SCHEMBL7109323

SCHEMBL7109323

CC(C)c1[c]c(C(C)C)cc(C(=O)CCc2c(C(C)C)cc(C(C)C)cc2C(C)C)c1

nearest known ligand 0.39

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
FABP3 P05413 2/20 0.39
FABP4 P15090 2/20 0.39
USP5 P45974 1/20 0.36
FABP5 Q01469 1/20 0.35
SOAT2 O75908 1/20 0.33
MYC P01106 1/20 0.33
SOAT1 P35610 1/20 0.33
MAP2K3 P46734 1/20 0.33
GABRA1 P14867 1/20 0.33
GABRB2 P47870 1/20 0.33
GAA P10253 1/20 0.30
MEN1 O00255 1/20 0.30
KMT2A Q03164 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
SCHEMBL7206928 0.85 FABP3 (0.41) FABP3FABP4USP5FABP5SOAT2
SCHEMBL7109320 0.78 FABP3 (0.35) FABP3FABP4FABP5SOAT2MYC
SCHEMBL8706658 0.77 FABP3 (0.46) FABP3FABP4FABP5GABRA1GABRB2
SCHEMBL27986389 0.76 FABP3 (0.50) FABP3FABP4USP5FABP5SOAT2
SCHEMBL7206870 0.76 SRD5A2 (0.39) FABP3FABP4FABP5SOAT2MYC
SCHEMBL8495463 0.75 FABP3 (0.53) FABP3FABP4USP5FABP5SOAT2
SCHEMBL7211116 0.74 RAB9A (0.51) GAAMEN1KMT2A
SCHEMBL7108814 0.71 FABP3 (0.41) FABP3FABP4FABP5GABRA1GABRB2
SCHEMBL7206347 0.71 GABRA1 (0.43) SOAT2MYCSOAT1MAP2K3GABRA1
SCHEMBL7207694 0.70 HSD17B3 (0.50) MEN1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20030134898-A1 Dual inhibitors of wax ester and cholesteryl ester synthesis for inhibiting sebum production HOMAN REYNOLD (US) 2003-07-17 US claimed
EP-0841913-B1 USE OF SULFAMIC ACID DERIVATIVES, ACYL SULFONAMIDES OR SULFONYL CARBAMATES FOR THE MANUFACTURE OF A MEDICAMENT FOR LOWERING LIPOPROTEIN LEVELS WARNER LAMBERT CO (US) 2003-02-05 EP claimed
EP-1281399-A2 Dual inhibitors of wax ester and cholesteryl ester synthesis for inhibiting sebum production WARNER-LAMBERT COMPANY (US) 2003-02-05 EP claimed
US-20030134898-A1 Dual inhibitors of wax ester and cholesteryl ester synthesis for inhibiting sebum production HOMAN REYNOLD (US) 2003-07-17 US disclosed
EP-1281399-A2 Dual inhibitors of wax ester and cholesteryl ester synthesis for inhibiting sebum production WARNER-LAMBERT COMPANY (US) 2003-02-05 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-20030134898-A1 Dual inhibitors of wax ester and cholesteryl ester synthesis for inhibiting sebum production ACAT2, LCAT, SOAT1 FABP3 1591/4885FABP4 250/4885USP5 1930/4885

“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.