SCHEMBL5178952

SCHEMBL5178952

COc1ccc2c(C)c(CO)c3c(c2c1)OC(c1ccccc1)(c1ccccc1)C=C3

nearest known ligand 0.36

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 6/20 0.36
KMT2A Q03164 6/20 0.36
LMNA P02545 2/20 0.36
CYP2C9 P11712 2/20 0.36
TSHR P16473 2/20 0.36
KDM4E B2RXH2 2/20 0.36
ALDH1A1 P00352 2/20 0.36
HPGD P15428 1/20 0.36
CYP2C19 P33261 1/20 0.36
HTT P42858 1/20 0.36
HSD17B10 Q99714 1/20 0.36
PIN1 Q13526 1/20 0.34
NPC1 O15118 4/20 0.33
RAB9A P51151 4/20 0.33
CYP1A2 P05177 1/20 0.33
CYP2D6 P10635 1/20 0.33
NFKB1 P19838 1/20 0.33
HIF1A Q16665 1/20 0.33
NPSR1 Q6W5P4 1/20 0.33
MAPT P10636 1/20 0.32

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
SCHEMBL6651812 0.94 KDM4E (0.37) MEN1KMT2ALMNACYP2C9TSHR
SCHEMBL29565106 0.94 KDM4E (0.37) MEN1KMT2ALMNACYP2C9TSHR
SCHEMBL1984131 0.88 EDNRA (0.33) MEN1KMT2ALMNACYP2C9TSHR
SCHEMBL6172997 0.82 PLA2G2A (0.38) MEN1KMT2ALMNACYP2C9TSHR
SCHEMBL12377285 0.78 BRAF (0.37) MEN1KMT2ALMNACYP2C9KDM4E
SCHEMBL6650937 0.77 GPR84 (0.37) LMNACYP2C9KDM4EALDH1A1HPGD
SCHEMBL29566136 0.77 GPR84 (0.37) LMNACYP2C9KDM4EALDH1A1HPGD
SCHEMBL5107553 0.77 AKR1C3 (0.37) MEN1KMT2ALMNACYP2C9TSHR
SCHEMBL30914186 0.77 MAPT (0.36) MEN1KMT2ALMNATSHRKDM4E
SCHEMBL13726047 0.77 BRAF (0.37) MEN1KMT2ALMNACYP2C9KDM4E

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
EP-1776436-B1 PHOTOCHROMIC MATERIALS TRANSITIONS OPTICAL INC (US) 2019-05-08 EP claimed
EP-0894275-B1 PHOTOCHROMIC NAPHTHOPYRAN COMPOSITIONS OF IMPROVED FATIGUE RESISTANCE TRANSITIONS OPTICAL INC (US) 2007-10-03 EP claimed
EP-0890119-B1 PHOTOCHROMIC NAPHTHOPYRAN COMPOSITIONS OF NEUTRAL COLOR TRANSITIONS OPTICAL INC (US) 2007-06-20 EP claimed
EP-1776436-A1 PHOTOCHROMIC MATERIALS TRANSITIONS OPTICAL, INC. (US) 2007-04-25 EP claimed
WO-2006022825-A1 PHOTOCHROMIC MATERIALS TRANSITIONS OPTICAL, INC. (US) 2006-03-02 WO claimed
US-20060022176-A1 Reaction product of a ring-opening cyclic ester or carbonate and a photochromic initiator, especially a naphtho[1,2-b]quinone with one or more hydroxy groups, e.g., (1) 3,3-di(4-methoxyphenyl)-6,7-dimethoxy-13-methyl-13-(2-(2-hydroxyethoxy)ethoxy)-3H,13H-indeno[2,1-f]naphtho[1,2-b]pyran. TRANSITIONS OPTICAL LIMITED (IE) 2006-02-02 US claimed
EP-0894275-A4 PHOTOCHROMIC NAPHTHOPYRAN COMPOSITIONS OF IMPROVED FATIGUE RESISTANCE TRANSITIONS OPTICAL INC (US) 2000-03-29 EP claimed
CN-1216113-A Phtochromic naphthopyran compositions of neutral color OPTICAL CONVERSION INC (US) 1999-05-05 CN claimed
EP-0894275-A1 PHOTOCHROMIC NAPHTHOPYRAN COMPOSITIONS OF IMPROVED FATIGUE RESISTANCE TRANSITIONS OPTICAL, INC. (US) 1999-02-03 EP claimed
US-5770115-A POLYPHENOLIC ANTIOXIDANT, UV ABSORBER, HINDERED AMINE LIGHT STABILIZER, NAPHTHOPYRAN DYE PPG INDUSTRIES, INC. (US) 1998-06-23 US claimed
US-5753146-A CONTAINING ATLEAST TWO PHOTOCHROMATIC COMPOUNDS, SUCH AS 3(H)-NAPHTHO(2,1-B)PYRANS AND 2(H)-NAPHTHO(1,2-B)PYRANS, FREE OF AMINO SUBSTITUTED ARYL GROUPS ON CARBON ATOM ADJACENT TO THE OXYGEN ATOM OF PYRAN RING, EXPOSED TO ULTRAVIOLET RAYS TRANSITIONS OPTICAL, INC. (US) 1998-05-19 US claimed
WO-1997040409-A1 PHOTOCHROMIC NAPHTHOPYRAN COMPOSITIONS OF IMPROVED FATIGUE RESISTANCE TRANSITIONS OPTICAL, INC. (US) 1997-10-30 WO claimed
US-11414534-B2 Multifunctional optically highly transparent films and method for their production ISLAND POLYMER INDUSTRIES GMBH (DE) 2022-08-16 US disclosed
CN-107636056-B Multifunctional optical high-transparency film and production method thereof 艾兰德高分子工业有限公司 2021-11-19 CN disclosed
US-20180265680-A1 MULTIFUNCTIONAL OPTICALLY HIGHLY TRANSPARENT FILMS AND METHOD FOR THEIR PRODUCTION ISLAND POLYMER INDUSTRIES GMBH (DE) 2018-09-20 US disclosed
EP-3262107-A1 MULTIFUNCTIONAL OPTICALLY HIGHLY TRANSPARENT FILMS, AND A METHOD FOR PRODUCING SAME Island Polymer Industries GmbH (DE) 2018-01-03 EP disclosed
EP-0890119-B1 PHOTOCHROMIC NAPHTHOPYRAN COMPOSITIONS OF NEUTRAL COLOR TRANSITIONS OPTICAL INC (US) 2007-06-20 EP disclosed
CN-1216113-A Phtochromic naphthopyran compositions of neutral color OPTICAL CONVERSION INC (US) 1999-05-05 CN disclosed
US-5770115-A POLYPHENOLIC ANTIOXIDANT, UV ABSORBER, HINDERED AMINE LIGHT STABILIZER, NAPHTHOPYRAN DYE PPG INDUSTRIES, INC. (US) 1998-06-23 US disclosed
US-5753146-A CONTAINING ATLEAST TWO PHOTOCHROMATIC COMPOUNDS, SUCH AS 3(H)-NAPHTHO(2,1-B)PYRANS AND 2(H)-NAPHTHO(1,2-B)PYRANS, FREE OF AMINO SUBSTITUTED ARYL GROUPS ON CARBON ATOM ADJACENT TO THE OXYGEN ATOM OF PYRAN RING, EXPOSED TO ULTRAVIOLET RAYS TRANSITIONS OPTICAL, INC. (US) 1998-05-19 US disclosed