SCHEMBL17035192

SCHEMBL17035192

Cc1ccc2c(c1)Oc1cc(O)ccc1C21OC(=O)c2cc(C(C)C)ccc21

nearest known ligand 0.60

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
FTO Q9C0B1 10/20 0.60
MAPT P10636 4/20 0.60
HPGD P15428 2/20 0.60
MEN1 O00255 2/20 0.60
HTT P42858 2/20 0.60
KMT2A Q03164 2/20 0.60
CYP2C19 P33261 2/20 0.60
RECQL P46063 1/20 0.60
BLM P54132 1/20 0.60
SMAD3 P84022 1/20 0.60
PRMT1 Q99873 1/20 0.60
ACE2 Q9BYF1 1/20 0.60
TDP1 Q9NUW8 1/20 0.60
LMNA P02545 3/20 0.48
ALOX12 P18054 2/20 0.48
NPSR1 Q6W5P4 2/20 0.48
POLB P06746 1/20 0.48
GPR55 Q9Y2T6 1/20 0.48
ALDH1A1 P00352 2/20 0.44
CYP2C9 P11712 2/20 0.44

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
SCHEMBL20073857 0.94 FTO (0.67) FTOMAPTHPGDMEN1HTT
SCHEMBL19769261 0.93 FTO (0.48) FTOMAPTHPGDMEN1HTT
SCHEMBL4572038 0.88 FTO (0.72) FTOMAPTHPGDMEN1HTT
SCHEMBL18326523 0.86 FTO (0.79) FTOMAPTHPGDMEN1HTT
SCHEMBL21527330 0.86 FTO (0.66) FTOMAPTHPGDMEN1HTT
SCHEMBL12929974 0.85 MAPT (0.57) FTOMAPTHPGDMEN1HTT
SCHEMBL19769291 0.84 FTO (0.47) FTOMAPTHPGDMEN1HTT
SCHEMBL12863674 0.84 FTO (0.85) FTOMAPTHPGDMEN1HTT
SCHEMBL19224760 0.84 FTO (0.58) FTOMAPTHPGDMEN1HTT
SCHEMBL15496804 0.84 FTO (0.86) FTOMAPTHPGDMEN1HTT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12043674-B2 Synthetic cyclic peptides and methods of preparation and use thereof AUBURN UNIVERSITY (US) 2024-07-23 US disclosed
US-20180222916-A1 FUNCTIONALIZED NANOLUC INHIBITORS JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT 2018-08-09 US disclosed
US-20180104354-A1 CHIMERIC ANTIGEN RECEPTOR T CELL SWITCHES AND USES THEREOF THE SCRIPPS RESEARCH INSTITUTE 2018-04-19 US disclosed
US-20150238631-A1 CHIMERIC ANTIGEN RECEPTOR T CELL SWITCHES AND USES THEREOF THE CALIFORNIA INSTITUTE FOR BIOMEDICAL RESEARCH (US) 2015-08-27 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 (4 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-20180104354-A1 CHIMERIC ANTIGEN RECEPTOR T CELL SWITCHES AND USES THEREOF ICOS, HAVCR2, CD2 FTO 3696/4885MAPT 2599/4885HPGD 4238/4885
US-20150238631-A1 CHIMERIC ANTIGEN RECEPTOR T CELL SWITCHES AND USES THEREOF ICOS, HAVCR2, CD2 FTO 3696/4885MAPT 2599/4885HPGD 4238/4885
US-12043674-B2 Synthetic cyclic peptides and methods of preparation and use thereof VIP, PTMS, IAPP FTO 4813/4885MAPT 4013/4885HPGD 1136/4885
US-20180222916-A1 FUNCTIONALIZED NANOLUC INHIBITORS RNGTT, LUC7L2, GUSB FTO 2395/4885MAPT 4104/4885HPGD 1422/4885

“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.