SCHEMBL8396014

SCHEMBL8396014

CC12CCC(=O)C=C1C=CC1C2CCC2(C)C1CC[C@H]2CCC(=O)O

nearest known ligand 0.66

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PGR P06401 3/20 0.66
CYP3A4 P08684 3/20 0.66
ALDH1A1 P00352 3/20 0.66
CYP2C19 P33261 1/20 0.66
AR P10275 1/20 0.66
CHRM1 P11229 1/20 0.66
TBXA2R P21731 1/20 0.66
ADRA1A P35348 1/20 0.66
CYP19A1 P11511 6/20 0.57
TDP1 Q9NUW8 2/20 0.55
NR3C1 P04150 2/20 0.55
LMNA P02545 2/20 0.55
PDE4D Q08499 1/20 0.55
CHRM2 P08172 1/20 0.51
OPRK1 P41145 1/20 0.51
MEN1 O00255 1/20 0.51
KMT2A Q03164 1/20 0.51
SRD5A2 P31213 2/20 0.43
CYP17A1 P05093 1/20 0.40
SMN1; SMN2 Q16637 2/20 0.38

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
SCHEMBL11326826 1.00 PGR (0.66) PGRCYP3A4ALDH1A1CYP2C19AR
SCHEMBL19628769 1.00 PGR (0.66) PGRCYP3A4ALDH1A1CYP2C19AR
SCHEMBL17889177 0.92 AR (0.62) PGRCYP3A4ALDH1A1CYP2C19AR
SCHEMBL6843336 0.90 PGR (0.69) PGRCYP3A4ALDH1A1CYP2C19AR
SCHEMBL6843333 0.90 PGR (0.69) PGRCYP3A4ALDH1A1CYP2C19AR
SCHEMBL23638424 0.89 PGR (0.67) PGRCYP3A4ALDH1A1CYP2C19AR
SCHEMBL19625822 0.89 PGR (0.67) PGRCYP3A4ALDH1A1CYP2C19AR
SCHEMBL19625918 0.89 PGR (0.67) PGRCYP3A4ALDH1A1CYP2C19AR
SCHEMBL29891105 0.87 PGR (0.64) PGRCYP3A4ALDH1A1CYP2C19AR
SCHEMBL23514168 0.86 PGR (0.64) PGRCYP3A4ALDH1A1CYP2C19AR

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-20090325918-A1 Synthesis and separation of optically active isomers and cyclopropyl derivatives of spironolactone and their biological action SOMBERG JOHN C 2009-12-31 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-20090325918-A1 Synthesis and separation of optically active isomers and cyclopropyl derivatives of spironolactone and their biological action HSD17B7, CYP17A1, HSD17B11 PGR 79/4885CYP3A4 372/4885ALDH1A1 2056/4885

“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.