SCHEMBL441909

SCHEMBL441909

[CH]=CCCC1CCCCC1

nearest known ligand 0.46

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
▸ CYP1A2 P05177 1/20 0.42
▸ SIGMAR1 Q99720 3/20 0.39
▸ ADH1B P00325 1/20 0.34
▸ ADH1C P00326 1/20 0.34
▸ ADH1A P07327 1/20 0.34
▸ ADH4 P08319 1/20 0.34
▸ ADH7 P40394 1/20 0.34
▸ HPGD P15428 1/20 0.33
▸ METAP1 P53582 1/20 0.32
▸ CHRM5 P08912 2/20 0.32
▸ ADRA2C P18825 1/20 0.32
▸ CHRM2 P08172 1/20 0.32
▸ CHRM4 P08173 1/20 0.32
▸ CHRM1 P11229 1/20 0.32
▸ EPHX1 P07099 1/20 0.31
▸ NFE2L2 Q16236 1/20 0.31
▸ POLB P06746 1/20 0.31
▸ GAA P10253 1/20 0.31

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
SCHEMBL2240667 0.97 — —
SCHEMBL962972 0.92 — —
SCHEMBL542372 0.86 — —
SCHEMBL6589344 0.85 CYP1A2 (0.50) CYP1A2SIGMAR1ADH1BADH1CADH1A
SCHEMBL450392 0.85 CYP1A2 (0.50) CYP1A2SIGMAR1ADH1BADH1CADH1A
SCHEMBL452274 0.83 SIGMAR1 (0.50) CYP1A2SIGMAR1CHRM5ADRA2CEPHX1
SCHEMBL7403531 0.83 SIGMAR1 (0.50) CYP1A2SIGMAR1CHRM5ADRA2CEPHX1
SCHEMBL6033221 0.82 CYP1A2 (0.46) CYP1A2SIGMAR1CHRM5ADRA2CEPHX1
SCHEMBL6877800 0.78 CYP1A2 (0.46) CYP1A2SIGMAR1ADH1BADH1CADH1A
SCHEMBL6593058 0.77 — —

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1599464-B1 NOVEL CYCLIC UREA DERIVATIVES, PREPARATION METHOD THEREOF AND PHARMACEUTICAL USE OF SAME AS KINASE INHIBITORS AVENTIS PHARMA SA (FR) 2010-09-22 — — EP claimed
US-20070249710-A1 Biaromatic compounds and cosmetic/pharmaceutical applications thereof GALDERMA RESEARCH & DEVELOPMENT (FR) 2007-10-25 — — US claimed
US-20240199623-A1 SUBSTITUTED PYRAZOLO[1,5-a]PYRIMIDINES AS CFTR MODULATORS ILDONG PHARMACEUTICAL CO., LTD. (KR) 2024-06-20 — — US disclosed
US-20240166593-A1 LIPIDS SUITABLE FOR NUCLEIC ACID DELIVERY RAMOT AT TEL-AVIV UNIVERSITY LTD. (IL) 2024-05-23 — — US disclosed
EP-4370106-A1 CANNABIDIOLIC ACID ESTERS FOR TREATING PRADER-WILLI SYNDROME EPM (IP), Inc. (US) 2024-05-22 — — EP disclosed
US-11970493-B2 Autotaxin inhibitor compounds ILDONG PHARMACEUTICAL CO., LTD. (KR) 2024-04-30 — — US disclosed
CN-117813081-A Cannabidiol esters for the treatment of Prader-Willi syndrome EPM(IP)公司 2024-04-02 — — CN disclosed
WO-2024003906-A1 CANNABINOID DERIVATIVES AND COMPOSITIONS COMPRISING SAME CANNASOUL ANALYTICS LTD. (IL) 2024-01-04 — — WO disclosed
US-11851389-B2 Cationic lipids for nucleic acid delivery and preparation thereof RAMOT AT TEL-AVIV UNIVERSITY LTD. (IL) 2023-12-26 — — US disclosed
WO-2023244059-A1 METHODS OF TREATING CANCER USING DUAL ANDROGEN RECEPTOR AND PDE5 INHIBITOR COMPOUNDS ILDONG PHARMACEUTICAL CO., LTD. (KR) 2023-12-21 — — WO disclosed
EP-4288104-A1 LIPIDS SUITABLE FOR NUCLEIC ACID DELIVERY Ramot at Tel-Aviv University Ltd. (IL) 2023-12-13 — — EP disclosed
WO-1998054158-A1 QUINOLINE AND QUINOXALINE COMPOUNDS WHICH INHIBIT PLATELET-DERIVED GROWTH FACTOR AND/OR p56lck TYROSINE KINASES RHÔNE-POULENC RORER PHARMACEUTICALS INC. (US) 1998-12-03 — — WO disclosed
WO-1998054157-A1 QUINOLINE AND QUINOXALINE COMPOUNDS WHICH INHIBIT PLATELET-DERIVED GROWTH FACTOR AND/OR p561ck TYROSINE KINASES RHÔNE-POULENC RORER PHARMACEUTICALS INC. (US) 1998-12-03 — — WO disclosed
WO-1998051324-A1 PEPTIDE PARATHYROID HORMONE ANALOGS RHONE-POULENC RORER PHARMACEUTICALS INC. (US) 1998-11-19 — — WO disclosed
EP-0871439-A1 SUBSTITUTED (ARYL, HETEROARYL, ARYLMETHYL OR HETEROARYLMETHYL) HYDROXAMIC ACID COMPOUNDS RHONE-POULENC RORER PHARMACEUTICALS, INC. (US) 1998-10-21 — — EP disclosed
WO-1998032734-A1 SUBSTITUTED β-THIOCARBOXYLIC ACIDS RHONE-POULENC RORER PHARMACEUTICALS INC. (US) 1998-07-30 — — WO disclosed
WO-1998029376-A1 PROCESS FOR THE SOLID PHASE SYNTHESIS OF ALDEHYDES, KETONES, OXIMES, AMINES AND HYDROXAMIC ACID COMPOUNDS RHONE-POULENC RORER PHARMACEUTICALS INC. (US) 1998-07-09 — — WO disclosed
US-5750540-A SIDE EFFECT REDUCTION BANYU PHARMACEUTICAL CO., LTD. (JP) 1998-05-12 — — US disclosed
EP-0823423-A1 1,4-DISUBSTITUTED PIPERIDINE DERIVATIVES BANYU PHARMACEUTICAL CO., LTD. (JP) 1998-02-11 — — EP disclosed
WO-1997024117-A1 SUBSTITUTED (ARYL, HETEROARYL, ARYLMETHYL OR HETEROARYLMETHYL) HYDROXAMIC ACID COMPOUNDS RHONE-POULENC RORER PHARMACEUTICALS INC. (US) 1997-07-10 — — 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 (5 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-11851389-B2 Cationic lipids for nucleic acid delivery and preparation thereof NPC1L1, NPC1, CETP CYP1A2 4711/4885SIGMAR1 2111/4885ADH1B 2789/4885
US-20240199623-A1 SUBSTITUTED PYRAZOLO[1,5-a]PYRIMIDINES AS CFTR MODULATORS PDE4A, PDE4B, PDE6C CYP1A2 2115/4885SIGMAR1 3875/4885ADH1B 1270/4885
US-20240166593-A1 LIPIDS SUITABLE FOR NUCLEIC ACID DELIVERY NPC1L1, NPC1, FASN CYP1A2 4572/4885SIGMAR1 2483/4885ADH1B 1694/4885
US-11970493-B2 Autotaxin inhibitor compounds ENPP2, ATXN10, ATXN2L CYP1A2 4674/4885SIGMAR1 4497/4885ADH1B 4688/4885
US-20070249710-A1 Biaromatic compounds and cosmetic/pharmaceutical applications thereof RARG, RARA, RARB CYP1A2 463/4885SIGMAR1 3668/4885ADH1B 135/4885

“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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