SCHEMBL162513

SCHEMBL162513

C#CC(O)(c1ccccc1)c1ccc(N2CCOCC2)cc1

nearest known ligand 0.51

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 2/20 0.51
PKM P14618 1/20 0.45
TSHR P16473 1/20 0.45
ALDH1A1 P00352 7/20 0.44
MAPT P10636 6/20 0.44
SMN1; SMN2 Q16637 6/20 0.44
NPC1 O15118 4/20 0.44
RAB9A P51151 4/20 0.44
MEN1 O00255 3/20 0.44
KMT2A Q03164 3/20 0.44
HTT P42858 2/20 0.44
CYP1A2 P05177 1/20 0.44
KCNA5 P22460 2/20 0.43
KDM4E B2RXH2 2/20 0.42
ALOX15 P16050 2/20 0.42
HSD17B10 Q99714 2/20 0.42
USP2 O75604 1/20 0.42
TP53 P04637 1/20 0.42
MAPK1 P28482 1/20 0.42
AKR1C3 P42330 3/20 0.42

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
SCHEMBL28370082 1.00 LMNA (0.51) LMNAPKMTSHRALDH1A1MAPT
SCHEMBL24620659 0.94 MAPT (0.47) LMNATSHRALDH1A1MAPTSMN1; SMN2
SCHEMBL25954142 0.94 MAPT (0.47) LMNATSHRALDH1A1MAPTSMN1; SMN2
SCHEMBL20643563 0.88 MAPT (0.44) LMNAALDH1A1MAPTNPC1RAB9A
SCHEMBL1793404 0.88 MAPT (0.46) LMNAPKMTSHRALDH1A1MAPT
SCHEMBL10018215 0.87 TP53 (0.50) LMNAPKMALDH1A1MAPTNPC1
SCHEMBL1962637 0.87 AKR1C3 (0.49) LMNAALDH1A1MAPTSMN1; SMN2MEN1
SCHEMBL3143230 0.86 RAB9A (0.46) LMNAPKMTSHRALDH1A1MAPT
SCHEMBL21940997 0.86 RAB9A (0.46) LMNAPKMTSHRALDH1A1MAPT
SCHEMBL25954146 0.85 SLC13A5 (0.43) LMNAALDH1A1MAPTSMN1; SMN2NPC1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4313996-B1 INDENONAPHTHOPYRANS HAVING TRIALKYLSILYL AND ETHYLENICALLY UNSATURATED GROUPS TRANSITIONS OPTICAL LTD (IE) 2026-05-06 EP disclosed
US-20240376132-A1 Indenonaphthopyrans Having Trialkylsilyl and Ethylenically Unsaturated Groups TRANSITIONS OPTICAL, LTD. (IE) 2024-11-14 US disclosed
EP-3621958-B9 PHOTOCHROMIC INDENO FUSED PHENANTHRENOPYRAN COMPOUNDS TRANSITIONS OPTICAL LTD (IE) 2024-09-25 EP disclosed
EP-3621958-B1 PHOTOCHROMIC INDENO FUSED PHENANTHRENOPYRAN COMPOUNDS TRANSITIONS OPTICAL LTD (IE) 2024-07-10 EP disclosed
EP-4313996-A1 INDENONAPHTHOPYRANS HAVING TRIALKYLSILYL AND ETHYLENICALLY UNSATURATED GROUPS Transitions Optical, Ltd. (IE) 2024-02-07 EP disclosed
US-11874434-B2 Ophthalmic devices comprising photochromic materials with reactive substituents JOHNSON & JOHNSON VISION CARE, INC. (US) 2024-01-16 US disclosed
CN-117043168-A Indenonaphthopyrans having trialkylsilyl groups and ethylenically unsaturated groups 光学转变有限公司 2023-11-10 CN disclosed
EP-3898636-B9 INDOLONAPHTHOPYRANS TRANSITIONS OPTICAL LTD (IE) 2023-11-08 EP disclosed
CN-110730778-B Photochromic indeno-fused phenanthropyran compounds 光学转变有限公司 2023-09-12 CN disclosed
EP-3898636-B1 INDOLONAPHTHOPYRANS TRANSITIONS OPTICAL LTD (IE) 2023-08-30 EP disclosed
WO-2001019813-A1 NOVEL INDENO-FUSED PHOTOCHROMIC NAPHTHOPYRANS TRANSITIONS OPTICAL, INC. (US) 2001-03-22 WO disclosed
EP-1036077-A1 PHOTOCHROMIC PYRANO-FUSED NAPHTHOPYRANS TRANSITIONS OPTICAL, INC. (US) 2000-09-20 EP disclosed
US-6106744-A HAVING A SUBSTITUTED OR UNSUBSTITUTED ?S? PYRAN RING, THE 3,4 POSITIONS OF WHICH ARE FUSED TO THE F SIDE OF THE NAPHTHO PORTION OF THE NAPHTHOPYRAN, AND CERTAIN SUBSTITUENTS AT THE 2-POSITION OF THE ?T? PYRAN RING. PPG INDUSTRIES OHIO, INC. (US) 2000-08-22 US disclosed
EP-1000025-A1 SUBSTITUTED NAPHTHOPYRANS TRANSITIONS OPTICAL, INC. (US) 2000-05-17 EP disclosed
US-6022495-A FOR OPTICAL APPLICATIONS TRANSITIONS OPTICAL, INC. (US) 2000-02-08 US disclosed
WO-2000002884-A2 PHOTOCHROMIC BENZOPYRANO-FUSED NAPHTHOPYRANS TRANSITIONS OPTICAL, INC. (US) 2000-01-20 WO disclosed
WO-1999031081-A1 PH SENSITIVE PHOTOCHROMIC DYES JAMES ROBINSON LIMITED (GB) 1999-06-24 WO disclosed
WO-1999028323-A1 NOVEL PHOTOCHROMIC PYRANO-FUSED NAPHTHOPYRANS TRANSITIONS OPTICAL, INC. (US) 1999-06-10 WO disclosed
WO-1998055457-A1 SUBSTITUTED NAPHTHOPYRANS TRANSITIONS OPTICAL, INC. (US) 1998-12-10 WO disclosed
US-5658500-A REVERSIBLE PHOTOCHROMIC COMPOUNDS TRANSITIONS OPTICAL, INC. (US) 1997-08-19 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 (1 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-20240376132-A1 Indenonaphthopyrans Having Trialkylsilyl and Ethylenically Unsaturated Groups B3GNT2, ERLIN1, RPN1 LMNA 1851/4885PKM 3022/4885TSHR 3338/4885

“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.