SCHEMBL3760693

SCHEMBL3760693

CCCc1ccccc1OC(=O)c1ccccc1

nearest known ligand 0.58

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NPSR1 Q6W5P4 2/20 0.58
KMT2A Q03164 4/20 0.54
MAPT P10636 2/20 0.54
SMN1; SMN2 Q16637 2/20 0.54
SLC6A3 Q01959 1/20 0.53
LMNA P02545 2/20 0.50
THRA P10827 1/20 0.48
THRB P10828 1/20 0.48
ESR1 P03372 2/20 0.47
ESR2 Q92731 2/20 0.47
MEN1 O00255 2/20 0.47
JAK2 O60674 1/20 0.47
USP2 O75604 1/20 0.47
GAA P10253 1/20 0.47
ALOX15 P16050 1/20 0.47
HSD17B10 Q99714 1/20 0.47
METAP2 P50579 1/20 0.44
METAP1 P53582 1/20 0.44
HDAC6 Q9UBN7 1/20 0.44
TOP1 P11387 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
SCHEMBL4631646 0.94 NPSR1 (0.53) NPSR1KMT2AMAPTSMN1; SMN2SLC6A3
SCHEMBL10923583 0.90 NPSR1 (0.49) NPSR1KMT2AMAPTSMN1; SMN2SLC6A3
SCHEMBL8778657 0.90 THRA (0.56) NPSR1KMT2AMAPTSMN1; SMN2SLC6A3
SCHEMBL434556 0.88 KMT2A (0.59) NPSR1KMT2AMAPTSMN1; SMN2SLC6A3
SCHEMBL29412194 0.88 KMT2A (0.59) NPSR1KMT2AMAPTSMN1; SMN2SLC6A3
SCHEMBL8405141 0.88 NPSR1 (0.53) NPSR1KMT2AMAPTSMN1; SMN2SLC6A3
SCHEMBL2484906 0.88 KMT2A (0.49) NPSR1KMT2AMAPTSMN1; SMN2SLC6A3
SCHEMBL28345751 0.88 THRA (0.64) NPSR1KMT2AMAPTSMN1; SMN2SLC6A3
SCHEMBL11579345 0.88 THRA (0.64) NPSR1KMT2AMAPTSMN1; SMN2SLC6A3
SCHEMBL8390875 0.88 THRA (0.64) NPSR1KMT2AMAPTSMN1; SMN2SLC6A3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-107014914-A A kind of method of formula isomers and nitrobenzoyl phenyl propane compounds while Analyze & separate FCE-20124 is revived 重庆医药高等专科学校 2017-08-04 CN claimed
US-7847998-B2 Polarizing, photochromic devices and methods of making the same TRANSITIONS OPTICAL, INC. (US) 2010-12-07 US claimed
CN-107014914-A A kind of method of formula isomers and nitrobenzoyl phenyl propane compounds while Analyze & separate FCE-20124 is revived 重庆医药高等专科学校 2017-08-04 CN disclosed
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-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

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 NPSR1 3046/4885KMT2A 1511/4885MAPT 4145/4885
US-20080096048-A1 Thermally reversible; absorption ratio greater than 2.3 CCND1, CCND3, CCND2 NPSR1 2873/4885KMT2A 1838/4885MAPT 4150/4885
US-20080051575-A1 capable of switching between the two states in response to at least actinic radiation; thermally reversible CCND1, CCND2, CCNE1 NPSR1 3617/4885KMT2A 1830/4885MAPT 4085/4885
US-20080096049-A1 capable of switching between the two states in response to at least actinic radiation; thermally reversible CCND1, CCND2, CCNE1 NPSR1 3617/4885KMT2A 1830/4885MAPT 4085/4885

“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.