SCHEMBL7160653

SCHEMBL7160653

CCCCCCN(CCCCCC)CCC(C)C

nearest known ligand 0.47

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
PLA2G1B P04054 1/20 0.47
PLA2G2A P14555 1/20 0.47
DNM1 Q05193 5/20 0.44
TSHR P16473 1/20 0.38
THRB P10828 1/20 0.38
GGPS1 O95749 3/20 0.37
OPRM1 P35372 1/20 0.37
KDM5A P29375 2/20 0.37
PHF8 Q9UPP1 2/20 0.37
KDM4C Q9H3R0 1/20 0.37
KCNH2 Q12809 1/20 0.36
SPHK1 Q9NYA1 1/20 0.35
CA12 O43570 1/20 0.35
CA1 P00915 1/20 0.35
CA2 P00918 1/20 0.35
CA9 Q16790 1/20 0.35
LMNA P02545 1/20 0.34

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
SCHEMBL26673160 1.00 PLA2G1B (0.47) PLA2G1BPLA2G2ADNM1TSHRTHRB
SCHEMBL9785896 0.98 PLA2G1B (0.43) PLA2G1BPLA2G2ADNM1TSHRTHRB
SCHEMBL8938916 0.98 PLA2G1B (0.43) PLA2G1BPLA2G2ADNM1TSHRTHRB
SCHEMBL23228807 0.93 PLA2G1B (0.41) PLA2G1BPLA2G2ADNM1OPRM1KDM5A
SCHEMBL30929603 0.91 PLA2G1B (0.52) PLA2G1BPLA2G2ADNM1TSHRTHRB
SCHEMBL9245364 0.91 PLA2G1B (0.52) PLA2G1BPLA2G2ADNM1TSHRTHRB
SCHEMBL11756994 0.91 PLA2G1B (0.52) PLA2G1BPLA2G2ADNM1TSHRTHRB
SCHEMBL9252490 0.91 PLA2G1B (0.52) PLA2G1BPLA2G2ADNM1TSHRTHRB
SCHEMBL11785881 0.91 PLA2G1B (0.52) PLA2G1BPLA2G2ADNM1TSHRTHRB
SCHEMBL20445604 0.90 PLA2G1B (0.40) PLA2G1BPLA2G2ADNM1OPRM1KDM5A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9902985-B2 Chemoenzymatic methods for synthesizing moenomycin analogs PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 2018-02-27 US disclosed
US-9428438-B2 Process for preparing formic acid BASF SE (DE) 2016-08-30 US disclosed
EP-2925715-A1 METHOD FOR PRODUCING FORMIC ACID BASF SE (DE) 2015-10-07 EP disclosed
EP-2794539-B1 METHOD FOR PRODUCING FORMIC ACID BASF SE (DE) 2015-05-27 EP disclosed
US-20150119561-A1 CHEMOENZYMATIC METHODS FOR SYNTHESIZING MOENOMYCIN ANALOGS NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2015-04-30 US disclosed
US-20150079618-A1 METHODS AND COMPOUNDS FOR IDENTIFYING GLYCOSYLTRANSFERASE INHIBITORS PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 2015-03-19 US disclosed
US-8889905-B2 Process for preparing formic acid BASF SE (DE) 2014-11-18 US disclosed
EP-2794540-A1 PROCESS FOR PREPARING FORMIC ACID BASF SE (DE) 2014-10-29 EP disclosed
EP-2794539-A1 METHOD FOR PRODUCING FORMIC ACID BASF SE (DE) 2014-10-29 EP disclosed
US-8835683-B2 Process for preparing formic acid BASF SE (DE) 2014-09-16 US disclosed
WO-2014082845-A1 METHOD FOR PRODUCING FORMIC ACID BASF SE (DE) 2014-06-05 WO disclosed
US-20140148617-A1 PROCESS FOR PREPARING FORMIC ACID BASF SE (DE) 2014-05-29 US disclosed
US-20140018456-A1 PROCESS FOR PREPARING FORMIC ACID BASF SE (DE) 2014-01-16 US disclosed
US-20130190532-A1 PROCESS FOR PREPARING FORMIC ACID BASF SE (DE) 2013-07-25 US disclosed
WO-2013092403-A1 METHOD FOR PRODUCING FORMIC ACID BASF SE (DE) 2013-06-27 WO disclosed
WO-2013092157-A1 PROCESS FOR PREPARING FORMIC ACID BASF SE (DE) 2013-06-27 WO disclosed
US-20110136759-A1 MOENOMYCIN ANALOGS, METHODS OF SYNTHESIS, AND USES THEREOF NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2011-06-09 US disclosed
US-6576684-B1 Ammonium, phosphonium or sulfonium containing oligomers or polymers; controlled molecular weight, low polydispersity and a vinyl or dienyl end group; polymeric precursors and addi-tives CIBA SPECIALTY CHEMICALS CORPORATION 2003-06-10 US disclosed
EP-1112288-A1 THERMAL- AND PHOTOINITIATED RADICAL POLYMERIZATION IN THE PRESENCE OF AN ADDITION FRAGMENTATION AGENT Ciba SC Holding AG (CH) 2001-07-04 EP disclosed
WO-2000011041-A1 THERMAL- AND PHOTOINITIATED RADICAL POLYMERIZATION IN THE PRESENCE OF AN ADDITION FRAGMENTATION AGENT CIBA SPECIALTY CHEMICALS HOLDING INC. (CH) 2000-03-02 WO 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-20150119561-A1 CHEMOENZYMATIC METHODS FOR SYNTHESIZING MOENOMYCIN ANALOGS CYP51A1, COASY, MRM1 PLA2G1B 2672/4885PLA2G2A 2926/4885DNM1 492/4885
US-20140148617-A1 PROCESS FOR PREPARING FORMIC ACID MSMO1, FEN1, MED1 PLA2G1B 533/4885PLA2G2A 551/4885DNM1 136/4885
US-20140018456-A1 PROCESS FOR PREPARING FORMIC ACID F2, F5, FAH PLA2G1B 3150/4885PLA2G2A 3291/4885DNM1 2185/4885
US-20110136759-A1 MOENOMYCIN ANALOGS, METHODS OF SYNTHESIS, AND USES THEREOF MSN, MGAM, NISCH PLA2G1B 2204/4885PLA2G2A 2090/4885DNM1 96/4885
US-20130190532-A1 PROCESS FOR PREPARING FORMIC ACID F5, F12, ADH1A PLA2G1B 1701/4885PLA2G2A 2118/4885DNM1 1212/4885
US-20150079618-A1 METHODS AND COMPOUNDS FOR IDENTIFYING GLYCOSYLTRANSFERASE INHIBITORS MAGT1, GALNT1, NMT1 PLA2G1B 2602/4885PLA2G2A 2581/4885DNM1 1474/4885

“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.