SCHEMBL5752998

SCHEMBL5752998

COc1ccc2cc(Br)ccc2c1C

nearest known ligand 0.55

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
POLB P06746 1/20 0.55
LMNA P02545 5/20 0.55
SMN1; SMN2 Q16637 4/20 0.55
L3MBTL1 Q9Y468 3/20 0.55
RXFP1 Q9HBX9 5/20 0.52
KMT2A Q03164 2/20 0.48
KDM4E B2RXH2 2/20 0.48
MEN1 O00255 1/20 0.48
MAPT P10636 1/20 0.47
NCEH1 Q6PIU2 2/20 0.45
ALDH1A1 P00352 2/20 0.43
IDO1 P14902 1/20 0.43
TDO2 P48775 1/20 0.43
CYP19A1 P11511 1/20 0.39
CYP11B1 P15538 1/20 0.39
CYP11B2 P19099 1/20 0.39
HPGD P15428 1/20 0.39
TSHR P16473 1/20 0.39
HSD17B10 Q99714 1/20 0.39
KDM2B Q8NHM5 1/20 0.39

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
SCHEMBL7817956 0.88 POLB (0.59) POLBLMNASMN1; SMN2L3MBTL1RXFP1
SCHEMBL3019686 0.83 NCEH1 (0.58) POLBLMNASMN1; SMN2L3MBTL1RXFP1
SCHEMBL30638066 0.83 MAPT (0.55) POLBLMNASMN1; SMN2L3MBTL1RXFP1
SCHEMBL3829305 0.83 MAPT (0.55) POLBLMNASMN1; SMN2L3MBTL1RXFP1
SCHEMBL5749500 0.81 IDO1 (0.57) POLBLMNASMN1; SMN2L3MBTL1RXFP1
SCHEMBL806517 0.81 ACHE (0.54) POLBLMNAL3MBTL1KMT2AKDM4E
SCHEMBL29262551 0.81 RXFP1 (0.63) POLBLMNASMN1; SMN2L3MBTL1RXFP1
SCHEMBL3160115 0.80 POLB (0.50) POLBLMNASMN1; SMN2L3MBTL1RXFP1
SCHEMBL8395861 0.80 POLB (0.50) POLBLMNASMN1; SMN2L3MBTL1RXFP1
SCHEMBL13781592 0.80 NCEH1 (0.60) POLBLMNASMN1; SMN2L3MBTL1RXFP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114015459-A Double-naphthalene monomer-containing liquid crystal and preparation method and application thereof 中节能万润股份有限公司 2022-02-08 CN claimed
CN-114015459-B Liquid crystal containing dinaphthyl monomer, and preparation method and application thereof 中节能万润股份有限公司 2023-09-29 CN disclosed
CN-114015459-A Double-naphthalene monomer-containing liquid crystal and preparation method and application thereof 中节能万润股份有限公司 2022-02-08 CN disclosed
EP-3242872-B1 (PIPERIDIN-3-YL)(NAPHTHALEN-2-YL)METHANONE DERIVATIVES AND RELATED COMPOUNDS AS INHIBITORS OF THE HISTONE DEMETHYLASE KDM2B FOR THE TREATMENT OF CANCER GENENTECH INC (US) 2019-07-03 EP disclosed
US-20180022727-A1 THERAPEUTIC COMPOUNDS AND USES THEREOF GENENTECH, INC. (US) 2018-01-25 US disclosed
EP-3242872-A1 (PIPERIDIN-3-YL)(NAPHTHALEN-2-YL)METHANONE DERIVATIVES AND RELATED COMPOUNDS AS INHIBITORS OF THE HISTONE DEMETHYLASE KDM2B FOR THE TREATMENT OF CANCER Genentech, Inc. (US) 2017-11-15 EP disclosed
WO-2016112284-A1 (PIPERIDIN-3-YL)(NAPHTHALEN-2-YL)METHANONE DERIVATIVES AND RELATED COMPOUNDS AS INHIBITORS OF THE HISTONE DEMETHYLASE KDM2B FOR THE TREATMENT OF CANCER GENENTECH, INC. (US) 2016-07-14 WO disclosed
WO-2016112284-A1 (PIPERIDIN-3-YL)(NAPHTHALEN-2-YL)METHANONE DERIVATIVES AND RELATED COMPOUNDS AS INHIBITORS OF THE HISTONE DEMETHYLASE KDM2B FOR THE TREATMENT OF CANCER GENENTECH, INC. (US) 2016-07-14 WO disclosed
US-7959990-B2 Adjustment of liquid crystals; oligomers, dendrimers, or polymer in solution is applied to support; crosslinking by radiation or polarized light ROLIC AG (CH) 2011-06-14 US disclosed
US-20080274304-A1 Functionalized Photoreactive Compounds ROLIC AG (CH) 2008-11-06 US disclosed
US-20030236274-A1 Naphthalene derivatives, their production and use TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2003-12-25 US disclosed
US-6573289-B1 Naphthalene derivatives, their production and use TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 2003-06-03 US disclosed
EP-1073640-A1 NAPHTHALENE DERIVATIVES, THEIR PRODUCTION AND USE Takeda Chemical Industries, Ltd. (JP) 2001-02-07 EP disclosed
EP-0710367-B1 PHOTOCHROMIC SUBSTITUTED NAPHTHOPYRAN COMPOUNDS PPG IND OHIO INC (US) 2000-08-30 EP disclosed
WO-1999054309-A1 NAPHTHALENE DERIVATIVES, THEIR PRODUCTION AND USE TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1999-10-28 WO disclosed
US-5637262-A REVERSIBLE PHOTOCHROMIC DYES FOR OPHTHALMIC LENSES TRANSITIONS OPTICAL, INC. (US) 1997-06-10 US disclosed
EP-0710367-A4 1996-05-15 EP disclosed
EP-0710367-A1 PHOTOCHROMIC SUBSTITUTED NAPHTHOPYRAN COMPOUNDS PPG INDUSTRIES, INC. (US) 1996-05-08 EP disclosed
US-5466398-A Photochromic substituted naphthopyran compounds TRANSITIONS OPTICAL, INC. (US) 1995-11-14 US disclosed
WO-1995000867-A1 PHOTOCHROMIC SUBSTITUTED NAPHTHOPYRAN COMPOUNDS PPG INDUSTRIES, INC. (US) 1995-01-05 WO 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 (3 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-20030236274-A1 Naphthalene derivatives, their production and use CYP17A1, CYP21A2, HSD17B1 POLB 2225/4885LMNA 3058/4885SMN1; SMN2 3733/4885
US-20080274304-A1 Functionalized Photoreactive Compounds PCNA, PIN1, MAP1LC3C POLB 610/4885LMNA 1132/4885SMN1; SMN2 4506/4885
US-20180022727-A1 THERAPEUTIC COMPOUNDS AND USES THEREOF KDM1B, KDM6B, KDM2B POLB 810/4885LMNA 1915/4885SMN1; SMN2 660/4885

“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.