SCHEMBL5962393

SCHEMBL5962393

CC(C)N(C)[C@H](C)[C@@H](O)c1ccccc1

nearest known ligand 0.70

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 2/20 0.70
ALDH1A1 P00352 2/20 0.70
AOC3 Q16853 5/20 0.66
GAA P10253 1/20 0.53
ADRA2C P18825 2/20 0.52
ADRA2A P08913 1/20 0.52
LMNA P02545 1/20 0.52
HIF1A Q16665 1/20 0.52
CHRM2 P08172 1/20 0.48
ADRA1A P35348 1/20 0.48
RGS12 O14924 1/20 0.48
GLA P06280 1/20 0.48
CYP3A4 P08684 1/20 0.48
CYP2D6 P10635 1/20 0.48
CYP2C9 P11712 1/20 0.48
PKM P14618 1/20 0.48
ALOX15 P16050 1/20 0.48
TSHR P16473 1/20 0.48
ALOX12 P18054 1/20 0.48
NFKB1 P19838 1/20 0.48

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
SCHEMBL5962400 1.00 KDM4E (0.70) KDM4EALDH1A1AOC3GAAADRA2C
SCHEMBL13741557 1.00 KDM4E (0.70) KDM4EALDH1A1AOC3GAAADRA2C
SCHEMBL3874299 1.00 KDM4E (0.70) KDM4EALDH1A1AOC3GAAADRA2C
SCHEMBL10108616 1.00 KDM4E (0.70) KDM4EALDH1A1AOC3GAAADRA2C
SCHEMBL12322302 0.85 KDM4E (0.73) KDM4EALDH1A1AOC3GAAADRA2C
SCHEMBL18091009 0.85 KDM4E (0.73) KDM4EALDH1A1AOC3GAAADRA2C
Methylephedrine SCHEMBL99673 0.83 KDM4E (1.00) KDM4EALDH1A1AOC3GAAADRA2C
Methylephedrine SCHEMBL11959977 0.83 KDM4E (1.00) KDM4EALDH1A1AOC3GAAADRA2C
Methylephedrine SCHEMBL2712293 0.83 KDM4E (1.00) KDM4EALDH1A1AOC3GAAADRA2C
Methylephedrine SCHEMBL99674 0.83 KDM4E (1.00) KDM4EALDH1A1AOC3GAAADRA2C

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0593917-A1 Process for the preparation of optically active esters and thioesters FIRMENICH SA (CH) 1994-04-27 EP claimed
US-10172821-B2 Histone deacetylase inhibitors President & Fellows of Harvard College Dana-Farber Cancer Institute, Inc. (US) 2019-01-08 US disclosed
US-20170360740-A1 HISTONE DEACETYLASE INHIBITORS DANA-FARBER CANCER INSTITUTE, INC. 2017-12-21 US disclosed
US-20170360740-A1 HISTONE DEACETYLASE INHIBITORS DANA-FARBER CANCER INSTITUTE, INC. 2017-12-21 US disclosed
US-9724321-B2 Histone deacetylase inhibitors PRESIDENT & FELLOWS OF HARVARD COLLEGE (US) 2017-08-08 US disclosed
US-9724321-B2 Histone deacetylase inhibitors PRESIDENT & FELLOWS OF HARVARD COLLEGE (US) 2017-08-08 US disclosed
US-20160143874-A1 HISTONE DEACETYLASE INHIBITORS DANA-FARBER CANCER INSTITUTE, INC. 2016-05-26 US disclosed
US-9199923-B2 Histone deacetylase inhibitors PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 2015-12-01 US disclosed
US-20150038581-A1 HISTONE DEACETYLASE INHIBITORS Harvard University & Medical School 2015-02-05 US disclosed
US-20140213620-A1 HISTONE DEACETYLASE INHIBITORS BRADNER JAMES ELLIOT (US) 2014-07-31 US disclosed
US-20090312363-A1 BIFUNCTIONAL HISTONE DEACETYLASE INHIBITORS PRESIDENT AND FELLOWS OF HARVARD COLLEGE 2009-12-17 US disclosed
EP-1910261-B1 SUBSTITUTED CYCLOHEXANONES FIRMENICH & CIE (CH) 2009-11-11 EP disclosed
US-20090209590-A1 Histone Deacetylase and Tubulin Deacetylase Inhibitors PRESIDENT AND FELLOWS OF HARVARD COLLEGE 2009-08-20 US disclosed
US-7470820-B2 Substituted cyclohexanones FIRMENICH SA (CH) 2008-12-30 US disclosed
US-20080269245-A1 Dioxanes and uses thereof PRESIDENT AND FELLOWS OF HARVARD COLLEGE 2008-10-30 US disclosed
US-20080228008-A1 Substituted Cyclohexanones FIRMENICH SA (CH) 2008-09-18 US disclosed
US-7244853-B2 Dioxanes and uses thereof PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 2007-07-17 US disclosed
US-7244853-B2 Dioxanes and uses thereof PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 2007-07-17 US disclosed
WO-2007010483-A1 SUBSTITUTED CYCLOHEXANONES FIRMENICH SA (CH) 2007-01-25 WO disclosed
US-20040072849-A1 Dioxanes and uses thereof NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2004-04-15 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 (10 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-20140213620-A1 HISTONE DEACETYLASE INHIBITORS HDAC1, HDAC11, HDAC7 KDM4E 172/4885ALDH1A1 764/4885AOC3 2541/4885
US-20160143874-A1 HISTONE DEACETYLASE INHIBITORS HDAC1, HDAC11, HDAC7 KDM4E 154/4885ALDH1A1 955/4885AOC3 3195/4885
US-20090312363-A1 BIFUNCTIONAL HISTONE DEACETYLASE INHIBITORS HDAC1, HDAC11, HDAC2 KDM4E 209/4885ALDH1A1 786/4885AOC3 3901/4885
US-20090209590-A1 Histone Deacetylase and Tubulin Deacetylase Inhibitors HDAC6, HDAC1, HDAC5 KDM4E 2003/4885ALDH1A1 320/4885AOC3 3599/4885
US-20170360740-A1 HISTONE DEACETYLASE INHIBITORS HDAC1, HDAC11, HDAC7 KDM4E 172/4885ALDH1A1 764/4885AOC3 2541/4885
US-20040072849-A1 Dioxanes and uses thereof UTS2R, HDAC5, AMDHD2 KDM4E 164/4885ALDH1A1 682/4885AOC3 2471/4885
US-20080228008-A1 Substituted Cyclohexanones NQO1, CYP2J2, CBR3 KDM4E 1219/4885ALDH1A1 388/4885AOC3 1084/4885
US-20150038581-A1 HISTONE DEACETYLASE INHIBITORS HDAC1, HDAC11, HDAC7 KDM4E 172/4885ALDH1A1 764/4885AOC3 2541/4885
US-20080269245-A1 Dioxanes and uses thereof UTS2R, MAN2B2, AMDHD2 KDM4E 130/4885ALDH1A1 750/4885AOC3 2322/4885
US-10172821-B2 Histone deacetylase inhibitors HDAC1, HDAC11, HDAC7 KDM4E 172/4885ALDH1A1 764/4885AOC3 2541/4885

“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.