-05-08 US disclosed
WO-2003033018-A1 METHOD FOR PREPARING PURIFIED MATRIX METALLOPROTEINASE WARNER-LAMBERT COMPANY LLC (US) 2003-04-24 WO disclosed
EP-1304373-A2 Method for preparing a purified matrix metalloproteinase WARNER-LAMBERT COMPANY (US) 2003-04-23 EP disclosed
EP-1291345-A1 Diacid-substituted heteroaryl derivatives as matrix metalloproteinase inhibitors WARNER-LAMBERT COMPANY (US) 2003-03-12 EP disclosed
WO-2002018319-A1 PROCESS FOR MAKING N-ARYL-ANTHRANILIC ACIDS AND THEIR DERIVATIVES WARNER-LAMBERT COMPANY LLC (US) 2002-03-07 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 (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-20040039208-A1 Process for making n-aryl-anthranilic acids and their derivatives AADAC, AHR, AADAT OPRM1 4353/4885SPHK1 4468/4885LMNA 767/4885
US-20030099632-A1 Method for preparing a purified matrix metalloproteinase MMP3, MMP25, MMP7 OPRM1 1816/4885SPHK1 3320/4885LMNA 799/4885
US-20030087924-A1 Diacid-substituted heteroaryl derivatives as matrix metalloproteinase inhibitors MMP13, MMP3, MMP9 OPRM1 2610/4885SPHK1 2383/4885LMNA 2506/4885

“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.