SCHEMBL4466762

SCHEMBL4466762

CC(=O)c1cc(O)c(C)c(C)c1O

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 3/20 0.52
KMT2A Q03164 3/20 0.52
KDM4E B2RXH2 3/20 0.52
MAPT P10636 2/20 0.52
NSD2 O96028 1/20 0.52
POLB P06746 1/20 0.52
MCL1 Q07820 1/20 0.52
SMN1; SMN2 Q16637 2/20 0.41
ALOX15 P16050 1/20 0.41
ALOX12 P18054 1/20 0.41
HTT P42858 2/20 0.41
ACHE P22303 1/20 0.39
CYP3A4 P08684 3/20 0.38
HPGD P15428 2/20 0.38
ALDH1A1 P00352 1/20 0.38
MAPK1 P28482 1/20 0.38
CYP2C9 P11712 1/20 0.37
CYP2C19 P33261 1/20 0.37
TDP1 Q9NUW8 1/20 0.37
L3MBTL1 Q9Y468 1/20 0.37

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
SCHEMBL12178198 0.86 MEN1 (0.52) MEN1KMT2AKDM4EMAPTNSD2
SCHEMBL6901292 0.84 SMN1; SMN2 (0.48) MEN1KMT2AKDM4EMAPTNSD2
SCHEMBL11083912 0.82 THRB (0.48) MEN1KMT2AKDM4EMAPTMCL1
SCHEMBL13912812 0.82 MEN1 (0.47) MEN1KMT2AKDM4EMAPTNSD2
SCHEMBL14753933 0.78 MEN1 (0.40) MEN1KMT2AKDM4EMAPTNSD2
SCHEMBL30931542 0.77 MEN1 (0.42) MEN1KMT2AKDM4EMAPTNSD2
SCHEMBL30931541 0.77 MEN1 (0.42) MEN1KMT2AKDM4EMAPTNSD2
SCHEMBL12803161 0.77 ACHE (0.39) MEN1KMT2AKDM4EMAPTNSD2
SCHEMBL5838618 0.77 HSD17B10 (0.50) MEN1KMT2AKDM4EMAPTPOLB
SCHEMBL10498460 0.76 MEN1 (0.55) MEN1KMT2AKDM4EMAPTNSD2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9981935-B2 Formation of chiral 4-chromanones using chiral pyrrolidines in the presence of acids DSM IP ASSETS B.V. (NL) 2018-05-29 US disclosed
EP-3016939-B1 FORMATION OF CHIRAL 4-CHROMANONES USING CHIRAL PYRROLIDINES IN THE PRESENCE OF ACIDS DSM IP ASSETS BV (NL) 2017-03-29 EP disclosed
US-20160168110-A1 FORMATION OF CHIRAL 4-CHROMANONES USING CHIRAL PYRROLIDINES IN THE PRESENCE OF ACIDS DSM IP ASSETS B.V. (NL) 2016-06-16 US disclosed
EP-3016939-A1 FORMATION OF CHIRAL 4-CHROMANONES USING CHIRAL PYRROLIDINES IN THE PRESENCE OF ACIDS DSM IP Assets B.V. (NL) 2016-05-11 EP disclosed
WO-2015001027-A1 FORMATION OF CHIRAL 4-CHROMANONES USING CHIRAL PYRROLIDINES IN THE PRESENCE OF ACIDS DSM IP ASSETS B.V. (NL) 2015-01-08 WO disclosed
US-20140031388-A1 AKT INACTIVATION BY TOCOPHERYL DERIVATIVES CHEN CHING-SHIH (US) 2014-01-30 US disclosed
EP-2100963-B1 METHOD OF VITAMIN PRODUCTION DCV INC (US) 2011-12-14 EP disclosed
EP-2100963-A1 Method of vitamin production DCV Inc. doing business as Bio-Technical Resourses (US) 2009-09-16 EP disclosed
US-7576094-B2 Spiro derivatives as lipoxygenase inhibitors ELI LILLY AND COMPANY (US) 2009-08-18 US disclosed
EP-1836183-A2 SPIRO DERIVATIVES AS LIPOXYGENASE INHIBITORS Galileo Pharmaceuticals, Inc. (US) 2007-09-26 EP disclosed
EP-1095034-A1 PREPARATION OF TOCOPHEROLS EASTMAN CHEMICAL COMPANY (US) 2001-05-02 EP disclosed
WO-2000001649-A1 METHOD OF VITAMIN PRODUCTION DCV, INC. DOING BUSINESS AS BIO-TECHNICAL RESOURCES (US) 2000-01-13 WO disclosed
WO-2000001685-A1 PREPARATION OF TOCOPHEROLS EASTMAN CHEMICAL COMPANY (US) 2000-01-13 WO disclosed
US-5318993-A Antihyperlipidemic benzoquinones BRISTOL-MYERS SQUIBB COMPANY (US) 1994-06-07 US disclosed
EP-0443710-B1 Benzoquinone antiallergy and antiinflammatory agents PFIZER (US) 1994-05-11 EP disclosed
US-5104874-A Cyclooxygenase and lipoxygenase inhibitob PFIZER INC. (US) 1992-04-14 US disclosed
EP-0443710-A1 Benzoquinone antiallergy and antiinflammatory agents PFIZER INC. (US) 1991-08-28 EP disclosed
EP-0038092-B1 PHOTOGRAPHIC MATERIAL SUITED FOR USE IN DIFFUSION TRANSFER PHOTOGRAPHY AGFA-GEVAERT N.V. (BE) 1984-03-07 EP disclosed
US-4371604-A Photographic material suited for use in diffusion transfer photography AGFA-GEVAERT, N.V. (BE) 1983-02-01 US disclosed
EP-0038092-A1 Photographic material suited for use in diffusion transfer photography AGFA-GEVAERT N.V. (BE) 1981-10-21 EP 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-20160168110-A1 FORMATION OF CHIRAL 4-CHROMANONES USING CHIRAL PYRROLIDINES IN THE PRESENCE OF ACIDS CROCC, CBR3, HCCS MEN1 3257/4885KMT2A 4391/4885KDM4E 3168/4885
US-20140031388-A1 AKT INACTIVATION BY TOCOPHERYL DERIVATIVES AKT3, OXSR1, PIK3R1 MEN1 4546/4885KMT2A 3346/4885KDM4E 830/4885

“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.