Sugi Predict

Sugi Predict / Compounds / SCHEMBL11997754

SCHEMBL11997754

SCHEMBL11997754

Cc1ccc(-c2ccc(-c3ccc(-c4ccc(-c5ccc(-c6ccc(C)s6)s5)s4)s3)s2)s1

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ NPC1 O15118 5/20 0.50
▸ MAPT P10636 4/20 0.50
▸ ALDH1A1 P00352 2/20 0.50
▸ HSD17B10 Q99714 2/20 0.50
▸ GFER P55789 1/20 0.50
▸ RAB9A P51151 3/20 0.42
▸ KDM4E B2RXH2 3/20 0.42
▸ SMN1; SMN2 Q16637 2/20 0.42
▸ TP53 P04637 1/20 0.42
▸ HPGD P15428 1/20 0.42
▸ NFKB1 P19838 1/20 0.42
▸ NFKB2 Q00653 1/20 0.42
▸ RELA Q04206 1/20 0.42
▸ CHRM2 P08172 1/20 0.42
▸ CHRM4 P08173 1/20 0.42
▸ CHRM5 P08912 1/20 0.42
▸ CHRM1 P11229 1/20 0.42
▸ CHRM3 P20309 1/20 0.42
▸ DAO P14920 1/20 0.40
▸ CASP3 P42574 1/20 0.40

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
SCHEMBL120939 1.00 NPC1 (0.50) NPC1MAPTALDH1A1HSD17B10GFER
SCHEMBL12170048 1.00 NPC1 (0.50) NPC1MAPTALDH1A1HSD17B10GFER
SCHEMBL12982405 1.00 NPC1 (0.50) NPC1MAPTALDH1A1HSD17B10GFER
SCHEMBL12982161 1.00 NPC1 (0.50) NPC1MAPTALDH1A1HSD17B10GFER
SCHEMBL29764 0.97 NPC1 (0.52) NPC1MAPTALDH1A1HSD17B10GFER
SCHEMBL13376691 0.89 APP (0.50) NPC1MAPTALDH1A1HSD17B10GFER
SCHEMBL12887840 0.87 CYP3A4 (0.46) NPC1MAPTALDH1A1HSD17B10GFER
SCHEMBL12982748 0.84 NPC1 (0.41) NPC1MAPTALDH1A1HSD17B10GFER
SCHEMBL8508163 0.84 MAPT (0.42) NPC1MAPTALDH1A1HSD17B10GFER
SCHEMBL13407308 0.84 NPC1 (0.41) NPC1MAPTALDH1A1HSD17B10GFER

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230197491-A1 METHODS AND SYSTEMS HAVING CONDUCTIVE POLYMER COATING FOR ELECTROSTATIC DISCHARGE APPLICATIONS ENTEGRIS, INC. 2023-06-22 — — US disclosed
US-20230197491-A1 METHODS AND SYSTEMS HAVING CONDUCTIVE POLYMER COATING FOR ELECTROSTATIC DISCHARGE APPLICATIONS ENTEGRIS, INC. 2023-06-22 — — US disclosed
EP-2313409-B1 SEMICONDUCTOR MATERIALS AND METHODS OF PREPARATION AND USE THEREOF BASF SE (DE) 2014-11-26 — — EP disclosed
US-8808877-B2 Organic electroluminescent element and method of manufacturing the same SHARP KABUSHIKI KAISHA (JP) 2014-08-19 — — US disclosed
US-8808877-B2 Organic electroluminescent element and method of manufacturing the same SHARP KABUSHIKI KAISHA (JP) 2014-08-19 — — US disclosed
US-8569501-B2 Semiconductor materials and methods of preparation and use thereof BASF SE (DE) 2013-10-29 — — US disclosed
US-8569501-B2 Semiconductor materials and methods of preparation and use thereof BASF SE (DE) 2013-10-29 — — US disclosed
US-8298686-B2 Composition and organic photoelectric converter using the same SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2012-10-30 — — US disclosed
US-20120211702-A1 Electrically Conducting Polymer And Copolymer Compositions, Methods For Making Same And Applications Therefor THE OHIO STATE UNIVERSITY (US) 2012-08-23 — — US disclosed
US-20120211702-A1 Electrically Conducting Polymer And Copolymer Compositions, Methods For Making Same And Applications Therefor THE OHIO STATE UNIVERSITY (US) 2012-08-23 — — US disclosed
US-7842198-B2 n-Type thiophene semiconductors NORTHWESTERN UNIVERSITY (US) 2010-11-30 — — US disclosed
WO-2009144302-A1 SEMICONDUCTOR MATERIALS AND METHODS OF PREPARATION AND USE THEREOF BASF SE (DE) 2009-12-03 — — WO disclosed
US-20090218933-A1 ORGANIC ELECTROLUMINESCENT DEVICE IDEMITSU KOSAN CO., LTD (JP) 2009-09-03 — — US disclosed
US-20090218933-A1 ORGANIC ELECTROLUMINESCENT DEVICE IDEMITSU KOSAN CO., LTD (JP) 2009-09-03 — — US disclosed
US-20080293937-A1 n-Type Thiophene Semiconductors POLYERA CORPORATION 2008-11-27 — — US disclosed
US-7374702-B2 n-Type thiophene semiconductors NORTHWESTERN UNIVERSITY (US) 2008-05-20 — — US disclosed
US-20080100213-A1 LUMINESCENT DEVICE IDEMITSU KOSAN CO., LTD. (JP) 2008-05-01 — — US disclosed
US-20080100213-A1 LUMINESCENT DEVICE IDEMITSU KOSAN CO., LTD. (JP) 2008-05-01 — — US disclosed
US-20070287848-A1 Silicon Compound Containi-Electron Conjugated-System Molecule and Process for Producing the Same SHARP KABUSHIKI KAISHA (JP) 2007-12-13 — — US disclosed
US-20070287848-A1 Silicon Compound Containi-Electron Conjugated-System Molecule and Process for Producing the Same SHARP KABUSHIKI KAISHA (JP) 2007-12-13 — — 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 (2 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-20070287848-A1 Silicon Compound Containi-Electron Conjugated-System Molecule and Process for Producing the Same SEM1, F12, ESPL1 NPC1 2175/4885MAPT 1715/4885ALDH1A1 1828/4885
US-20080293937-A1 n-Type Thiophene Semiconductors FTH1, FECH, CD2 NPC1 1293/4885MAPT 1158/4885ALDH1A1 2700/4885

“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.