SCHEMBL30720114

SCHEMBL30720114

CC(C)(C)OC(=O)N1CCN(c2ccc(C(=O)NC3CCC(=O)NC3=O)nc2)CC1

nearest known ligand 0.63

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
CRBN Q96SW2 11/20 0.63
DDB1 Q16531 10/20 0.63
SMN1; SMN2 Q16637 2/20 0.52
MEN1 O00255 1/20 0.52
MAPT P10636 1/20 0.52
TSHR P16473 1/20 0.52
KMT2A Q03164 1/20 0.52
USP30 Q70CQ3 2/20 0.44
GPR119 Q8TDV5 3/20 0.43
WNT3A P56704 1/20 0.42
HTT P42858 1/20 0.41
NPSR1 Q6W5P4 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
SCHEMBL27238864 1.00 CRBN (0.63) CRBNDDB1SMN1; SMN2MEN1MAPT
SCHEMBL27260521 1.00 CRBN (0.63) CRBNDDB1SMN1; SMN2MEN1MAPT
SCHEMBL24481327 0.94 CRBN (0.58) CRBNDDB1SMN1; SMN2MEN1MAPT
SCHEMBL29579057 0.94 CRBN (0.58) CRBNDDB1SMN1; SMN2MEN1MAPT
SCHEMBL25631540 0.93 CRBN (0.55) CRBNDDB1SMN1; SMN2MEN1MAPT
SCHEMBL29265208 0.92 CRBN (0.54) CRBNDDB1SMN1; SMN2MEN1MAPT
SCHEMBL30602899 0.88 CRBN (0.52) CRBNDDB1SMN1; SMN2MEN1MAPT
SCHEMBL29578814 0.88 CRBN (0.52) CRBNDDB1SMN1; SMN2MEN1MAPT
SCHEMBL30965772 0.88 DDB1 (0.76) CRBNDDB1SMN1; SMN2MEN1MAPT
SCHEMBL30965775 0.88 DDB1 (0.76) CRBNDDB1SMN1; SMN2MEN1MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260028354-A1 TETRAHYDRONAPHTHALENE DERIVATIVES AS ESTROGEN RECEPTOR DEGRADERS REGENT OF THE UNIV OF MICHIGAN (US) 2026-01-29 US disclosed
US-20260007681-A1 INDOLE DERIVATIVES AS ESTROGEN RECEPTOR DEGRADERS UNIV MICHIGAN (US) 2026-01-08 US disclosed
US-20260000676-A1 CHROMAN DERIVATIVES AS ESTROGEN RECEPTOR DEGRADERS UNIV MICHIGAN REGENTS (US) 2026-01-01 US disclosed
EP-4554948-A1 TETRAHYDRONAPHTHALENE DERIVATIVES AS ESTROGEN RECEPTOR DEGRADERS Regents of the University of Michigan (US) 2025-05-21 EP disclosed
WO-2024015409-A1 CHROMAN DERIVATIVES AS ESTROGEN RECEPTOR DEGRADERS REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2024-01-18 WO disclosed
WO-2024015406-A1 INDOLE DERIVATIVES AS ESTROGEN RECEPTOR DEGRADERS REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2024-01-18 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 (3 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-20260028354-A1 TETRAHYDRONAPHTHALENE DERIVATIVES AS ESTROGEN RECEPTOR DEGRADERS ESRRA, ESR2, ESRRB CRBN 524/4885DDB1 1861/4885SMN1; SMN2 2810/4885
US-20260000676-A1 CHROMAN DERIVATIVES AS ESTROGEN RECEPTOR DEGRADERS ESRRA, ESR2, ESRRB CRBN 347/4885DDB1 2218/4885SMN1; SMN2 2280/4885
US-20260007681-A1 INDOLE DERIVATIVES AS ESTROGEN RECEPTOR DEGRADERS ESRRA, ESR2, AR CRBN 570/4885DDB1 2677/4885SMN1; SMN2 3411/4885

“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.