SCHEMBL20935148

SCHEMBL20935148

CC(=O)O/N=C(\C)C(=O)c1ccc(Sc2ccc(C(=O)/C(C)=N/OC(C)=O)cc2)cc1

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
L3MBTL1 Q9Y468 3/20 0.50
HPGD P15428 3/20 0.50
LMNA P02545 2/20 0.50
KMT2A Q03164 2/20 0.48
ALDH1A1 P00352 2/20 0.44
MAPT P10636 4/20 0.38
SMN1; SMN2 Q16637 2/20 0.38
POLB P06746 1/20 0.38
PKM P14618 1/20 0.38
KDM4E B2RXH2 3/20 0.38
PTGIR P43119 1/20 0.37
CTSK P43235 1/20 0.35
CES2 O00748 2/20 0.33
CES1 P23141 2/20 0.33
ADRA2A P08913 1/20 0.32
ADRA2B P18089 1/20 0.32
ADRA2C P18825 1/20 0.32
RARB P10826 1/20 0.32
RARG P13631 1/20 0.32
RXRA P19793 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
SCHEMBL19795435 0.94 HPGD (0.56) L3MBTL1HPGDLMNAKMT2AALDH1A1
SCHEMBL19795439 0.94 L3MBTL1 (0.57) L3MBTL1HPGDLMNAKMT2AALDH1A1
SCHEMBL10075708 0.94 HPGD (0.44) L3MBTL1HPGDLMNAKMT2AALDH1A1
SCHEMBL10075752 0.94 LMNA (0.44) L3MBTL1HPGDLMNAKMT2AALDH1A1
SCHEMBL16019156 0.94 HPGD (0.56) L3MBTL1HPGDLMNAKMT2AALDH1A1
SCHEMBL24489413 0.94 L3MBTL1 (0.44) L3MBTL1HPGDLMNAKMT2AALDH1A1
SCHEMBL19751020 0.90 L3MBTL1 (0.41) L3MBTL1HPGDLMNAKMT2AALDH1A1
SCHEMBL10075710 0.87 L3MBTL1 (0.45) L3MBTL1HPGDLMNAKMT2AALDH1A1
SCHEMBL23550803 0.87 PARP10 (0.48) L3MBTL1HPGDLMNAKMT2AALDH1A1
SCHEMBL10075733 0.87 L3MBTL1 (0.39) L3MBTL1HPGDLMNAKMT2AALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230367052-A1 COLORING COMPOSITION, FILM, COLOR FILTER AND SOLID-STATE IMAGING ELEMENT FUJIFILM CORPORATION (JP) 2023-11-16 US disclosed
US-20230367052-A1 COLORING COMPOSITION, FILM, COLOR FILTER AND SOLID-STATE IMAGING ELEMENT FUJIFILM CORPORATION (JP) 2023-11-16 US disclosed
US-11639331-B2 Trans, trans-diketone oxime ester isomer, manufacturing method thereof and application thereof INSIGHT HIGH TECHNOLOGY CO., LTD (CN) 2023-05-02 US disclosed
US-11639331-B2 Trans, trans-diketone oxime ester isomer, manufacturing method thereof and application thereof INSIGHT HIGH TECHNOLOGY CO., LTD (CN) 2023-05-02 US disclosed
US-20210198193-A1 Trans, trans-diketone oxime ester isomer, manufacturing method thereof and application thereof INSIGHT HIGH TECH CO LTD (CN) 2021-07-01 US disclosed
WO-2019076145-A1 TRANS, TRANS-DIKETONE OXIME ESTER ISOMER, MANUFACTURING METHOD THEREFOR AND APPLICATION THEREOF 北京英力科技发展有限公司 2019-04-25 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 (2 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-20210198193-A1 Trans, trans-diketone oxime ester isomer, manufacturing method thereof and application thereof TKT, CYP51A1, TKFC L3MBTL1 2313/4885HPGD 866/4885LMNA 2370/4885
US-11639331-B2 Trans, trans-diketone oxime ester isomer, manufacturing method thereof and application thereof TKFC, TKT, CYP4F11 L3MBTL1 1952/4885HPGD 1011/4885LMNA 2424/4885

“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.