SCHEMBL3212895

SCHEMBL3212895

CCC(=O)OC12CC3CC(CC(C3)C1)C2

nearest known ligand 0.50

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
CYP19A1 P11511 2/20 0.50
EPHX2 P34913 1/20 0.45
CYP17A1 P05093 1/20 0.45
NPSR1 Q6W5P4 3/20 0.43
TSHR P16473 1/20 0.43
NAAA Q02083 1/20 0.41
ALDH1A1 P00352 3/20 0.40
LMNA P02545 1/20 0.39
KMT2A Q03164 4/20 0.38
MEN1 O00255 3/20 0.38
SMN1; SMN2 Q16637 1/20 0.38
HTT P42858 1/20 0.38
L3MBTL1 Q9Y468 1/20 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
SCHEMBL2603076 0.86 NPSR1 (0.40) CYP19A1EPHX2CYP17A1NPSR1TSHR
SCHEMBL12251143 0.84 CYP19A1 (0.42) CYP19A1EPHX2CYP17A1NPSR1TSHR
SCHEMBL2603074 0.84 NPSR1 (0.63) CYP19A1EPHX2CYP17A1NPSR1TSHR
SCHEMBL12936719 0.84 EPHX2 (0.50) CYP19A1EPHX2CYP17A1NPSR1TSHR
SCHEMBL27436848 0.83 CYP19A1 (0.53) CYP19A1EPHX2CYP17A1NPSR1TSHR
SCHEMBL2603060 0.82 HSD11B1 (0.41) CYP19A1EPHX2CYP17A1NPSR1ALDH1A1
SCHEMBL14944490 0.82 DPP4 (0.40) CYP19A1EPHX2CYP17A1NPSR1TSHR
SCHEMBL27521122 0.81 CYP19A1 (0.45) CYP19A1EPHX2CYP17A1NPSR1TSHR
SCHEMBL12936716 0.81 EPHX2 (0.55) CYP19A1EPHX2CYP17A1NPSR1TSHR
SCHEMBL9917016 0.81 CYP19A1 (0.56) CYP19A1EPHX2CYP17A1NPSR1TSHR

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 86 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7473799-B2 Process for the preparation of synthetic retinoids with disubstituted adamantyl radical NANJING UNIVERSITY OF AERONAUTICS AND ASTRONAUTICS (CN) 2009-01-06 US claimed
US-20080108848-A1 Process for the preparation of synthetic retinoids with disubstituted adamantyl radical NANJING UNIVERSITY OF AERONAUTICS AND ASTRONAUTICS (CN) 2008-05-08 US claimed
US-7351521-B2 Photoresist composition for deep ultraviolet lithography AZ ELECTRONIC MATERIALS USA CORP. (US) 2008-04-01 US claimed
US-20070172762-A1 Photoresist composition for deep ultraviolet lithography DAMMEL RALPH R 2007-07-26 US claimed
US-20070154841-A1 Photoresist composition for deep ultraviolet lithography AZ ELECTRONIC MATERIALS USA CORP. 2007-07-05 US claimed
US-7211366-B2 Photoresist composition for deep ultraviolet lithography AZ ELECTRONIC MATERIALS USA CORP. (US) 2007-05-01 US claimed
EP-1602011-A2 PHOTORESIST COMPOSITION FOR DEEP ULTRAVIOLET LITHOGRAPHY AZ Electronic Materials USA Corp. (US) 2005-12-07 EP claimed
WO-2004074928-A2 PHOTORESIST COMPOSITION FOR DEEP ULTRAVIOLET LITHOGRAPHY AZ ELECTRONIC MATERIALS USA CORP. (US) 2004-09-02 WO claimed
US-20040166434-A1 Photoresist composition for deep ultraviolet lithography AZ ELECTRONIC MATERIALS USA CORP. 2004-08-26 US claimed
US-20040166433-A1 Photoresist composition for deep ultraviolet lithography AZ ELECTRONIC MATERIALS USA CORP. 2004-08-26 US claimed
EP-0358574-B1 PROCESS FOR THE PREPARATION OF ADAMANTANE-1 DERIVATIVES CENTRE INTERNATIONAL DE RECHERCHES DERMATOLOGIQUES GALDERMA - CIRD GALDERMA (FR) 1993-02-17 EP claimed
US-5015758-A Process for the preparation of 1-adamantane derivatives CENTRE INTERNATIONAL DE RECHERCHES DERMATOLOGIQUES (CIRD) (FR) 1991-05-14 US claimed
EP-0358574-A1 Process for the preparation of adamantane-1 derivatives CENTRE INTERNATIONAL DE RECHERCHES DERMATOLOGIQUES GALDERMA - CIRD GALDERMA (FR) 1990-03-14 EP claimed
EP-4658663-A2 PRODRUGS OF 4'-SUBSTITUTED NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS Merck Sharp & Dohme LLC (US) 2025-12-10 EP disclosed
US-20240287124-A1 PRODRUGS OF 4'-SUBSTITUTED NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS MERCK SHARP & DOHME LLC (US) 2024-08-29 US disclosed
WO-2024163262-A2 PRODRUGS OF 4'-SUBSTITUTED NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS MERCK SHARP & DOHME LLC (US) 2024-08-08 WO disclosed
CN-1881084-A Chemically amplified resist material and pattern formation method using the same MATSUSHITA ELECTRIC INDUSTRIAL CO LTD (JP) 2006-12-20 CN disclosed
EP-0358574-B1 PROCESS FOR THE PREPARATION OF ADAMANTANE-1 DERIVATIVES CENTRE INTERNATIONAL DE RECHERCHES DERMATOLOGIQUES GALDERMA - CIRD GALDERMA (FR) 1993-02-17 EP disclosed
US-5015758-A Process for the preparation of 1-adamantane derivatives CENTRE INTERNATIONAL DE RECHERCHES DERMATOLOGIQUES (CIRD) (FR) 1991-05-14 US disclosed
EP-0358574-A1 Process for the preparation of adamantane-1 derivatives CENTRE INTERNATIONAL DE RECHERCHES DERMATOLOGIQUES GALDERMA - CIRD GALDERMA (FR) 1990-03-14 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 (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-20240287124-A1 PRODRUGS OF 4'-SUBSTITUTED NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS DNTT, NAPRT, NAMPT CYP19A1 761/4885EPHX2 1430/4885CYP17A1 1125/4885
US-20080108848-A1 Process for the preparation of synthetic retinoids with disubstituted adamantyl radical RXRA, RARA, RXRB CYP19A1 301/4885EPHX2 1219/4885CYP17A1 471/4885

“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.