SCHEMBL9898532

SCHEMBL9898532

CCCCOc1cccc(C(=O)c2ccccc2)c1OCCCC

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 3/20 0.52
MAPT P10636 3/20 0.52
L3MBTL1 Q9Y468 3/20 0.52
CNR1 P21554 3/20 0.50
CNR2 P34972 3/20 0.50
MEN1 O00255 1/20 0.50
NR1I2 O75469 1/20 0.50
CHRM2 P08172 1/20 0.50
CYP3A4 P08684 1/20 0.50
ADRA2A P08913 1/20 0.50
OPRK1 P41145 1/20 0.50
HTR2B P41595 1/20 0.50
SLC6A3 Q01959 1/20 0.50
KMT2A Q03164 1/20 0.50
HDAC6 Q9UBN7 1/20 0.50
CCNB2 O95067 2/20 0.49
CCNE2 O96020 2/20 0.49
CDK1 P06493 2/20 0.49
CCNB1 P14635 2/20 0.49
CCNE1 P24864 2/20 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
SCHEMBL28330270 0.97 LMNA (0.55) LMNAMAPTL3MBTL1CNR1CNR2
SCHEMBL4479542 0.94 LMNA (0.58) LMNAMAPTL3MBTL1CNR1CNR2
SCHEMBL28209598 0.93 CCNB2 (0.52) LMNAMAPTL3MBTL1CNR1CNR2
SCHEMBL9075084 0.89 LTB4R (0.54) LMNAMAPTMEN1NR1I2CHRM2
SCHEMBL5163358 0.89 CNR1 (0.50) LMNAMAPTL3MBTL1CNR1CNR2
SCHEMBL5163351 0.88 LMNA (0.56) LMNAMAPTL3MBTL1CNR1CNR2
SCHEMBL29518968 0.88 DRD2 (0.59) LMNAMAPTL3MBTL1CNR1CNR2
SCHEMBL18917587 0.88 DRD2 (0.59) LMNAMAPTL3MBTL1CNR1CNR2
Bicarbonate SCHEMBL28775865 0.87 DRD2 (0.58) LMNAMAPTL3MBTL1CNR1CNR2
SCHEMBL4625163 0.86 CNR1 (0.44) LMNAMAPTL3MBTL1CNR1CNR2

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 5 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-106471043-A The polysiloxanes of chromophore functionalization of UV activity and the copolymer being made from 莫门蒂夫性能材料股份有限公司 2017-03-01 CN claimed
CN-110521290-B Photosensitive resin composition, dry film using same, printed wiring board, and method for producing printed wiring board 日立化成株式会社 2022-04-05 CN disclosed
US-9028728-B2 Photochromic materials that include indeno-fused naphthopyrans TRANSITIONS OPTICAL, INC. (US) 2015-05-12 US disclosed
WO-2013086248-A1 PHOTOCHROMIC MATERIALS THAT INCLUDE INDENO-FUSED NAPHTHOPYRANS PPG INDUSTRIES, INC. (US) 2013-06-13 WO disclosed
US-20120145973-A1 Photochromic Materials That Include Indeno-Fused Naphthopyrans TRANSITIONS OPTICAL INC. (US) 2012-06-14 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-20120145973-A1 Photochromic Materials That Include Indeno-Fused Naphthopyrans NQO1, INTS6, IPO4 LMNA 650/4885MAPT 2224/4885L3MBTL1 3391/4885

“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.