SCHEMBL5439892

SCHEMBL5439892

O=C=NC1CCCC2CCCCC21

nearest known ligand 0.43

Predicted protein targets (top 1)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 1/20 0.43

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
SCHEMBL4048773 0.96 ALDH1A1 (0.48) ALDH1A1
SCHEMBL20932711 0.89 ALDH1A1 (0.48) ALDH1A1
SCHEMBL1231779 0.86 ALDH1A1 (0.44) ALDH1A1
Methane SCHEMBL11125010 0.84 ALDH1A1 (0.52) ALDH1A1
SCHEMBL8729993 0.81 ALDH1A1 (0.50) ALDH1A1
SCHEMBL26012 0.78 ALDH1A1 (0.57) ALDH1A1
SCHEMBL26610 0.78 ALDH1A1 (0.50) ALDH1A1
SCHEMBL5460574 0.78 ALDH1A1 (0.57) ALDH1A1
SCHEMBL9323923 0.78 ALDH1A1 (0.57) ALDH1A1
SCHEMBL11492208 0.77 APLNR (0.39)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2949676-B1 NON-HOT-MELT MDI-BASED POLYURETHANE COMPOSITION BEARING NCO END GROUPS AND HAVING A LOW CONTENT OF MDI MONOMER, COMPRISING AT LEAST ONE ISOCYANATE COMPOUND OF PARTICULAR MOLAR VOLUME BOSTIK SA (FR) 2023-02-22 EP disclosed
US-11078322-B2 Non-hot-melt MDI-based polyurethane composition bearing NCO end groups and having a low content of MDI monomer, comprising at least one isocyanate compound of particular molar volume BOSTIK SA (FR) 2021-08-03 US disclosed
US-20190309122-A1 NON-HOT-MELT MDI-BASED POLYURETHANE COMPOSITION BEARING NCO END GROUPS AND HAVING A LOW CONTENT OF MDI MONOMER, COMPRISING AT LEAST ONE ISOCYANATE COMPOUND OF PARTICULAR MOLAR VOLUME BOSTIK SA (FR) 2019-10-10 US disclosed
US-10370481-B2 Non-hot-melt 2,4-TDI-based polyurethane composition bearing NCO end groups and having a low content of TDI monomer, comprising at least one isocyanate compound of particular molar volume BOSTIK SA (FR) 2019-08-06 US disclosed
US-10358523-B2 Non-hot-melt MDI-based polyurethane composition bearing NCO end groups and having a low content of MDI monomer, comprising at least one isocyanate compound of particular molar volume BOSTIK SA (FR) 2019-07-23 US disclosed
CN-103476803-B Celluosic resin and manufacture method thereof NEC CORP. (JP) 2016-03-16 CN disclosed
US-20150344612-A1 NON-HOT-MELT 2,4-TDI-BASED POLYURETHANE COMPOSITION BEARING NCO END GROUPS AND HAVING A LOW CONTENT OF TDI MONOMER, COMPRISING AT LEAST ONE ISOCYANATE COMPOUND OF PARTICULAR MOLAR VOLUME BOSTIK SA (FR) 2015-12-03 US disclosed
US-20150344612-A1 NON-HOT-MELT 2,4-TDI-BASED POLYURETHANE COMPOSITION BEARING NCO END GROUPS AND HAVING A LOW CONTENT OF TDI MONOMER, COMPRISING AT LEAST ONE ISOCYANATE COMPOUND OF PARTICULAR MOLAR VOLUME BOSTIK SA (FR) 2015-12-03 US disclosed
US-20150344614-A1 Non-hot-melt MDI-based polyurethane composition bearing NCO end groups and having a low content of MDI monomer, comprising at least one isocyanate compound of particular molar volume BOSTIK SA (FR) 2015-12-03 US disclosed
US-20150344614-A1 Non-hot-melt MDI-based polyurethane composition bearing NCO end groups and having a low content of MDI monomer, comprising at least one isocyanate compound of particular molar volume BOSTIK SA (FR) 2015-12-03 US disclosed
EP-2949676-A1 NON-HOT-MELT MDI-BASED POLYURETHANE COMPOSITION BEARING NCO END GROUPS AND HAVING A LOW CONTENT OF MDI MONOMER, COMPRISING AT LEAST ONE ISOCYANATE COMPOUND OF PARTICULAR MOLAR VOLUME BOSTIK SA (FR) 2015-12-02 EP disclosed
EP-2949677-A1 NON-HOT-MELT 2,4-TDI-BASED POLYURETHANE COMPOSITION BEARING NCO END GROUPS AND HAVING A LOW CONTENT OF TDI MONOMER, COMPRISING AT LEAST ONE ISOCYANATE COMPOUND OF PARTICULAR MOLAR VOLUME BOSTIK SA (FR) 2015-12-02 EP disclosed
CN-103476803-A Cellulose resin and method for producing same NEC CORP 2013-12-25 CN disclosed
US-20070282078-A1 Synthesis of aryl N-acylurea from aryl isocyanates or aryl carbodiimides for use as intermediate in novel sequential self-repetitive reaction (SSRR) to form amides, amide-imides and their polymers NATIONAL CHUNG HSING UNIVERSITY (TW) 2007-12-06 US disclosed
US-4096334-A Process for the manufacture of carbodiimides HOECHST AKTIENGESELLSCHAFT (DT) 1978-06-20 US disclosed
US-4066629-A PROCESS FOR PREPARING CARBODIIMIDES UTILIZING A PHOSPHONIUM SALT CATALYST CELANESE CORPORATION (US) 1978-01-03 US disclosed
US-3960950-A Process for carbodiiomide synthesis MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1976-06-01 US disclosed