SCHEMBL3760690

SCHEMBL3760690

CCCc1ccc(OC(=O)c2ccccc2)cc1

nearest known ligand 0.61

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 6/20 0.60
PLA2G1B P04054 1/20 0.60
ATG4B Q9Y4P1 1/20 0.60
MAPT P10636 7/20 0.57
THRB P10828 3/20 0.57
TDP1 Q9NUW8 2/20 0.57
ALDH1A1 P00352 2/20 0.57
L3MBTL1 Q9Y468 1/20 0.57
PKM P14618 1/20 0.57
PARP10 Q53GL7 1/20 0.56
RAB9A P51151 3/20 0.52
SMN1; SMN2 Q16637 2/20 0.52
NPC1 O15118 1/20 0.52
CASP3 P42574 1/20 0.52
SENP8 Q96LD8 1/20 0.52
SENP7 Q9BQF6 1/20 0.52
SENP6 Q9GZR1 1/20 0.52
MEN1 O00255 3/20 0.51
LMNA P02545 1/20 0.50
MAOB P27338 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
SCHEMBL3771392 0.93 KMT2A (0.56) KMT2APLA2G1BATG4BMAPTTHRB
SCHEMBL10633416 0.91 THRB (0.62) KMT2APLA2G1BATG4BMAPTTHRB
SCHEMBL30354554 0.91 THRB (0.62) KMT2APLA2G1BATG4BMAPTTHRB
SCHEMBL8384448 0.90 ALDH1A1 (0.54) KMT2APLA2G1BATG4BMAPTTHRB
SCHEMBL11395782 0.89 THRB (0.60) KMT2AMAPTTHRBTDP1ALDH1A1
SCHEMBL6013651 0.89 KMT2A (0.58) KMT2APLA2G1BATG4BMAPTTHRB
SCHEMBL11124363 0.89 MAPT (0.55) KMT2APLA2G1BATG4BMAPTTHRB
SCHEMBL4905240 0.88 KMT2A (0.62) KMT2AMAPTTDP1ALDH1A1L3MBTL1
SCHEMBL11579348 0.88 THRB (0.59) KMT2AMAPTTHRBTDP1ALDH1A1
SCHEMBL28798935 0.88 THRB (0.59) KMT2AMAPTTHRBTDP1ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7847998-B2 Polarizing, photochromic devices and methods of making the same TRANSITIONS OPTICAL, INC. (US) 2010-12-07 US claimed
EP-2969499-A1 METHOD OF PREPARING PHOTOCHROMIC-DICHROIC FILMS HAVING REDUCED OPTICAL DISTORTION Transitions Optical, Inc. (US) 2016-01-20 EP disclosed
CN-102668157-B Organic electroluminescence element, manufacturing method thereof, and organic electroluminescence display device SHARP KK 2014-11-26 CN disclosed
WO-2014158802-A1 METHOD OF PREPARING PHOTOCHROMIC-DICHROIC FILMS HAVING REDUCED OPTICAL DISTORTION TRANSITIONS OPTICAL, INC. (US) 2014-10-02 WO disclosed
US-20140265010-A1 METHOD OF PREPARING PHOTOCHROMIC-DICHROIC FILMS HAVING REDUCED OPTICAL DISTORTION TRANSITIONS OPTICAL LIMITED (IE) 2014-09-18 US disclosed
US-20140264979-A1 METHOD OF PREPARING PHOTOCHROMIC-DICHROIC FILMS HAVING REDUCED OPTICAL DISTORTION TRANSITIONS OPTICAL LIMITED (IE) 2014-09-18 US disclosed
US-20140078583-A1 Photochromic Article Having At Least Partially Crossed Polarized Photochromic-Dichroic And Fixed-Polarized Layers TRANSITIONS OPTICAL, INC. (US) 2014-03-20 US disclosed
US-8582192-B2 Polarizing photochromic articles TRANSITIONS OPTICAL, INC. (US) 2013-11-12 US disclosed
CN-102668157-A Organic electroluminescence element, manufacturing method thereof, and organic electroluminescence display device SHARP KK 2012-09-12 CN disclosed
US-7582749-B2 Photochromic compounds TRANSITIONS OPTICAL, INC. (US) 2009-09-01 US disclosed
US-20080123172-A1 POLARIZING, PHOTOCHROMIC DEVICES AND METHODS OF MAKING THE SAME TRANSITIONS OPTICAL LIMITED (IE) 2008-05-29 US disclosed
US-20080096049-A1 capable of switching between the two states in response to at least actinic radiation; thermally reversible TRANSITIONS OPTICAL, INC. (US) 2008-04-24 US disclosed
US-20080096048-A1 Thermally reversible; absorption ratio greater than 2.3 TRANSITIONS OPTICAL, INC. (US) 2008-04-24 US disclosed
US-7349137-B2 Polarizing, photochromic devices and methods of making the same PPG INDUSTRIES OHIO, INC. (US) 2008-03-25 US disclosed
US-20080051575-A1 capable of switching between the two states in response to at least actinic radiation; thermally reversible TRANSITIONS OPTICAL ,INC. (US) 2008-02-28 US disclosed
US-20080045704-A1 Thermally reversible; absorption ratio greater than 2.3; cell method TRANSITIONS OPTICAL, INC. (US) 2008-02-21 US disclosed
US-7256921-B2 Polarizing, photochromic devices and methods of making the same TRANSITIONS OPTICAL, INC. (US) 2007-08-14 US disclosed
US-20070053048-A1 Polirizing, photochromic devices and methods of making the same TRANSITIONS OPTICAL LIMITED (IE) 2007-03-08 US disclosed
US-20050012998-A1 Polarizing, photochromic devices and methods of making the same TRANSITIONS OPTICAL LIMITED (IE) 2005-01-20 US disclosed
CN-1262276-A Phosphine sulfide preparing process and use thereof MITSUI CHEMICALS INC (JP) 2000-08-09 CN disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (4 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20080045704-A1 Thermally reversible; absorption ratio greater than 2.3; cell method CCND3, CCND1, CCND2 KMT2A 1511/4885PLA2G1B 3900/4885ATG4B 4729/4885
US-20080096048-A1 Thermally reversible; absorption ratio greater than 2.3 CCND1, CCND3, CCND2 KMT2A 1838/4885PLA2G1B 3754/4885ATG4B 4705/4885
US-20080051575-A1 capable of switching between the two states in response to at least actinic radiation; thermally reversible CCND1, CCND2, CCNE1 KMT2A 1830/4885PLA2G1B 2027/4885ATG4B 4772/4885
US-20080096049-A1 capable of switching between the two states in response to at least actinic radiation; thermally reversible CCND1, CCND2, CCNE1 KMT2A 1830/4885PLA2G1B 2027/4885ATG4B 4772/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.