SCHEMBL11591558

SCHEMBL11591558

c1ccc2c(c1)OCCOCCOc1ccccc1OCCOc1ccccc1OCCO2

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
▸ LMNA P02545 5/20 1.00
▸ SMN1; SMN2 Q16637 3/20 1.00
▸ CRHBP P24387 2/20 1.00
▸ CRHR2 Q13324 2/20 1.00
▸ HTT P42858 2/20 1.00
▸ ITGB2 P05107 1/20 0.82
▸ ICAM1 P05362 1/20 0.82
▸ ITGAL P20701 1/20 0.82
▸ GAA P10253 2/20 0.65
▸ ABCG2 Q9UNQ0 1/20 0.55
▸ KDM4E B2RXH2 3/20 0.55
▸ MAPT P10636 5/20 0.54
▸ BLM P54132 1/20 0.54
▸ NPSR1 Q6W5P4 1/20 0.50
▸ KMT2A Q03164 1/20 0.42
▸ MAOA P21397 1/20 0.39
▸ MAOB P27338 1/20 0.39

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
SCHEMBL676131 1.00 LMNA (1.00) LMNASMN1; SMN2CRHBPCRHR2HTT
SCHEMBL11505395 1.00 LMNA (1.00) LMNASMN1; SMN2CRHBPCRHR2HTT
SCHEMBL4920437 1.00 LMNA (1.00) LMNASMN1; SMN2CRHBPCRHR2HTT
SCHEMBL35765 1.00 LMNA (1.00) LMNASMN1; SMN2CRHBPCRHR2HTT
SCHEMBL10025196 1.00 LMNA (1.00) LMNASMN1; SMN2CRHBPCRHR2HTT
SCHEMBL687476 1.00 LMNA (1.00) LMNASMN1; SMN2CRHBPCRHR2HTT
SCHEMBL23658043 1.00 LMNA (1.00) LMNASMN1; SMN2CRHBPCRHR2HTT
SCHEMBL16076325 1.00 LMNA (1.00) LMNASMN1; SMN2CRHBPCRHR2HTT
SCHEMBL76331 1.00 LMNA (1.00) LMNASMN1; SMN2CRHBPCRHR2HTT
SCHEMBL10425464 1.00 LMNA (1.00) LMNASMN1; SMN2CRHBPCRHR2HTT

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-7230123-B2 Ureido or carbamate derivatives of crown ethers and of silicon usable for preparing supports intended for the separation by chromatography of metal cations and of organic molecules comprising amine functional groups COMMISSARIAT A L'ENERGIR ATOMIQUE (FR) 2007-06-12 — — US disclosed
US-7230123-B2 Ureido or carbamate derivatives of crown ethers and of silicon usable for preparing supports intended for the separation by chromatography of metal cations and of organic molecules comprising amine functional groups COMMISSARIAT A L'ENERGIR ATOMIQUE (FR) 2007-06-12 — — US disclosed
US-7211373-B2 Photothermographic material FUJIFILM CORPORATION (JP) 2007-05-01 — — US disclosed
US-7211373-B2 Photothermographic material FUJIFILM CORPORATION (JP) 2007-05-01 — — US disclosed
US-4110363-A FROM AN ALDEHYDE, ACID HALIDE AND CYANIDE, MACROCYCLIC POLYETHER CATALYST SHELL OIL COMPANY (US) 1978-08-29 — — US disclosed
US-4110360-A FROM AN ALDEHYDE, ACID HALIDE AND CYANIDE SHELL OIL COMPANY (US) 1978-08-29 — — US disclosed
Send feedback