SCHEMBL20211883

SCHEMBL20211883

CC(C)(C)OC(=O)CC[C@@H](C(N)=O)N1Cc2cc(N3CCN(C(=O)OC(C)(C)C)CC3)ccc2C1=O

nearest known ligand 0.42

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PDK2 Q15119 1/20 0.42
MAPT P10636 3/20 0.42
LMNA P02545 2/20 0.42
ALDH1A1 P00352 2/20 0.42
NAMPT P43490 1/20 0.40
MEN1 O00255 5/20 0.39
KMT2A Q03164 5/20 0.39
GPR119 Q8TDV5 3/20 0.39
NPSR1 Q6W5P4 2/20 0.39
SMN1; SMN2 Q16637 3/20 0.37
CYP2C19 P33261 1/20 0.37
HTT P42858 1/20 0.37
DDB1 Q16531 1/20 0.37
CRBN Q96SW2 1/20 0.37
MMP2 P08253 1/20 0.36
MMP13 P45452 1/20 0.36
MMP14 P50281 1/20 0.36
ADAMTS5 Q9UNA0 1/20 0.36
TLR9 Q9NR96 1/20 0.36
TLR7 Q9NYK1 1/20 0.36

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
SCHEMBL30517962 1.00 PDK2 (0.42) PDK2MAPTLMNAALDH1A1NAMPT
SCHEMBL20211885 1.00 PDK2 (0.42) PDK2MAPTLMNAALDH1A1NAMPT
SCHEMBL30612712 1.00 PDK2 (0.42) PDK2MAPTLMNAALDH1A1NAMPT
SCHEMBL20231940 1.00 PDK2 (0.42) PDK2MAPTLMNAALDH1A1NAMPT
SCHEMBL25095190 0.95 PDK2 (0.41) PDK2MAPTLMNAALDH1A1NAMPT
SCHEMBL31554733 0.93 PDK2 (0.42) PDK2MAPTLMNAALDH1A1NAMPT
SCHEMBL23038660 0.93 ALOX15 (0.35) PDK2MAPTLMNAALDH1A1NAMPT
SCHEMBL23038659 0.93 ALOX15 (0.35) PDK2MAPTLMNAALDH1A1NAMPT
SCHEMBL27081249 0.93 ALOX15 (0.35) PDK2MAPTLMNAALDH1A1NAMPT
SCHEMBL27301527 0.91 GABRA1 (0.39) PDK2MAPTALDH1A1MEN1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260098027-A1 PHARMACEUTICALLY ACCEPTABLE SALT AND CRYSTAL FORM OF TETRAHYDRONAPHTHALENE DERIVATIVE, AND PREPARATION METHOD JIANGSU HENGRUI PHARMACEUTICALS CO LTD (CN) 2026-04-09 US disclosed
EP-4699660-A2 METHODS OF TREATING BREAST CANCER WITH TETRAHYDRONAPHTHALENE DERIVATIVES AS ESTROGEN RECEPTOR DEGRADERS Arvinas Operations, Inc. (US) 2026-02-25 EP disclosed
EP-4021450-B1 METHODS OF TREATING BREAST CANCER WITH TETRAHYDRONAPHTHALENE DERIVATIVES AS ESTROGEN RECEPTOR DEGRADERS ARVINAS OPERATIONS INC (US) 2025-11-05 EP disclosed
US-20250320195-A1 TETRAHYDRONAPHTHALENE AND TETRAHYDROISOQUINOLINE DERIVATIVES AS ESTROGEN RECEPTOR DEGRADERS ARVINAS OPERATIONS INC (US) 2025-10-16 US disclosed
EP-4596538-A1 PHARMACEUTICALLY ACCEPTABLE SALT AND CRYSTAL FORM OF TETRAHYDRONAPHTHALENE DERIVATIVE, AND PREPARATION METHOD Jiangsu Hengrui Pharmaceuticals Co., Ltd. (CN) 2025-08-06 EP disclosed
US-20250144230-A1 LINKERS FOR USE IN ANTIBODY DRUG CONJUGATES ORUM THERAPEUTICS, INC. (KR) 2025-05-08 US disclosed
US-20250120968-A1 METHODS OF TREATING BREAST CANCER WITH TETRAHYDRONAPHTHALENE DERIVATIVES AS ESTROGEN RECEPTOR DEGRADERS ARVINAS OPERATIONS, INC. 2025-04-17 US disclosed
EP-4501327-A2 SUBSTITUTED PYRROLOPYRIMIDINE AND PYRAZOLOPYRIMIDINE AS BRUTON S TYROSINEKINASE (BTK) DEGRADERS Accutar Biotechnology Inc. (US) 2025-02-05 EP disclosed
US-12208095-B2 Methods of treating breast cancer with tetrahydronaphthalene derivatives as estrogen receptor degraders ARVINAS OPERATIONS, INC. (US) 2025-01-28 US disclosed
US-12172981-B2 Tetrahydronaphthalene and tetrahydroisoquinoline derivatives as estrogen receptor degraders ARVINAS OPERATIONS, INC. (US) 2024-12-24 US disclosed
CN-111454248-A Tetrahydronaphthalene and tetrahydroisoquinoline derivatives as estrogen receptor degraders 阿尔维纳斯运营股份有限公司 2020-07-28 CN disclosed
EP-3675839-A1 NOVEL COMPOUNDS HAVING ESTROGEN RECEPTOR ALPHA DEGRADATION ACTIVITY AND USES THEREOF Accutar Biotechnology Inc. (US) 2020-07-08 EP disclosed
US-10696659-B2 Compounds having estrogen receptor alpha degradation activity and uses thereof ACCUTAR BIOTECHNOLOGY INC. (US) 2020-06-30 US disclosed
US-20200157078-A1 NOVEL COMPOUNDS HAVING ESTROGEN RECEPTOR ALPHA DEGRADATION ACTIVITY AND USES THEREOF ACCUTAR BIOTECHNOLOGY INC. (US) 2020-05-21 US disclosed
US-20200157078-A1 NOVEL COMPOUNDS HAVING ESTROGEN RECEPTOR ALPHA DEGRADATION ACTIVITY AND USES THEREOF ACCUTAR BIOTECHNOLOGY INC. (US) 2020-05-21 US disclosed
US-10647698-B2 Tetrahydronaphthalene and tetrahydroisoquinoline derivatives as estrogen receptor degraders ARVINAS OPERATIONS, INC. (US) 2020-05-12 US disclosed
US-10647698-B2 Tetrahydronaphthalene and tetrahydroisoquinoline derivatives as estrogen receptor degraders ARVINAS OPERATIONS, INC. (US) 2020-05-12 US disclosed
US-20180155322-A1 TETRAHYDRONAPHTHALENE AND TETRAHYDROISOQUINOLINE DERIVATIVES AS ESTROGEN RECEPTOR DEGRADERS ARVINAS OPERATIONS, INC. 2018-06-07 US disclosed
US-20180155322-A1 TETRAHYDRONAPHTHALENE AND TETRAHYDROISOQUINOLINE DERIVATIVES AS ESTROGEN RECEPTOR DEGRADERS ARVINAS OPERATIONS, INC. 2018-06-07 US disclosed
WO-2018102725-A1 TETRAHYDRONAPHTHALENE AND TETRAHYDROISOQUINOLINE DERIVATIVES AS ESTROGEN RECEPTOR DEGRADERS Arvinas, Inc. (US) 2018-06-07 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 (10 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-20260098027-A1 PHARMACEUTICALLY ACCEPTABLE SALT AND CRYSTAL FORM OF TETRAHYDRONAPHTHALENE DERIVATIVE, AND PREPARATION METHOD MDH2, MDH1, GOT1 PDK2 100/4885MAPT 1017/4885LMNA 3851/4885
US-12172981-B2 Tetrahydronaphthalene and tetrahydroisoquinoline derivatives as estrogen receptor degraders MDM2, CRBN, VHL PDK2 2447/4885MAPT 2558/4885LMNA 2706/4885
US-20200157078-A1 NOVEL COMPOUNDS HAVING ESTROGEN RECEPTOR ALPHA DEGRADATION ACTIVITY AND USES THEREOF ESR2, ESRRG, ESR1 PDK2 1292/4885MAPT 4353/4885LMNA 1951/4885
US-12208095-B2 Methods of treating breast cancer with tetrahydronaphthalene derivatives as estrogen receptor degraders ESR1, GPER1, ESR2 PDK2 2718/4885MAPT 1516/4885LMNA 2660/4885
US-20250320195-A1 TETRAHYDRONAPHTHALENE AND TETRAHYDROISOQUINOLINE DERIVATIVES AS ESTROGEN RECEPTOR DEGRADERS MDM2, CRBN, VHL PDK2 2447/4885MAPT 2558/4885LMNA 2706/4885
US-20250120968-A1 METHODS OF TREATING BREAST CANCER WITH TETRAHYDRONAPHTHALENE DERIVATIVES AS ESTROGEN RECEPTOR DEGRADERS ESR1, GPER1, ESR2 PDK2 2718/4885MAPT 1516/4885LMNA 2660/4885
US-20180155322-A1 TETRAHYDRONAPHTHALENE AND TETRAHYDROISOQUINOLINE DERIVATIVES AS ESTROGEN RECEPTOR DEGRADERS MDM2, CRBN, VHL PDK2 2447/4885MAPT 2558/4885LMNA 2706/4885
US-10696659-B2 Compounds having estrogen receptor alpha degradation activity and uses thereof ESR2, ESRRG, ESR1 PDK2 1433/4885MAPT 4446/4885LMNA 1529/4885
US-20250144230-A1 LINKERS FOR USE IN ANTIBODY DRUG CONJUGATES CD2BP2, CD47, EPCAM PDK2 3020/4885MAPT 432/4885LMNA 2657/4885
US-10647698-B2 Tetrahydronaphthalene and tetrahydroisoquinoline derivatives as estrogen receptor degraders MDM2, CRBN, VHL PDK2 2447/4885MAPT 2558/4885LMNA 2706/4885

“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.