SCHEMBL7651554

SCHEMBL7651554

COc1cc(CCl)cc(OC)c1OC(C)=O

nearest known ligand 0.49

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TUBB4A P04350 2/20 0.49
TUBB P07437 2/20 0.49
TUBA3C P0DPH7 2/20 0.49
TUBA1B P68363 2/20 0.49
TUBA4A P68366 2/20 0.49
TUBB4B P68371 2/20 0.49
TUBB3 Q13509 2/20 0.49
TUBB2A Q13885 2/20 0.49
TUBB8 Q3ZCM7 2/20 0.49
TUBA3E Q6PEY2 2/20 0.49
TUBA1A Q71U36 2/20 0.49
TUBA1C Q9BQE3 2/20 0.49
TUBB6 Q9BUF5 2/20 0.49
TUBB2B Q9BVA1 2/20 0.49
TUBB1 Q9H4B7 2/20 0.49
ALOX5 P09917 3/20 0.47
PTGS1 P23219 1/20 0.45
TNFSF11 O14788 1/20 0.44
GRIN2D O15399 1/20 0.44
GRIN3B O60391 1/20 0.44

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
SCHEMBL3391679 0.87 ALOX15 (0.53) TUBB4ATUBBTUBA3CTUBA1BTUBA4A
SCHEMBL7659166 0.84 TUBB4A (0.50) TUBB4ATUBBTUBA3CTUBA1BTUBA4A
SCHEMBL16256702 0.81 MEN1 (0.59) TUBB4ATUBBTUBA3CTUBA1BTUBA4A
SCHEMBL30251689 0.81 TUBB4A (0.48) TUBB4ATUBBTUBA3CTUBA1BTUBA4A
SCHEMBL10926373 0.79 ABCB11 (0.53) TUBB4ATUBBTUBA3CTUBA1BTUBA4A
SCHEMBL8779397 0.79 PTGS1 (0.66) PTGS1TNFSF11CYP4F2CYP4A11ALDH1A1
SCHEMBL1706883 0.78 PTGS2 (0.64) TUBB4ATUBBTUBA3CTUBA1BTUBA4A
SCHEMBL2635399 0.78 KMT2A (0.50) TUBB4ATUBBTUBA3CTUBA1BTUBA4A
SCHEMBL13775501 0.77 ACHE (0.58) TUBB4ATUBBTUBA3CTUBA1BTUBA4A
SCHEMBL3326825 0.77 TUBB4A (0.63) TUBB4ATUBBTUBA3CTUBA1BTUBA4A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-106431855-A Halogen or nitrogen-containing group substituted bibenzyl analog, preparation method and uses thereof 中国药科大学 2017-02-22 CN disclosed
US-6376510-B1 ADMINISTERING A ALKOXY- AND ACYLOXY-SUBSTITUTED ARALKYL AND ARALKENYL BIS QUATERNARY AMMONIUM DERIVATIVES OF CYCLIC ALKANOL DIESTERS TO A HUMAN AS MUSCLE RELAXANTS NEWLAXANT LLC 2002-04-23 US disclosed
US-6274623-B1 DI- OR POLY-ALKOXY-OR ACYLOXY-SUBSTITUTED ARALKYL AND ARAKENYL QUATERNARY AMMONIUM DERIVATIVES OF CYCLIC AMINOALKANOL DIESTERS SUCH AS BIS(N-(3,4-DIPROPIONYLOXY-BENZYL)GRANATANINIUM-3-ALPHA-YL)ADIPATE DIBROMIDE NEWLAXANT LLC 2001-08-14 US disclosed
US-6274757-B1 REACTING AN HYDROXY AMINE CORRESPONDING COMPOUND WITH DICHLORO COMPOUND NEWLAXANT LLC 2001-08-14 US disclosed
US-5990124-A ALKOXY AND/OR ACYLOXY DI- AND POLY-SUBSTITUTED ARALKYL AND ARALKENYL BIS-QUATERNARY AMMONIUM DERIVATIVES OF CYCLIC ALKANOL DIESTERS; SUCH AS BIS(N-(4-ACETOXY-3-METHOXYBENZYL) TROPANIUM-3-YL)-3,6-ENDOMETHYLENE-1,2,3,6-TETRAHYDROPHTHALATE GYERMEK LASZLO (US) 1999-11-23 US disclosed