SCHEMBL13585915

SCHEMBL13585915

CCCCCCCCC1(CCCCCCCC)c2cc(C)ccc2-c2ccc(-c3ccc(-c4ccc(-c5ccc(C)s5)c5nsnc45)s3)cc21

nearest known ligand 0.00

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

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
SCHEMBL11977576 1.00 — —
SCHEMBL14570397 1.00 — —
SCHEMBL12621077 1.00 — —
SCHEMBL29433154 1.00 — —
SCHEMBL12611469 1.00 — —
SCHEMBL14850155 0.93 — —
SCHEMBL11994082 0.91 CNR1 (0.33) —
SCHEMBL12983006 0.91 CNR1 (0.33) —
SCHEMBL12982382 0.91 CNR1 (0.33) —
SCHEMBL14217362 0.91 CNR1 (0.33) —

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20190234953-A1 FUNCTIONALIZED CHROMOPHORIC POLYMER DOTS AND BIOCONJUGATES THEREOF CLEMSON UNIVERSITY 2019-08-01 — — US disclosed
EP-3483610-A1 FUNCTIONALIZED CHROMOPHORIC POLYMER DOTS AND BIOCONJUGATES THEREOF University Of Washington Center For Commercialization (US) 2019-05-15 — — EP disclosed
US-10191060-B2 Functionalized chromophoric polymer dots and bioconjugates thereof UNIVERSITY OF WASHINGTON (US) 2019-01-29 — — US disclosed
EP-2499213-B1 FUNCTIONALIZED CHROMOPHORIC POLYMER DOTS AND BIOCONJUGATES THEREOF UNIV OF WASHINGTON CENTER FOR COMMERCIALIZATION (US) 2019-01-16 — — EP disclosed
US-9834640-B2 Nanoparticles CHROMITION LIMITED (GB) 2017-12-05 — — US disclosed
US-20160329498-A1 FULLERENE DERIVATIVES AND ORGANIC ELECTRONIC DEVICE COMPRISING FULLERENE DERIVATIVES LG CHEM, LTD. (KR) 2016-11-10 — — US disclosed
US-20160237205-A1 NANOPARTICLES THE UNIVERSITY OF MANCHESTER (GB) 2016-08-18 — — US disclosed
US-20160013392-A1 METHOD OF PRODUCING THERMOELECTRIC CONVERSION ELEMENT AND METHOD OF PREPARATION DISPERSION FOR THERMOELECTRIC CONVERSION LAYER FUJIFILM CORPORATION (JP) 2016-01-14 — — US disclosed
US-20150221885-A1 PHOTOELECTRIC CONVERSION DEVICE AND FABRICATION METHOD THEREFOR FUJITSU LIMITED (JP) 2015-08-06 — — US disclosed
US-20140318625-A1 CONDUCTIVE POLYMER COMPRISING 3,6-CARBAZOLE AND ORGANIC SOLAR CELL USING SAME LG CHEM, LTD. (KR) 2014-10-30 — — US disclosed
US-20140251407-A1 THERMOELECTRIC CONVERSION MATERIAL AND A THERMOELECTRIC CONVERSION ELEMENT FUJIFILM CORPORATION (JP) 2014-09-11 — — US disclosed
US-20140230871-A1 THERMOELECTRIC CONVERSION MATERIAL AND THERMOELECTRIC CONVERSION ELEMENT FUJIFILM CORPORATION (JP) 2014-08-21 — — US disclosed
US-20120282632-A1 FUNCTIONALIZED CHROMOPHORIC POLYMER DOTS AND BIOCONJUGATES THEREOF CLEMSON UNIVERSITY (US) 2012-11-08 — — US disclosed
US-20090048413-A1 Method for Production of Conjugated Polymer SUMITOMO CHEMICAL COMPANY, LIMITED 2009-02-19 — — US disclosed
Send feedback