SCHEMBL9112042

SCHEMBL9112042

CC(C)c1ccc(CCCCCO)cc1

nearest known ligand 0.49

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA2 P00918 2/20 0.49
CYP4A11 Q02928 2/20 0.47
CYP4F2 P78329 1/20 0.47
S1PR1 P21453 1/20 0.46
S1PR3 Q99500 1/20 0.46
NPC1 O15118 1/20 0.43
RAB9A P51151 1/20 0.43
SMN1; SMN2 Q16637 1/20 0.43
ESR1 P03372 2/20 0.42
ADRA2A P08913 2/20 0.42
ADORA3 P0DMS8 2/20 0.42
TACR2 P21452 2/20 0.42
SLC6A2 P23975 2/20 0.42
SLC6A4 P31645 2/20 0.42
SLC6A3 Q01959 2/20 0.42
IDO1 P14902 2/20 0.42
ALDH1A1 P00352 2/20 0.42
KDM4E B2RXH2 1/20 0.42
LMNA P02545 1/20 0.42
SHBG P04278 1/20 0.42

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
SCHEMBL22918238 0.98 CYP4A11 (0.49) CA2CYP4A11CYP4F2S1PR1S1PR3
SCHEMBL11745515 0.92 CYP4A11 (0.47) CA2CYP4A11CYP4F2S1PR1S1PR3
SCHEMBL24074795 0.86 UCHL3 (0.44) CA2CYP4A11CYP4F2S1PR1S1PR3
SCHEMBL2222047 0.83 CA2 (0.52) CA2CYP4A11CYP4F2RAB9ASMN1; SMN2
Hydrogen Peroxide SCHEMBL9342704 0.83 CYP4A11 (0.41) CYP4A11CYP4F2S1PR1S1PR3NPC1
SCHEMBL9670730 0.82 CA2 (0.63) CA2CYP4A11CYP4F2ESR1ADRA2A
SCHEMBL3424786 0.82 CA2 (0.63) CA2CYP4A11CYP4F2ESR1ADRA2A
SCHEMBL31512262 0.82 CA2 (0.63) CA2CYP4A11CYP4F2ESR1ADRA2A
SCHEMBL23837668 0.82 CA2 (0.63) CA2CYP4A11CYP4F2ESR1ADRA2A
SCHEMBL4195590 0.82 CA2 (0.63) CA2CYP4A11CYP4F2ESR1ADRA2A

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-12030835-B2 Substituted amide compounds useful as farnesoid X receptor modulators BRISTOL-MYERS SQUIBB COMPANY (US) 2024-07-09 US disclosed
US-20220213026-A1 SUBSTITUTED AMIDE COMPOUNDS USEFUL AS FARNESOID X RECEPTOR MODULATORS BRISTOL MYERS SQUIBB CO (US) 2022-07-07 US disclosed
EP-0670831-A1 QUINOXALINE DERIVATIVE AS ANTIDIABETIC AGENT OTSUKA PHARMACEUTICAL CO., LTD. (JP) 1995-09-13 EP disclosed
WO-1995009159-A1 QUINOXALINE DERIVATIVE AS ANTIDIABETIC AGENT OTSUKA PHARMACEUTICAL COMPANY, LIMITED (JP) 1995-04-06 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 (2 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-20220213026-A1 SUBSTITUTED AMIDE COMPOUNDS USEFUL AS FARNESOID X RECEPTOR MODULATORS FXR1, NR1H4, FXR2 CA2 3365/4885CYP4A11 15/4885CYP4F2 111/4885
US-12030835-B2 Substituted amide compounds useful as farnesoid X receptor modulators FXR1, NR1H4, FXR2 CA2 3365/4885CYP4A11 15/4885CYP4F2 111/4885

“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.