SCHEMBL1713038

SCHEMBL1713038

CCCCN(CCCC)C(N(CCCC)CCCC)=[N+](CCCC)CCCC

nearest known ligand 0.41

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
CA12 O43570 4/20 0.41
CA1 P00915 4/20 0.41
CA9 Q16790 4/20 0.41
ALDH1A1 P00352 2/20 0.41
ALDH2 P05091 1/20 0.41
CA2 P00918 2/20 0.39
MMP1 P03956 1/20 0.39
MMP2 P08253 1/20 0.39
MMP3 P08254 1/20 0.39
MMP8 P22894 1/20 0.39
MGLL Q99685 1/20 0.32

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
Hydrochloric Acid SCHEMBL1535756 0.98 CA12 (0.40) CA12CA1CA9ALDH1A1ALDH2
Bromide SCHEMBL6155069 0.98 CA12 (0.40) CA12CA1CA9ALDH1A1ALDH2
Iodide SCHEMBL7030478 0.98 CA12 (0.40) CA12CA1CA9ALDH1A1ALDH2
Fluoride Ion SCHEMBL5446663 0.98 CA12 (0.40) CA12CA1CA9ALDH1A1ALDH2
Hydrochloric Acid SCHEMBL6265698 0.96 CA12 (0.39) CA12CA1CA9ALDH1A1ALDH2
Hydrochloric Acid SCHEMBL25406366 0.94 CA12 (0.38) CA12CA1CA9ALDH1A1ALDH2
SCHEMBL7027230 0.92 CA12 (0.38) CA12CA1CA9ALDH1A1ALDH2
Hydrochloric Acid SCHEMBL14862018 0.92 CA12 (0.44) CA12CA1CA9ALDH1A1ALDH2
Hydrochloric Acid SCHEMBL25405687 0.92 CA12 (0.42) CA12CA1CA9ALDH1A1ALDH2
SCHEMBL7034958 0.90 ALDH1A1 (0.45) CA12CA1CA9ALDH1A1ALDH2

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 18 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1960408-B1 PROCESS FOR THE PRODUCTION OF MERCAPTOALKYLALKOXYSILANES MOMENTIVE PERFORMANCE MAT INC (US) 2011-07-20 EP claimed
WO-2025101604-A1 CATALYST SYSTEM AND USES ULTRACLEAN FUEL PTY LTD (AU) 2025-05-15 WO disclosed
CN-119487001-A 3,3' -Aromatic bis (etherimide), polyetherimide thereof and preparation method thereof 高新特殊工程塑料全球技术有限公司 2025-02-18 CN disclosed
US-20150380168-A1 THIN-LAYER CAPACITORS WITH LARGE SCALE INTEGRATION SIEMENS AKTIENGESELLSCHAFT (DE) 2015-12-31 US disclosed
EP-1922324-B1 PROCESS FOR PRODUCING ORGANOALKOXYSILANES FROM ORGANIC ACIDS OR CYANATES AND HALOALKYLALKOXYSILNANES MOMENTIVE PERFORMANCE MAT INC (US) 2013-07-17 EP disclosed
US-7528273-B2 Aqueous catalytic process for the preparation of thiocarboxylate silane MOMENTIVE PERFORMANCE MATERIALS INC. (US) 2009-05-05 US disclosed
EP-1922324-A1 PROCESS FOR PRODUCING ORGANOALKOXYSILANES FROM ORGANIC ACIDS OR CYANATES AND HALOALKYLALKOXYSILNANES Momentive Performance Materials Inc. (US) 2008-05-21 EP disclosed
US-7262312-B2 Process for producing organoalkoxysilanes from organic acids or cyanates and haloalkylalkoxysilanes MOMENTIVE PERFORMANCE MATERIALS INC. 2007-08-28 US disclosed
WO-2007018997-A1 PROCESS FOR PRODUCING ORGANOALKOXYSILANES FROM ORGANIC ACIDS OR CYANATES AND HALOALKYLALKOXYSILNANES MOMENTIVE PERFORMANCE MATERIALS INC. (US) 2007-02-15 WO disclosed
US-20070032673-A1 PROCESS FOR PRODUCING ORGANOALKOXYSILANES FROM ORGANIC ACIDS OR CYANATES AND HALOALKYLALKOXYSILANES MOMENTIVE PERFORMANCE MATERIALS INC. 2007-02-08 US disclosed
EP-0736490-B1 Layered minerals and compositions comprising the same GEN ELECTRIC (US) 2003-06-04 EP disclosed
EP-1121344-A2 CHEMICAL PROCESSES AVENTIS CROPSCIENCE S.A. (FR) 2001-08-08 EP disclosed
WO-2000021922-A2 CHEMICAL PROCESSES AVENTIS CROPSCIENCE S.A. (FR) 2000-04-20 WO disclosed
US-5905150-A HEATING IN PRESENCE OF PHASE TRANSFER AGENT GENERAL ELECTRIC COMPANY (US) 1999-05-18 US disclosed
EP-0900801-A1 Process for preparing organosilanes GENERAL ELECTRIC COMPANY (US) 1999-03-10 EP disclosed
EP-0736490-A1 Layered minerals and compositions comprising the same GENERAL ELECTRIC COMPANY (US) 1996-10-09 EP disclosed
US-5530052-A SILICATE MINERALS THAT HAVE UNDERGONE A CATION EXCHANGE WITH A POSITIVELY CHARGED ORGANO-SUBSTITUTED HETEROATOM GENERAL ELECTRIC COMPANY (US) 1996-06-25 US disclosed
US-5283358-A Using an aromatic ether and acyl halide; in presence of hexaalkylguanidinium or tetraalkylphosphonium salt catalyst SOCIETE NATIONALE DES POUDRES ET EXPLOSIFS (FR) 1994-02-01 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 (1 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-20070032673-A1 PROCESS FOR PRODUCING ORGANOALKOXYSILANES FROM ORGANIC ACIDS OR CYANATES AND HALOALKYLALKOXYSILANES OGA, ALKBH3, SLC43A1 CA12 146/4885CA1 344/4885CA9 35/4885

“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.