SCHEMBL3555946

SCHEMBL3555946

C=C(B1OC(C)(C)C(C)(C)O1)c1ccccc1

nearest known ligand 0.41

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LPL P06858 2/20 0.40
LIPG Q9Y5X9 2/20 0.40
ANPEP P15144 1/20 0.40
LAP3 P28838 1/20 0.40
P4HB P07237 1/20 0.39
F2 P00734 1/20 0.35
PRSS1 P07477 1/20 0.35
APLNR P35414 1/20 0.34
MAOA P21397 5/20 0.33
MAOB P27338 5/20 0.33
SMN1; SMN2 Q16637 2/20 0.33
MAPT P10636 2/20 0.33
MEN1 O00255 1/20 0.33
KMT2A Q03164 1/20 0.33
LMNA P02545 1/20 0.33
XBP1 P17861 1/20 0.33
ATM Q13315 1/20 0.33
NPSR1 Q6W5P4 1/20 0.33
HTT P42858 1/20 0.33
ALDH1A1 P00352 1/20 0.33

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
SCHEMBL31408750 0.89 LIPG (0.51) LPLLIPGANPEPLAP3SMN1; SMN2
SCHEMBL18471018 0.82 ALDH1A1 (0.35) APLNRSMN1; SMN2MEN1KMT2ALMNA
SCHEMBL25172268 0.81 LMNA (0.36) APLNRMAOAMAOBKMT2ALMNA
SCHEMBL6236173 0.79 LPL (0.42) LPLLIPGANPEPLAP3P4HB
SCHEMBL6236171 0.79 LPL (0.42) LPLLIPGANPEPLAP3P4HB
SCHEMBL6236165 0.79 LPL (0.42) LPLLIPGANPEPLAP3P4HB
SCHEMBL17226547 0.79 LPL (0.45) LPLLIPGF2PRSS1SMN1; SMN2
SCHEMBL31408747 0.79 C1S (0.40) SMN1; SMN2MEN1KMT2AATMNPSR1
SCHEMBL30502749 0.79 CES2 (0.42) MAOAMAOBSMN1; SMN2MEN1KMT2A
SCHEMBL25168903 0.79 CES2 (0.42) MAOAMAOBSMN1; SMN2MEN1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260055113-A1 HETEROARYL COMPOUNDS FOR THE TREATMENT OF CANCER HOFFMANN-LA ROCHE INC. (US) 2026-02-26 US disclosed
EP-4313981-B1 3,4-DIHYDRO-2,7-NAPHTHYRIDINE-1,6(2H,7H)-DIONES AS MEK INHIBITORS PFIZER (US) 2026-02-25 EP disclosed
EP-4688751-A1 ANTIVIRAL HETEROCYCLIC COMPOUNDS Enanta Pharmaceuticals, Inc. (US) 2026-02-11 EP disclosed
US-20250368659-A1 Antiviral Heterocyclic Compounds ENANTA PHARM INC (US) 2025-12-04 US disclosed
US-12428403-B2 N-(heterocyclyl and heterocyclylalkyl)-3-benzylpyridin-2-amine derivatives as SSTR4 agonists TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2025-09-30 US disclosed
US-20250263411-A1 3,4-DIHYDRO-2,7-NAPHTHYRIDINE-1,6(2H,7H)-DIONES AS MEK INHIBITORS PFIZER INC. (US) 2025-08-21 US disclosed
US-12358921-B2 Antiviral heterocyclic compounds ENANTA PHARMACEUTICALS, INC. (US) 2025-07-15 US disclosed
EP-4568965-A1 HETEROARYL COMPOUNDS FOR THE TREATMENT OF CANCER F. Hoffmann-La Roche AG (CH) 2025-06-18 EP disclosed
WO-2025111414-A1 TRPM3-MODULATING BENZOFURAN DERIVATIVES KATHOLIEKE UNIVERSITEIT LEUVEN (BE) 2025-05-30 WO disclosed
US-20250084074-A1 SUBSTITUTED HETEROCYCLES AS HSET INHIBITORS MERCK PATENT GMBH (DE) 2025-03-13 US disclosed
EP-1963312-B1 BETA-SECRETASE MODULATORS AND METHODS OF USE AMGEN INC (US) 2014-07-02 EP disclosed
EP-2748149-A1 PYRIDAZINONE COMPOUNDS AND THEIR USE AS DAAO INHIBITORS Takeda Pharmaceutical Company Limited (JP) 2014-07-02 EP disclosed
US-20140179680-A1 Substituted Imidazopyridines as HDM2 Inhibitors MERCK SHARP & DOHME LLC 2014-06-26 US disclosed
WO-2014100065-A1 SUBSTITUTED IMIDAZOPYRIDINES AS HDM2 INHIBITORS MERCK SHARP & DOHME CORP. (US) 2014-06-26 WO disclosed
US-20130052281-A1 NOVEL COMPOUNDS TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2013-02-28 US disclosed
WO-2013027000-A1 PYRIDAZINONE COMPOUNDS AND THEIR USE AS DAAO INHIBITORS TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2013-02-28 WO disclosed
US-7838676-B2 Beta-secretase modulators and methods of use AMGEN INC. (US) 2010-11-23 US disclosed
EP-1963312-A1 BETA-SECRETASE MODULATORS AND METHODS OF USE Amgen Inc. (US) 2008-09-03 EP disclosed
US-20070173521-A1 Beta-secretase modulators and methods of use AMGEN INC. 2007-07-26 US disclosed
WO-2007061930-A1 BETA-SECRETASE MODULATORS AND METHODS OF USE AMGEN INC. (US) 2007-05-31 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 (9 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-20260055113-A1 HETEROARYL COMPOUNDS FOR THE TREATMENT OF CANCER H4C1; H4C2; H4C3; H4C4; H4C5; H4C6; H4C8; H4C9; H4C11; H4C12; H4C13; H4C14; H4C15; H4C16, HCCS, CLIC1 LPL 2073/4885LIPG 2834/4885ANPEP 2838/4885
US-20140179680-A1 Substituted Imidazopyridines as HDM2 Inhibitors DDX21, ING2, MDM2 LPL 4183/4885LIPG 3961/4885ANPEP 2054/4885
US-20130052281-A1 NOVEL COMPOUNDS ABCG2, F12, UGT1A1 LPL 2106/4885LIPG 3053/4885ANPEP 3103/4885
US-20250084074-A1 SUBSTITUTED HETEROCYCLES AS HSET INHIBITORS VHL, CDKN1A, CCNI LPL 3897/4885LIPG 2743/4885ANPEP 2654/4885
US-12428403-B2 N-(heterocyclyl and heterocyclylalkyl)-3-benzylpyridin-2-amine derivatives as SSTR4 agonists SSTR4, SSTR3, SSTR1 LPL 3062/4885LIPG 2292/4885ANPEP 1469/4885
US-12358921-B2 Antiviral heterocyclic compounds ACE, HPRT1, ACE2 LPL 2002/4885LIPG 2271/4885ANPEP 310/4885
US-20250263411-A1 3,4-DIHYDRO-2,7-NAPHTHYRIDINE-1,6(2H,7H)-DIONES AS MEK INHIBITORS NRAS, KRAS, BRAF LPL 4871/4885LIPG 3592/4885ANPEP 2813/4885
US-20070173521-A1 Beta-secretase modulators and methods of use BACE1, BACE2, APP LPL 1183/4885LIPG 1471/4885ANPEP 106/4885
US-20250368659-A1 Antiviral Heterocyclic Compounds ACE, HPRT1, ACE2 LPL 2002/4885LIPG 2271/4885ANPEP 310/4885

“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.