SCHEMBL8675813

SCHEMBL8675813

C[SiH](C)Oc1c(C(C)(C)C)ccc2c1C(=O)c1ccccc1-2

nearest known ligand 0.41

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NPC1 O15118 6/20 0.41
RAB9A P51151 6/20 0.41
SMN1; SMN2 Q16637 6/20 0.41
ALDH1A1 P00352 7/20 0.38
PLA2G1B P04054 2/20 0.38
ATG4B Q9Y4P1 2/20 0.38
CASP3 P42574 2/20 0.38
SENP7 Q9BQF6 2/20 0.38
SENP6 Q9GZR1 2/20 0.38
L3MBTL1 Q9Y468 2/20 0.38
NFKB1 P19838 1/20 0.38
NFKB2 Q00653 1/20 0.38
RELA Q04206 1/20 0.38
SENP8 Q96LD8 1/20 0.38
MAPT P10636 9/20 0.38
MEN1 O00255 4/20 0.37
KMT2A Q03164 4/20 0.37
KDM4E B2RXH2 3/20 0.37
TDP1 Q9NUW8 2/20 0.37
USP2 O75604 1/20 0.37

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
SCHEMBL18789612 0.73 ALDH1A1 (0.48) NPC1RAB9ASMN1; SMN2ALDH1A1PLA2G1B
SCHEMBL12445275 0.72 MAPT (0.50) NPC1RAB9ASMN1; SMN2ALDH1A1PLA2G1B
SCHEMBL7622508 0.69 PDE4B (0.40) ALDH1A1L3MBTL1MAPTKDM4ETDP1
SCHEMBL3420316 0.68 ALDH1A1 (0.49) NPC1RAB9ASMN1; SMN2ALDH1A1PLA2G1B
SCHEMBL22351864 0.68 ALDH1A1 (0.50) NPC1RAB9ASMN1; SMN2ALDH1A1PLA2G1B
SCHEMBL31322264 0.67 ALDH1A1 (0.47) NPC1RAB9ASMN1; SMN2ALDH1A1PLA2G1B
SCHEMBL7249419 0.67 ALDH1A1 (0.41) ALDH1A1L3MBTL1TDP1S1PR1TSHR
SCHEMBL9696405 0.66 CA2 (0.38) ALDH1A1TDP1TSHR
Anthraquinone SCHEMBL29222026 0.65 ADORA2A (0.52) NPC1RAB9ASMN1; SMN2ALDH1A1PLA2G1B
SCHEMBL50547 0.65 ADORA2A (0.52) NPC1RAB9ASMN1; SMN2ALDH1A1PLA2G1B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5707559-A PROVIDING A STABLE 1,2-DIOXETANE WHICH FORMS INTERMEDIATE UNSTABLE COMPOUNDS WHEN TRIGGERED TO REMOVE BLOCKING GROUPS BY ACTIVATING AGENT SO THAT UNSTABLE COMPOUND DECOMPOSES TO FORM LIGHT AND TWO CARBONYL COMPOUNDS TROPIX, INC. (US) 1998-01-13 US disclosed
EP-0595369-B1 Alkene compounds TROPIX INC (US) 1996-12-04 EP disclosed
US-5386017-A Can be converted to stable aryl substituted 1,2-dioxetanes which decompose when activated to produce light and carbonyl compounds BOARD OF GOVERNORS OF WAYNE STATE UNIVERSITY (US) 1995-01-31 US disclosed
EP-0254051-B1 Chemiluminescent 1,2-dioxetane compounds UNIV WAYNE STATE (US) 1994-08-31 EP disclosed
EP-0595369-A1 Alkene compounds TROPIX, INC. (US) 1994-05-04 EP disclosed
US-4962192-A Chemiluminescent 1,2-dioxetane compounds BOARD OF GOVERNORS OF WAYNE STATE UNIVERSITY (US) 1990-10-09 US disclosed
US-4857652-A Chemiluminescent 1,2-dioxetane compounds BOARD OF GOVERNORS OF WAYNE STATE UNIVERSITY (US) 1989-08-15 US disclosed
EP-0254051-A2 Chemiluminescent 1,2-dioxetane compounds THE BOARD OF GOVERNORS OF WAYNE STATE UNIVERSITY (US) 1988-01-27 EP disclosed