Tolazoline

Tolazoline

SCHEMBL3463645

O=S(=O)(O)S.c1ccc(CC2=NCCN2)cc1

nearest known ligand 0.76

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CHRH1HRH2

The experimentally established mechanism targets of Tolazoline. 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
ADRA2A known ✓ P08913 3/20 0.76
ADRA2C known ✓ P18825 3/20 0.76
ADRA1A known ✓ P35348 3/20 0.76
ADRA2B known ✓ P18089 2/20 0.76
ADRA1D known ✓ P25100 2/20 0.76
ADRA1B known ✓ P35368 2/20 0.76
HRH1 known ✓ P35367 1/20 0.49
TAAR1 Q96RJ0 5/20 0.76
CYP2D6 P10635 3/20 0.76
LMNA P02545 2/20 0.76
CYP1A2 P05177 2/20 0.76
TSHR P16473 2/20 0.76
RAD52 P43351 1/20 0.65
HTR1B P28222 4/20 0.56
NISCH Q9Y2I1 3/20 0.55
MAOA P21397 2/20 0.55
MAOB P27338 2/20 0.55
HTR1D P28221 5/20 0.54
NFKB1 P19838 1/20 0.52
KDM4E B2RXH2 1/20 0.49

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
Tolazoline SCHEMBL3463648 0.91 TAAR1 (0.76) TAAR1CYP2D6ADRA2AADRA2CADRA1A
Tolazoline SCHEMBL34961 0.87 TAAR1 (1.00) TAAR1CYP2D6ADRA2AADRA2CADRA1A
Tolazoline SCHEMBL28254903 0.85 TAAR1 (0.96) TAAR1CYP2D6ADRA2AADRA2CADRA1A
Tolazoline SCHEMBL5053858 0.85 TAAR1 (1.00) TAAR1CYP2D6ADRA2AADRA2CADRA1A
Tolazoline SCHEMBL34869 0.85 TAAR1 (1.00) TAAR1CYP2D6ADRA2AADRA2CADRA1A
Tolazoline SCHEMBL9614505 0.85 TAAR1 (1.00) TAAR1CYP2D6ADRA2AADRA2CADRA1A
Tolazoline SCHEMBL9221347 0.84 TAAR1 (0.81) TAAR1CYP2D6ADRA2AADRA2CADRA1A
Tolazoline SCHEMBL28268861 0.83 TAAR1 (0.78) TAAR1CYP2D6ADRA2AADRA2CADRA1A
Phthalic Acid SCHEMBL28266376 0.82 TAAR1 (0.76) TAAR1CYP2D6ADRA2AADRA2CADRA1A
Tolazoline SCHEMBL27969662 0.81 TAAR1 (0.73) TAAR1CYP2D6ADRA2AADRA2CADRA1A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20080116076-A1 METHOD AND COMPOSITION FOR DIRECT METALLIZATION OF NON-CONDUCTIVE SUBSTRATES ENTHONE INC. (US) 2008-05-22 US claimed
US-8330039-B2 Solar cell modules with poly(vinyl butyral) encapsulant comprising unsaturated heterocyclic compound E I DU PONT DE NEMOURS AND COMPANY (US) 2012-12-11 US disclosed
CN-102292826-A Solar cell modules with poly(vinyl butyral) encapsulant comprising unsaturated heterocyclic compound 2011-12-21 CN disclosed
US-20100180947-A1 SOLAR CELL MODULES WITH POLY(VINYL BUTYRAL) ENCAPSULANT COMPRISING UNSATURATED HETEROCYCLIC COMPOUND E. I. DU PONT DE NEMOURS AND COMPANY (US) 2010-07-22 US disclosed
US-20080116076-A1 METHOD AND COMPOSITION FOR DIRECT METALLIZATION OF NON-CONDUCTIVE SUBSTRATES ENTHONE INC. (US) 2008-05-22 US disclosed
US-20030013830-A1 Reacting a thiosulfate salt with a halogenated styrenic monomer to form a styrenic thiosulfate salt monomer and then polymerization of said monomer in the presence of an initiator BLEVINS RICHARD W (US) 2003-01-16 US disclosed
US-6420505-B1 STYRENE THIOSULFATE AND OLEFIN MONOMER EASTMAN KODAK COMPANY 2002-07-16 US disclosed