SCHEMBL2225542

SCHEMBL2225542

CC(C)(C)c1cc(P(Cl)c2cc(C(C)(C)C)cc(C(C)(C)C)c2)cc(C(C)(C)C)c1

nearest known ligand 0.46

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
GABRA1 P14867 1/20 0.46
GABRB2 P47870 1/20 0.46
POLB P06746 1/20 0.37
KDM4E B2RXH2 1/20 0.34
GAA P10253 1/20 0.34
MAPT P10636 1/20 0.34
RXRA P19793 2/20 0.32
RXRB P28702 2/20 0.32
RXRG P48443 2/20 0.32
HTR1D P28221 1/20 0.32
ALDH1A1 P00352 1/20 0.31
HPGD P15428 1/20 0.31
ALOX15 P16050 1/20 0.31
HSD17B10 Q99714 1/20 0.31
TDP1 Q9NUW8 1/20 0.31
TSHR P16473 1/20 0.31
CYP2C19 P33261 1/20 0.30

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
SCHEMBL2154614 0.77 HDAC8 (0.42) GAAMAPTRXRARXRBALDH1A1
SCHEMBL93161 0.76 GABRA1 (0.69) GABRA1GABRB2POLBKDM4EGAA
SCHEMBL19998396 0.76 GABRA1 (0.48) GABRA1GABRB2POLBKDM4EGAA
SCHEMBL2154563 0.74 TSHR (0.48) POLBMAPTALDH1A1HPGDALOX15
SCHEMBL16694547 0.74 GABRA1 (0.46) GABRA1GABRB2POLBKDM4EGAA
SCHEMBL497733 0.74 CES2 (0.41) MAPTRXRARXRBRXRGALDH1A1
SCHEMBL1305213 0.74 GABRA1 (0.46) GABRA1GABRB2POLBKDM4EGAA
SCHEMBL1305235 0.74 GABRA1 (0.46) GABRA1GABRB2POLBKDM4EGAA
SCHEMBL10394690 0.73 GABRA1 (0.65) GABRA1GABRB2POLBKDM4EGAA
SCHEMBL10415675 0.73 GABRA1 (0.65) GABRA1GABRB2POLBKDM4EGAA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1598053-B1 Use of a composition containing at least one phosphine as majority reducing agent to remove the artificial colour of keratinic fibres OREAL (FR) 2006-12-20 EP claimed
EP-1598053-A1 Use of a composition containing at least one phosphine as majority reducing agent to remove the artificial colour of keratinic fibres L'OREAL (FR) 2005-11-23 EP claimed
US-20050251928-A1 Method for stripping artificial color from keratin fibers L'OREAL (FR) 2005-11-17 US claimed
CN-114426560-B Chiral diphosphine ligand, rhodium complex thereof, preparation method and application thereof 南开沧州渤海新区绿色化工研究有限公司 2024-11-05 CN disclosed
US-20230165771-A1 PROCESS FOR TREATING KERATIN FIBERS USING PARTICULAR AMINO ACIDS IN HIGH CONCENTRATION L'OREAL (FR) 2023-06-01 US disclosed
EP-4171490-A1 PROCESS FOR TREATING KERATIN FIBERS USING PARTICULAR AMINO ACIDS IN HIGH CONCENTRATION L'OREAL (FR) 2023-05-03 EP disclosed
CN-115996701-A Method for treating keratin fibres using a high concentration of a specific amino acid 莱雅公司 2023-04-21 CN disclosed
WO-2022003040-A1 PROCESS FOR TREATING KERATIN FIBERS USING PARTICULAR AMINO ACIDS IN HIGH CONCENTRATION L'OREAL (FR) 2022-01-06 WO disclosed
CN-108774271-A A kind of chiral nitrogen nitrogen phosphine tridentate ligand and its application based on ferrocene frame having ferrocene frame 浙江工业大学 2018-11-09 CN disclosed
WO-2017025244-A1 COSMETIC PROCESS FOR TREATING KERATIN MATERIALS L'OREAL (FR) 2017-02-16 WO disclosed
WO-2017018498-A1 COMPOSITION, PROCESS, METHOD AND USE FOR KERATIN FIBERS L'OREAL (FR) 2017-02-02 WO disclosed
US-20150166479-A1 PROCESS FOR SYNTHESIS OF EZETIMIBE AND INTERMEDIATES USED IN SAID PROCESS SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY, CHINESE ACADEMY OF SCIENCES (CN) 2015-06-18 US disclosed
EP-2876102-A1 PROCESS FOR SYNTHESIS OF EZETIMIBE AND INTERMEDIATES USED IN SAID PROCESS Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences (CN) 2015-05-27 EP disclosed
US-20130224830-A1 EGGSHELL MEMBRANE SOLUBILIZATION METHOD USING ENZYMES AMANO ENZYME INC. (JP) 2013-08-29 US disclosed
EP-2612922-A1 EGGSHELL MEMBRANE SOLUBILIZATION METHOD USING ENZYMES Amano Enzyme Inc. (JP) 2013-07-10 EP disclosed
WO-2011089985-A1 COSMETIC COMPOSITION FOR KERATIN FIBERS L'OREAL (FR) 2011-07-28 WO disclosed
EP-1598053-B1 Use of a composition containing at least one phosphine as majority reducing agent to remove the artificial colour of keratinic fibres OREAL (FR) 2006-12-20 EP disclosed
EP-1598053-A1 Use of a composition containing at least one phosphine as majority reducing agent to remove the artificial colour of keratinic fibres L'OREAL (FR) 2005-11-23 EP disclosed
US-20050251928-A1 Method for stripping artificial color from keratin fibers L'OREAL (FR) 2005-11-17 US disclosed
US-6084133-A REACTING A PHOSPHINE HALIDE WITH A METAL, THEN PROTONATION RESULTING DIORGANO-SUBSTITUTED METAL PHOSPHIDE; SIMPLIFICATION, NONTOXIC, EFFICIENCY KANKYO KAGAKU CENTER CO., LTD. (JP) 2000-07-04 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-20150166479-A1 PROCESS FOR SYNTHESIS OF EZETIMIBE AND INTERMEDIATES USED IN SAID PROCESS HMGCR, COASY, APOB GABRA1 2601/4885GABRB2 2776/4885POLB 699/4885
US-20230165771-A1 PROCESS FOR TREATING KERATIN FIBERS USING PARTICULAR AMINO ACIDS IN HIGH CONCENTRATION KRT18, CKAP4, VIM GABRA1 3720/4885GABRB2 3624/4885POLB 2406/4885
US-20050251928-A1 Method for stripping artificial color from keratin fibers KRT18, DSG1, JUP GABRA1 4394/4885GABRB2 4249/4885POLB 2208/4885

“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.