SCHEMBL130404

SCHEMBL130404

N[C@@H](CC(=O)O)C(=O)O[SiH3]

nearest known ligand 0.39

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ SMN1; SMN2 Q16637 1/20 0.39
▸ SLC22A6 Q4U2R8 1/20 0.36
▸ GABRR1 P24046 2/20 0.36
▸ LMNA P02545 1/20 0.36
▸ TDP1 Q9NUW8 1/20 0.35
▸ GRIK1 P39086 2/20 0.34
▸ GRIK2 Q13002 2/20 0.34
▸ GRM1 Q13255 2/20 0.34
▸ GRM2 Q14416 2/20 0.34
▸ GRM8 O00222 1/20 0.34
▸ GRM6 O15303 1/20 0.34
▸ GRIN2D O15399 1/20 0.34
▸ GRIN3B O60391 1/20 0.34
▸ GSR P00390 1/20 0.34
▸ CYP1A2 P05177 1/20 0.34
▸ GRM5 P41594 1/20 0.34
▸ GRIA1 P42261 1/20 0.34
▸ GRIA2 P42262 1/20 0.34
▸ GRIA3 P42263 1/20 0.34
▸ SLC1A3 P43003 1/20 0.34

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
SCHEMBL7972219 0.81 ALOX15 (0.33) —
SCHEMBL1653844 0.80 SLC22A6 (0.39) SMN1; SMN2SLC22A6GABRR1LMNATDP1
SCHEMBL30338047 0.78 SLC22A6 (0.38) SMN1; SMN2SLC22A6GABRR1LMNATDP1
SCHEMBL28753674 0.78 SLC22A6 (0.38) SMN1; SMN2SLC22A6GABRR1LMNATDP1
SCHEMBL62914 0.78 SLC22A6 (0.38) SMN1; SMN2SLC22A6GABRR1LMNATDP1
SCHEMBL25491154 0.78 SLC22A6 (0.38) SMN1; SMN2SLC22A6GABRR1LMNATDP1
SCHEMBL3831500 0.78 SLC22A6 (0.38) SMN1; SMN2SLC22A6GABRR1LMNATDP1
SCHEMBL28002998 0.78 SLC22A6 (0.38) SMN1; SMN2SLC22A6GABRR1LMNATDP1
Hydrochloric Acid SCHEMBL11804611 0.78 SLC22A6 (0.38) SMN1; SMN2SLC22A6GABRR1LMNATDP1
Hydrochloric Acid SCHEMBL25204383 0.76 SLC22A6 (0.36) SMN1; SMN2SLC22A6GABRR1LMNATDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20200347183-A1 SILANE-MODIFIED POLYUREA COMPOUNDS BASED ON POLYISOCYANATES HAVING ISOCYANURATE AND ALLOPHANATE GROUPS COVESTRO DEUTSCHLAND AG (DE) 2020-11-05 — — US disclosed
EP-3732225-A1 SILANE-MODIFIED POLYUREA COMPOUNDS BASED ON POLYISOCYANATES HAVING ISOCYANURATE AND ALLOPHANATE GROUPS Covestro Deutschland AG (DE) 2020-11-04 — — EP disclosed
EP-1346001-B1 TWO-COMPONENT COATING COMPOSITIONS CONTAINING SILANE ADHESION PROMOTERS BAYER CORP (US) 2012-08-08 — — EP disclosed
EP-1578830-B1 MOISTURE-CURABLE, POLYETHER URETHANES WITH TERMINAL CYCLIC UREA/REACTIVE SILANE GROUPS AND THEIR USE AS SEALANTS, ADHESIVES AND COATINGS BAYER MATERIALSCIENCE LLC (US) 2012-04-04 — — EP disclosed
EP-1578829-B1 A PROCESS FOR THE PREPARATION OF MOISTURE-CURABLE, POLYETHER URETHANES WITH TERMINAL CYCLIC UREA/REACTIVE SILANE GROUPS BAYER MATERIALSCIENCE LLC (US) 2012-03-07 — — EP disclosed
EP-1678225-B1 MOISTURE-CURABLE, POLYETHER URETHANES WITH REACTIVE SILANE GROUPS AND THEIR USE AS SEALANTS, ADHESIVES AND COATINGS BAYER MATERIALSCIENCE LLC (US) 2011-11-23 — — EP disclosed
EP-1685171-B1 MOISTURE-CURABLE, POLYETHER URETHANES WITH REACTIVE SILANE GROUPS AND THEIR USE AS SEALANTS, ADHESIVES AND COATINGS BAYER MATERIALSCIENCE LLC (US) 2008-03-12 — — EP disclosed
US-7309753-B2 Process for the preparation of moisture-curable, polyether urethanes with terminal cyclic urea reactive silane groups BAYER MATERIALSCIENCE LLC (US) 2007-12-18 — — US disclosed
CN-1930201-A Moisture-curable polyether urethanes with reactive silane groups and their use as sealants, adhesives and coatings BAYER MATERIALSCIENCE LLC (US) 2007-03-14 — — CN disclosed
CN-1871271-A Moisture-curable, polyether urethanes with reactive silane groups and their use as sealants, adhesives and coatings BAYER MATERIALSCIENCE LLC (US) 2006-11-29 — — CN disclosed
US-20030232942-A1 Polyether urethanes containing one reactive silane group and their use in moisture-curable polyether urethanes BAYER POLYMERS LLC 2003-12-18 — — US disclosed
US-20030232950-A1 MOISTURE-CURABLE, POLYETHER URETHANES WITH REACTIVE SILANE GROUPS AND THEIR USE AS SEALANTS, ADHESIVES AND COATINGS BAYER POLYMERS LLC 2003-12-18 — — US disclosed
US-20030232949-A1 MOISTURE-CURABLE, POLYETHER URETHANES WITH REACTIVE SILANE GROUPS AND THEIR USE AS SEALANTS, ADHESIVES AND COATINGS BAYER POLYMERS LLC 2003-12-18 — — US disclosed
US-20030229192-A1 Moisture-curable, polyether urethanes with reactive silane groups and their use as sealants, adhesives and coatings BAYER POLYMERS LLC 2003-12-11 — — US disclosed
US-20030225235-A1 Moisture-curable, polyether urethanes with reactive silane groups and their use as sealants, adhesives and coatings BAYER AKTIENGESELLSCHAFT (DE) 2003-12-04 — — US disclosed
US-20030225237-A1 MOISTURE-CURABLE, POLYETHER URETHANES WITH REACTIVE SILANE GROUPS AND THEIR USE AS SEALANTS, ADHESIVES AND COATINGS BAYER POLYMERS LLC 2003-12-04 — — US disclosed
EP-1346001-A2 TWO-COMPONENT COATING COMPOSITIONS CONTAINING SILANE ADHESION PROMOTERS Bayer Corporation (US) 2003-09-24 — — EP disclosed
US-6444325-B1 POLYURETHANE; PROTECTIVE COATING FOR PIPES BAYER CORPORATION 2002-09-03 — — US disclosed
US-20020119330-A1 Two-component coating compositions containing silane adhesion promoters COVESTRO LLC 2002-08-29 — — US disclosed
WO-2002051954-A2 TWO-COMPONENT COATING COMPOSITIONS CONTAINING SILANE ADHESION PROMOTERS BAYER CORPORATION (US) 2002-07-04 — — WO disclosed
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