SCHEMBL5158684

SCHEMBL5158684

COC1=C(O)C(=O)C(C)=C(C)C1=O

nearest known ligand 0.42

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
DUSP3 P51452 1/20 0.42
CDC25A P30304 2/20 0.41
CDC25B P30305 2/20 0.41
APEX1 P27695 6/20 0.41
MAPT P10636 5/20 0.40
TDP1 Q9NUW8 3/20 0.40
LMNA P02545 3/20 0.40
CYP2C19 P33261 3/20 0.40
CYP3A4 P08684 2/20 0.40
CYP2D6 P10635 2/20 0.40
CYP2C9 P11712 2/20 0.40
MAPK1 P28482 2/20 0.40
PGR P06401 1/20 0.40
MAOA P21397 1/20 0.40
TBXA2R P21731 1/20 0.40
AVPR2 P30518 1/20 0.40
HTR2B P41595 1/20 0.40
HTT P42858 1/20 0.40
PDE3A Q14432 1/20 0.40
SIRT2 Q8IXJ6 1/20 0.40

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
SCHEMBL33978 0.88 DUSP3 (0.52) DUSP3CDC25ACDC25BAPEX1MAPT
SCHEMBL9175352 0.84 MAPT (0.42) DUSP3CDC25ACDC25BAPEX1MAPT
SCHEMBL21727072 0.81 MAPT (0.44) DUSP3CDC25ACDC25BAPEX1MAPT
Aurantiogliocladin SCHEMBL487583 0.81 MAPT (0.50) DUSP3CDC25ACDC25BAPEX1MAPT
SCHEMBL9180312 0.80 DUSP3 (0.48) DUSP3CDC25ACDC25BAPEX1MAPT
SCHEMBL12592463 0.76 CDC25A (0.58) DUSP3CDC25ACDC25BAPEX1MAPT
SCHEMBL9655485 0.75 CDC25A (0.64) DUSP3CDC25ACDC25BAPEX1MAPT
SCHEMBL10609498 0.74 DUSP3 (0.58) DUSP3MAPTTDP1LMNACYP2C19
SCHEMBL5818650 0.71 MAPT (0.38) DUSP3CDC25ACDC25BMAPTTDP1
SCHEMBL24925731 0.70 MAPT (0.44) APEX1MAPTTDP1LMNACYP2C19

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20070130702-A1 Dyeing process using a specific compound containing active methylene and a compound chosen from a specific aldehyde, a specific ketone, a quinone and a diiminoisoindoline or 3-aminoisoindolone derivative L'OREAL S.A. 2007-06-14 US claimed
US-6635090-B1 Dyeing method using a specific cationic derivative and a compound selected among a specific aldehyde, a specific ketone, a quinone and a di-imino-isoindoline or 3-amino-isoindolone derivative L'OREAL, S.A. (FR) 2003-10-21 US claimed
US-6458168-B1 Hair dyeing method using an aliphatic cationic amine and compound chosen from an aldehyde, a ketone, a quinone, a di-imino-isoindoline, and a 3-aminoisoindolone derivative L'OREAL S.A. (FR) 2002-10-01 US claimed
US-6451067-B1 HAIR DYE MIXTURE L'OREAL S.A. (FR) 2002-09-17 US claimed
EP-3843696-B1 PROCESS AND COMPOSITION FOR COLORING KERATIN FIBERS OREAL (FR) 2025-04-09 EP disclosed
CN-113164346-B Composition for keratin fibres comprising a direct dye 莱雅公司 2024-04-16 CN disclosed
CN-112601515-B Method and composition for coloring keratin fibers 莱雅公司 2024-04-05 CN disclosed
WO-2024048429-A1 COSMETIC PROCESS USING PARTICLE WITH MICROPROTRUSION L'OREAL (FR) 2024-03-07 WO disclosed
WO-2023228870-A1 COMPOSITION FOR COLORING KERATIN FIBERS L'OREAL (FR) 2023-11-30 WO disclosed
US-11672743-B2 Composition for keratin fibers comprising a direct dye L'OREAL (FR) 2023-06-13 US disclosed
US-20230051189-A1 COSMETIC PROCESS USING MICRONEEDLE SHEET L'OREAL (FR) 2023-02-16 US disclosed
US-11540992-B2 Process and composition for coloring keratin fibers L'OREAL (FR) 2023-01-03 US disclosed
EP-1056435-A1 DYEING METHOD USING AN ALIPHATIC CATIONIC AMINE AND A ALDEHYDE OR KETONE OR QUINONE OR DI-IMINO-ISOINDOLINE OR 3-AMINO-ISOINDOLONE DERIVATIVES L'OREAL (FR) 2000-12-06 EP disclosed
WO-2000038639-A1 DYEING METHOD USING A SPECIFIC CATIONIC DERIVATIVE AND A COMPOUND SELECTED AMONG A SPECIFIC ALDEHYDE, A SPECIFIC KETONE, A QUINONE AND A DI-IMINO-ISOINDOLINE OR 3-AMINO-ISOINDOLONE DERIVATIVE L'OREAL (FR) 2000-07-06 WO disclosed
WO-2000038640-A1 HAIR DYEING METHOD USING AN ALIPHATIC CATIONIC AMINE AND A ALDEHYDE OR KETONE OR QUINONE OR DI-IMINO-ISOINDOLINE OR 3-AMINO-ISO-INDOLONE DERIVATIVES L'OREAL (FR) 2000-07-06 WO disclosed
WO-2000038641-A1 DYEING METHOD USING AN ALIPHATIC CATIONIC AMINE AND A ALDEHYDE OR KETONE OR QUINONE OR DI-IMINO-ISOINDOLINE OR 3-AMINO-ISOINDOLONE DERIVATIVES L'OREAL (FR) 2000-07-06 WO disclosed
EP-0659397-B1 Process for direct coloration of human keratinic fibers by natural dyes and water steam OREAL (FR) 1999-04-14 EP disclosed
US-5725603-A Process for the direct dying of keratinous fibres using natural dyes and water vapor L'OREAL (FR) 1998-03-10 US disclosed
EP-0659397-A1 Process for direct coloration of human keratinic fibers by natural dyes and water steam L'OREAL (FR) 1995-06-28 EP disclosed
US-4867751-A HAIR DYES L'OREAL (FR) 1989-09-19 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 (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-20070130702-A1 Dyeing process using a specific compound containing active methylene and a compound chosen from a specific aldehyde, a specific ketone, a quinone and a diiminoisoindoline or 3-aminoisoindolone derivative KRT18, NDUFB5, NDUFB7 DUSP3 3863/4885CDC25A 3521/4885CDC25B 3174/4885
US-11540992-B2 Process and composition for coloring keratin fibers KRT18, PRKDC, KIF5C DUSP3 2471/4885CDC25A 1604/4885CDC25B 1357/4885
US-11672743-B2 Composition for keratin fibers comprising a direct dye KRT18, MKI67, DSG1 DUSP3 4088/4885CDC25A 4093/4885CDC25B 3638/4885

“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.