SCHEMBL2018385

SCHEMBL2018385

CCCCCCc1cccc(CC(C)c2ccccc2O)c1CCCCCC

nearest known ligand 0.47

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 1/20 0.47
BID P55957 3/20 0.47
MCL1 Q07820 3/20 0.47
BCL2L1 Q07817 2/20 0.47
BAK1 Q16611 2/20 0.47
KAT8 Q9H7Z6 2/20 0.47
SAE1 Q9UBE0 2/20 0.47
PPARG P37231 1/20 0.47
PPARA Q07869 1/20 0.47
EP300 Q09472 1/20 0.47
KAT2A Q92830 1/20 0.47
KAT2B Q92831 1/20 0.47
KAT5 Q92993 1/20 0.47
CYSLTR2 Q9NS75 7/20 0.43
CYSLTR1 Q9Y271 7/20 0.43
LIPG Q9Y5X9 1/20 0.43
MMP2 P08253 2/20 0.41
F7 P08709 2/20 0.41
F3 P13726 2/20 0.41
KDM4E B2RXH2 1/20 0.41

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
SCHEMBL2022543 1.00 TSHR (0.47) TSHRBIDMCL1BCL2L1BAK1
SCHEMBL2018769 0.99 TSHR (0.49) TSHRBIDMCL1BCL2L1BAK1
SCHEMBL2026534 0.95 TSHR (0.50) TSHRBIDMCL1BCL2L1BAK1
SCHEMBL1845585 0.90 BID (0.45) BIDMCL1BCL2L1BAK1KAT8
SCHEMBL1841604 0.90 BID (0.45) BIDMCL1BCL2L1BAK1KAT8
SCHEMBL1954882 0.90 BID (0.47) TSHRBIDMCL1BCL2L1BAK1
SCHEMBL1955394 0.90 BID (0.47) TSHRBIDMCL1BCL2L1BAK1
SCHEMBL2023079 0.89 TSHR (0.53) TSHRBIDMCL1BCL2L1BAK1
SCHEMBL2024595 0.89 TSHR (0.53) TSHRBIDMCL1BCL2L1BAK1
SCHEMBL2019310 0.89 TSHR (0.53) TSHRBIDMCL1BCL2L1BAK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20110160476-A1 N-Substituted Carbamic Acid Ester Production Method and Isocyanate Production Method Using the N-Substituted Carbamic Acid Ester ASAHI KASEI CHEMICALS CORPORATION (JP) 2011-06-30 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 (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-20110160476-A1 N-Substituted Carbamic Acid Ester Production Method and Isocyanate Production Method Using the N-Substituted Carbamic Acid Ester ALKBH3, CPS1, APEH TSHR 2998/4885BID 2429/4885MCL1 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.