SCHEMBL597672

SCHEMBL597672

O=S(=O)(O)c1ccccc1.O=S(=O)(O)c1ccccc1.O=S(=O)(O)c1ccccc1.O=S(=O)(O)c1ccccc1.O=S(=O)(O)c1ccccc1.O=S(=O)(O)c1ccccc1.[Na]

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Known targets — ChEMBL curated mechanism

BTKCACNA1CCACNA1DCACNA1FCACNA1SCACNA2D1CACNA2D2DRD2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQHRH1HTR2AP2RY12

The experimentally established mechanism targets of None. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 3/20 1.00
SMN1; SMN2 Q16637 1/20 1.00
POLB P06746 1/20 0.62
CYP2D6 P10635 1/20 0.62
HTR6 P50406 1/20 0.58
LMNA P02545 1/20 0.57
ALDH1A1 P00352 4/20 0.55
NT5E P21589 1/20 0.55
TDP1 Q9NUW8 3/20 0.52
CA1 P00915 2/20 0.52
CA2 P00918 2/20 0.52
HSD17B10 Q99714 2/20 0.52
CA12 O43570 1/20 0.52
CA3 P07451 1/20 0.52
CA4 P22748 1/20 0.52
CA6 P23280 1/20 0.52
CA5A P35218 1/20 0.52
CA7 P43166 1/20 0.52
PLA2G7 Q13093 1/20 0.52
CA9 Q16790 1/20 0.52

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
SCHEMBL3409457 1.00 TSHR (1.00) TSHRSMN1; SMN2POLBCYP2D6HTR6
Benzene SCHEMBL9751882 1.00 TSHR (1.00) TSHRSMN1; SMN2POLBCYP2D6HTR6
SCHEMBL1079321 1.00 TSHR (1.00) TSHRSMN1; SMN2POLBCYP2D6HTR6
SCHEMBL30307036 1.00 TSHR (1.00) TSHRSMN1; SMN2POLBCYP2D6HTR6
SCHEMBL2509 1.00 TSHR (1.00) TSHRSMN1; SMN2POLBCYP2D6HTR6
SCHEMBL125188 1.00 TSHR (1.00) TSHRSMN1; SMN2POLBCYP2D6HTR6
SCHEMBL30671620 1.00 TSHR (1.00) TSHRSMN1; SMN2POLBCYP2D6HTR6
SCHEMBL30812783 1.00 TSHR (1.00) TSHRSMN1; SMN2POLBCYP2D6HTR6
SCHEMBL9871011 0.97 TSHR (0.94) TSHRSMN1; SMN2POLBCYP2D6HTR6
Hydrochloric Acid SCHEMBL11436653 0.97 TSHR (0.94) TSHRSMN1; SMN2POLBCYP2D6HTR6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8114476-B2 Process for improving the insulating capacity of expanded vinyl aromatic polymers and the products thus obtained POLIMERI EUROPA S.P.A. (IT) 2012-02-14 US disclosed
US-20110020542-A1 PROCESS FOR IMPROVING THE INSULATING CAPACITY OF EXPANDED VINYL AROMATIC POLYMERS AND THE PRODUCTS THUS OBTAINED POLIMERI EUROPA S.P.A. (IT) 2011-01-27 US disclosed
US-7825165-B2 Process or improving the insulating capacity of expanded vinyl aromatic polymers and the products thus obtained POLIMERI EUROPA S.P.A. (IT) 2010-11-02 US disclosed
US-20090068354-A1 Process for Improving the Insulating Capacity of Expanded Vinyl Aromatic Polymers and the Products thus Obtained POLIMERI EUROPA S.P.A. (IT) 2009-03-12 US disclosed
EP-1877473-A2 PROCESS FOR IMPROVING THE INSULATING CAPACITY FOR EXPANDED VINYL AROMATIC POLYMERS AND THE PRODUCTS THUS OBTAINED Polimeri Europa S.p.A. (IT) 2008-01-16 EP disclosed
WO-2006108672-A2 PROCESS FOR IMPROVING THE INSULATING CAPACITY FOR EXPANDED VINYL AROMATIC POLYMERS AND THE PRODUCTS THUS OBTAINED POLIMERI EUROPA S.P.A. (IT) 2006-10-19 WO disclosed