SCHEMBL3617692

SCHEMBL3617692

CCC(O)C(C)C1OC1CC(C)/C=C/C=C(\C)C1OC(=O)CC(O)CCC2(CO2)C(OC(C)=O)/C=C/C1C

nearest known ligand 0.68

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SF3B3 Q15393 10/20 0.68
HMGCR P04035 2/20 0.32
MEN1 O00255 2/20 0.30
KMT2A Q03164 2/20 0.30
SMN1; SMN2 Q16637 2/20 0.30
LMNA P02545 2/20 0.30
CYP3A4 P08684 2/20 0.30
TSHR P16473 2/20 0.30
ABCB11 O95342 1/20 0.30
ALDH1A1 P00352 1/20 0.30
MAPK1 P28482 1/20 0.30
MTOR P42345 1/20 0.30
HTT P42858 1/20 0.30
NPSR1 Q6W5P4 1/20 0.30
GMNN O75496 1/20 0.30
TP53 P04637 1/20 0.30
CYP1A2 P05177 1/20 0.30
CYP2D6 P10635 1/20 0.30
NFKB1 P19838 1/20 0.30
BLM P54132 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
SCHEMBL13748880 0.93 SF3B3 (0.71) SF3B3HMGCRMEN1KMT2ASMN1; SMN2
SCHEMBL14539614 0.92 SF3B3 (0.76) SF3B3HMGCRMEN1KMT2ASMN1; SMN2
SCHEMBL12877318 0.92 SF3B3 (0.76) SF3B3HMGCRMEN1KMT2ASMN1; SMN2
SCHEMBL12877481 0.92 SF3B3 (0.76) SF3B3HMGCRMEN1KMT2ASMN1; SMN2
SCHEMBL905749 0.92 SF3B3 (0.76) SF3B3HMGCRMEN1KMT2ASMN1; SMN2
SCHEMBL30311586 0.92 SF3B3 (0.76) SF3B3HMGCRMEN1KMT2ASMN1; SMN2
SCHEMBL1505041 0.91 SF3B3 (0.69) SF3B3HMGCRMEN1KMT2ASMN1; SMN2
SCHEMBL12833633 0.91 SF3B3 (0.69) SF3B3HMGCRMEN1KMT2ASMN1; SMN2
SCHEMBL13503195 0.91 SF3B3 (0.68) SF3B3HMGCR
SCHEMBL3626331 0.91 SF3B3 (0.68) SF3B3HMGCR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7655442-B2 Efficiently producing a macrolide compound, in which a cyclodextrin is made to be present in a culture broth of actinomycetes; antitumor agents EISAI R&D MANAGEMENT CO., LTD. (JP) 2010-02-02 US claimed
US-20070155696-A1 Method for stabilizing macrolide compounds MERCIAN CORPORATION (JP) 2007-07-05 US claimed
EP-1710244-A1 METHOD OF STABILIZING MACROLIDE COMPOUND Eisai R&D Management Co., Ltd. (JP) 2006-10-11 EP claimed
US-7026352-B1 Physiologically active substances MERCIAN CORPORATION (JP) 2006-04-11 US claimed
US-7667052-B2 Bioactive substance EISAI R&D MANAGEMENT CO., LTD. (JP) 2010-02-23 US disclosed
US-7667052-B2 Bioactive substance EISAI R&D MANAGEMENT CO., LTD. (JP) 2010-02-23 US disclosed
US-7655442-B2 Efficiently producing a macrolide compound, in which a cyclodextrin is made to be present in a culture broth of actinomycetes; antitumor agents EISAI R&D MANAGEMENT CO., LTD. (JP) 2010-02-02 US disclosed
US-20070155696-A1 Method for stabilizing macrolide compounds MERCIAN CORPORATION (JP) 2007-07-05 US disclosed
EP-1710244-A1 METHOD OF STABILIZING MACROLIDE COMPOUND Eisai R&D Management Co., Ltd. (JP) 2006-10-11 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 (1 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-20070155696-A1 Method for stabilizing macrolide compounds MRPL21, ERG28, RPN1 SF3B3 2845/4885HMGCR 173/4885MEN1 2937/4885

“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.