SCHEMBL1365559

SCHEMBL1365559

Cc1ccc(S(=O)(=O)O)cc1.NCCCCCCC(=O)OCc1ccccc1

nearest known ligand 0.61

Known targets — ChEMBL curated mechanism

ABL1BMXBRAFBTKCHRNA4CHRNB2CSNK1EEGFRERBB2F10FLT1FLT3FLT4IGF1RINSRITKJAK3KDRKITOPRM1PARP1PARP2PDGFRBPIK3CDRAF1RETSLC18A2TECTXKdacAdacBdacCftsImrcAmrcBmrdArplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of None. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
LMNA P02545 2/20 0.61
ALDH1A1 P00352 7/20 0.47
GAA P10253 1/20 0.47
CYP1A2 P05177 1/20 0.46
CYP2C9 P11712 1/20 0.46
MAPT P10636 1/20 0.46
KMT2A Q03164 2/20 0.45
RAB9A P51151 1/20 0.43
EPHX2 P34913 1/20 0.42
CA1 P00915 1/20 0.42
CA2 P00918 1/20 0.42
MAPK1 P28482 2/20 0.41
TDP1 Q9NUW8 1/20 0.41
L3MBTL1 Q9Y468 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
SCHEMBL1365966 1.00 LMNA (0.61) LMNAALDH1A1GAACYP1A2CYP2C9
SCHEMBL30689605 1.00 LMNA (0.61) LMNAALDH1A1GAACYP1A2CYP2C9
SCHEMBL1365332 1.00 LMNA (0.61) LMNAALDH1A1GAACYP1A2CYP2C9
SCHEMBL1365851 0.99 LMNA (0.62) LMNAALDH1A1GAACYP1A2CYP2C9
SCHEMBL1363911 0.95 LMNA (0.64) LMNAALDH1A1GAACYP1A2CYP2C9
SCHEMBL717926 0.92 LMNA (0.68) LMNAALDH1A1GAACYP1A2CYP2C9
SCHEMBL18281078 0.92 LMNA (0.68) LMNAALDH1A1GAACYP1A2CYP2C9
SCHEMBL7801225 0.86 LMNA (0.50) LMNAALDH1A1GAACYP1A2CYP2C9
SCHEMBL57630 0.85 LMNA (0.62) LMNAALDH1A1GAACYP1A2CYP2C9
SCHEMBL1177430 0.85 LMNA (0.62) LMNAALDH1A1GAACYP1A2CYP2C9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1644323-B1 HISTONE DEACETYLASE INHIBITORS AND METHODS OF USE THEREOF UNIV GEORGETOWN (US) 2015-03-18 EP disclosed
EP-2258677-B1 HISTONE DEACETYLASE INHIBITORS UNIV GEORGETOWN (US) 2014-06-18 EP disclosed
US-8748463-B2 Histone deacetylase inhibitors and methods of use thereof GEORGETOWN UNIVERSITY (US) 2014-06-10 US disclosed
US-20130065963-A1 Histone Deacetylase Inhibitors and Methods of Use Thereof GEORGETOWN UNIVERSITY (US) 2013-03-14 US disclosed
US-8222451-B2 Histone deacetylase inhibitors and methods of use thereof GEORGETOWN UNIVERSITY (US) 2012-07-17 US disclosed
US-8067600-B2 Histone deacetylase inhibitors and methods of use thereof GEORGETOWN UNIVERSITY (US) 2011-11-29 US disclosed
US-20110098504-A1 Histone Deacetylase Inhibitors and Methods of Use Thereof GEORGETOWN UNIVERSITY (US) 2011-04-28 US disclosed
EP-2258677-A2 Histone deacetylase inhibitors and methods of use thereof GEORGETOWN UNIVERSITY (US) 2010-12-08 EP disclosed
US-7842835-B2 Histone deacetylase inhibitors and methods of use thereof GEORGETOWN UNIVERSITY (US) 2010-11-30 US disclosed
US-20090163543-A1 Histone Deacetylase Inhibitors and Methods of Use Thereof GEORGETOWN UNIVERSITY (US) 2009-06-25 US disclosed
US-7507828-B2 Histone deacetylase inhibitors and methods of use thereof GEORGETOWN UNIVERSITY (US) 2009-03-24 US disclosed
EP-1644323-A4 HISTONE DEACETYLASE INHIBITORS AND METHODS OF USE THEREOF UNIV GEORGETOWN (US) 2007-06-20 EP disclosed
US-7186797-B2 Polypeptide conjugates with extended circulating half-lives EPIX PHARMACEUTICALS, INC. (US) 2007-03-06 US disclosed
EP-1644323-A2 HISTONE DEACETYLASE INHIBITORS AND METHODS OF USE THEREOF GEORGETOWN UNIVERSITY (US) 2006-04-12 EP disclosed
US-20050032831-A1 Histone deacetylase inhibitors and methods of use thereof GEORGETOWN UNIVERSITY 2005-02-10 US disclosed
WO-2005007091-A2 HISTONE DEACETYLASE INHIBITORS AND METHODS OF USE THEREOF GEORGETOWN UNIVERSITY (US) 2005-01-27 WO disclosed
US-20050014839-A1 Histone deacetylase inhibitors and methods of use thereof GEORGETOWN UNIVERSITY 2005-01-20 US disclosed
US-20040254119-A1 Polypeptide conjugates with extended circulating half-lives EPIX PHARMACEUTICALS, INC. 2004-12-16 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 (6 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-20130065963-A1 Histone Deacetylase Inhibitors and Methods of Use Thereof HDAC5, HDAC6, HDAC1 LMNA 1947/4885ALDH1A1 437/4885GAA 120/4885
US-20090163543-A1 Histone Deacetylase Inhibitors and Methods of Use Thereof HDAC5, HDAC6, HDAC1 LMNA 2137/4885ALDH1A1 376/4885GAA 123/4885
US-20050032831-A1 Histone deacetylase inhibitors and methods of use thereof HDAC5, HDAC6, HDAC1 LMNA 2137/4885ALDH1A1 376/4885GAA 123/4885
US-20110098504-A1 Histone Deacetylase Inhibitors and Methods of Use Thereof HDAC5, HDAC6, HDAC1 LMNA 1947/4885ALDH1A1 437/4885GAA 120/4885
US-20050014839-A1 Histone deacetylase inhibitors and methods of use thereof HDAC5, HDAC6, HDAC1 LMNA 1947/4885ALDH1A1 437/4885GAA 120/4885
US-20040254119-A1 Polypeptide conjugates with extended circulating half-lives ALB, TTR, SHBG LMNA 2670/4885ALDH1A1 2791/4885GAA 741/4885

“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.