SCHEMBL5371487

SCHEMBL5371487

O=C1c2ccccc2C(=O)N1CCOCCOCCO

nearest known ligand 0.79

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 3/20 0.54
GAA P10253 1/20 0.51
HPGD P15428 2/20 0.51
NPSR1 Q6W5P4 1/20 0.51
RAB9A P51151 6/20 0.50
NPC1 O15118 3/20 0.50
MEN1 O00255 2/20 0.50
KMT2A Q03164 2/20 0.50
TSHR P16473 1/20 0.50
MAPT P10636 1/20 0.50
GLA P06280 1/20 0.49
BRCA1 P38398 1/20 0.49
GLS O94925 1/20 0.49
ALDH1A1 P00352 1/20 0.48
LMNA P02545 1/20 0.48
HEXA P06865 1/20 0.47
HEXB P07686 1/20 0.47
CASP3 P42574 1/20 0.47
SENP8 Q96LD8 1/20 0.47
SENP7 Q9BQF6 1/20 0.47

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
SCHEMBL26813895 1.00 SMN1; SMN2 (0.54) SMN1; SMN2GAAHPGDNPSR1RAB9A
SCHEMBL26101354 1.00 SMN1; SMN2 (0.54) SMN1; SMN2GAAHPGDNPSR1RAB9A
SCHEMBL30274282 1.00 SMN1; SMN2 (0.54) SMN1; SMN2GAAHPGDNPSR1RAB9A
SCHEMBL30392446 1.00 SMN1; SMN2 (0.54) SMN1; SMN2GAAHPGDNPSR1RAB9A
SCHEMBL30392640 1.00 SMN1; SMN2 (0.54) SMN1; SMN2GAAHPGDNPSR1RAB9A
SCHEMBL3892107 1.00 SMN1; SMN2 (0.54) SMN1; SMN2GAAHPGDNPSR1RAB9A
SCHEMBL23720311 1.00 SMN1; SMN2 (0.54) SMN1; SMN2GAAHPGDNPSR1RAB9A
SCHEMBL19541802 1.00 SMN1; SMN2 (0.54) SMN1; SMN2GAAHPGDNPSR1RAB9A
SCHEMBL230525 1.00 SMN1; SMN2 (0.54) SMN1; SMN2GAAHPGDNPSR1RAB9A
SCHEMBL30274320 0.98 SMN1; SMN2 (0.55) SMN1; SMN2GAAHPGDNPSR1RAB9A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0406502-B1 Process for the preparation of (-)2-(2-(2-aminoethoxy)ethoxy)methyl)-4-(2, 3-dichlorophenyl)-3-ethoxycarbonyl-5-methoxycarbonyl-6-methyl-1,4-dihydropyridine, and intermediate for its preparation ADIR (FR) 1995-05-10 EP claimed
US-4983740-A Multistep; from 2- 2-/2-chloroethoxy/ethoxy!ethanol and potassium phthalimide ADIR ET COMPAGNIE (FR) 1991-01-08 US claimed
EP-3886904-B1 IRAK DEGRADERS AND USES THEREOF KYMERA THERAPEUTICS INC (US) 2026-04-22 EP disclosed
US-12528785-B2 MDM2 degraders and uses thereof KYMERA THERAPEUTICS, INC. (US) 2026-01-20 US disclosed
US-20250325673-A1 IRAK DEGRADERS AND USES THEREOF KYMERA THERAPEUTICS INC (US) 2025-10-23 US disclosed
EP-4613773-A2 IRAK DEGRADERS AND USES THEREOF Kymera Therapeutics, Inc. (US) 2025-09-10 EP disclosed
EP-3731869-B1 IRAK DEGRADERS AND USES THEREOF KYMERA THERAPEUTICS INC (US) 2025-07-23 EP disclosed
US-20250163042-A1 IRAK DEGRADERS AND USES THEREOF KYMERA THERAPEUTICS, INC. 2025-05-22 US disclosed
US-12258341-B2 IRAK degraders and uses thereof KYMERA THERAPEUTICS, INC. (US) 2025-03-25 US disclosed
US-20250000985-A1 IRAK DEGRADERS AND USES THEREOF KYMERA THERAPEUTICS, INC. 2025-01-02 US disclosed
US-20240424110-A1 MDM2 DEGRADERS AND USES THEREOF KYMERA THERAPEUTICS, INC. 2024-12-26 US disclosed
US-9932331-B2 Phenyl tetrahydroisoquinoline compound substituted with heteroaryl TAISHO PHARMACEUTICAL CO., LTD. (JP) 2018-04-03 US disclosed
US-20170210736-A1 PHENYL TETRAHYDROISOQUINOLINE COMPOUND SUBSTITUTED WITH HETEROARYL TAISHO PHARMACEUTICAL CO., LTD (JP) 2017-07-27 US disclosed
EP-3173408-A1 PHENYL TETRAHYDROISOQUINOLINE COMPOUND SUBSTITUTED WITH HETEROARYL Taisho Pharmaceutical Co., Ltd. (JP) 2017-05-31 EP disclosed
WO-2009060158-A1 4- (4-CYANOPHENYL) -1- (3-TRIFLUOROMETHYLPHENYL) -3,4, 6, 7-TETRAHYDRO-1H-PYRROLO [3, 4- D] PYRIMIDINE-2, 5-DIONE DERIVATIVES AND THEIR USE AS HUMAN NEUTROPHIL ELASTASE INHIBITORS ARGENTA DISCOVERY LIMITED (GB) 2009-05-14 WO disclosed
US-7164014-B2 Protected linker compounds LINDEN TECHNOLOGIES, INC. (US) 2007-01-16 US disclosed
US-20030105056-A1 Protected linker compounds LINDEN TECHNOLOGIES, INC. 2003-06-05 US disclosed
WO-2003027314-A2 PROTECTED LINKER COMPOUNDS LINDEN TECHNOLOGIES, INC. (US) 2003-04-03 WO disclosed
US-5026863-A Medicinal products in racemic or enantiomorph form; calcium channel blockers. hypotensive agents, cardiovascular disorders ADIR ET COMPAGNIE (FR) 1991-06-25 US disclosed
US-4983740-A Multistep; from 2- 2-/2-chloroethoxy/ethoxy!ethanol and potassium phthalimide ADIR ET COMPAGNIE (FR) 1991-01-08 US 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 (8 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-20250325673-A1 IRAK DEGRADERS AND USES THEREOF IRAK2, IRAK3, IRAK1 SMN1; SMN2 2647/4885GAA 1234/4885HPGD 3843/4885
US-12258341-B2 IRAK degraders and uses thereof IRAK2, IRAK3, IRAK1 SMN1; SMN2 2647/4885GAA 1234/4885HPGD 3843/4885
US-20250163042-A1 IRAK DEGRADERS AND USES THEREOF IRAK2, IRAK3, IRAK1 SMN1; SMN2 2647/4885GAA 1234/4885HPGD 3843/4885
US-20250000985-A1 IRAK DEGRADERS AND USES THEREOF IRAK2, IRAK3, IRAK1 SMN1; SMN2 2647/4885GAA 1234/4885HPGD 3843/4885
US-20240424110-A1 MDM2 DEGRADERS AND USES THEREOF MDM2, USP2, MYCBP2 SMN1; SMN2 2413/4885GAA 1436/4885HPGD 3207/4885
US-12528785-B2 MDM2 degraders and uses thereof MDM2, ADRM1, RBX1 SMN1; SMN2 737/4885GAA 2635/4885HPGD 4011/4885
US-20030105056-A1 Protected linker compounds NSUN2, MTAP, TYMP SMN1; SMN2 469/4885GAA 2765/4885HPGD 4100/4885
US-20170210736-A1 PHENYL TETRAHYDROISOQUINOLINE COMPOUND SUBSTITUTED WITH HETEROARYL NHERF1, SLC9A3, SLC26A3 SMN1; SMN2 4511/4885GAA 2816/4885HPGD 3339/4885

“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.