SCHEMBL5479018

SCHEMBL5479018

Cc1ccc2oc(N3C(=O)CCC3=O)nc2c1

nearest known ligand 0.51

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ GABRP O00591 1/20 0.51
▸ GABRD O14764 1/20 0.51
▸ GABRA1 P14867 1/20 0.51
▸ GABRB1 P18505 1/20 0.51
▸ GABRG2 P18507 1/20 0.51
▸ GABRB3 P28472 1/20 0.51
▸ GABRA5 P31644 1/20 0.51
▸ GABRA3 P34903 1/20 0.51
▸ GABRA2 P47869 1/20 0.51
▸ GABRB2 P47870 1/20 0.51
▸ GABRA4 P48169 1/20 0.51
▸ GABRE P78334 1/20 0.51
▸ GABRA6 Q16445 1/20 0.51
▸ GABRG1 Q8N1C3 1/20 0.51
▸ GABRG3 Q99928 1/20 0.51
▸ GABRQ Q9UN88 1/20 0.51
▸ NPC1 O15118 7/20 0.47
▸ RAB9A P51151 7/20 0.47
▸ KDM4E B2RXH2 5/20 0.47
▸ ALDH1A1 P00352 5/20 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
SCHEMBL13765048 0.82 SMN1; SMN2 (0.46) GABRPGABRDGABRA1GABRB1GABRG2
SCHEMBL5476977 0.80 GABRP (0.39) GABRPGABRDGABRA1GABRB1GABRG2
SCHEMBL27938096 0.72 RAB9A (0.53) GABRPGABRDGABRA1GABRB1GABRG2
SCHEMBL28473715 0.72 FAAH (0.60) NPC1RAB9AKDM4EALDH1A1HPGD
SCHEMBL6499067 0.72 FAAH (0.49) NPC1RAB9AKDM4EALDH1A1HPGD
SCHEMBL6501249 0.71 HTR6 (0.53) GABRPGABRDGABRA1GABRB1GABRG2
SCHEMBL8346086 0.71 NPC1 (0.58) NPC1RAB9AKDM4EALDH1A1HPGD
SCHEMBL9105844 0.70 NPC1 (0.61) NPC1RAB9AKDM4EALDH1A1HPGD
SCHEMBL903255 0.70 NPC1 (0.61) NPC1RAB9AKDM4EALDH1A1HPGD
SCHEMBL29442076 0.70 NPC1 (0.61) NPC1RAB9AKDM4EALDH1A1HPGD

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 11 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20070207972-A1 Processes for the preparation of 0-(2-aminobenzo[d]oxazol-5-yl)methyl hydroxylamine for the synthesis of 6,11-bicyclic erythromycin derivative EDP-182 ENANTA PHARMACEUTICALS, INC. 2007-09-06 — — US claimed
US-20100041618-A1 6-11 Bridged Oxime Erythromycin Derivatives ENANTA PHARMACEUTICALS, INC. 2010-02-18 — — US disclosed
US-20100041618-A1 6-11 Bridged Oxime Erythromycin Derivatives ENANTA PHARMACEUTICALS, INC. 2010-02-18 — — US disclosed
US-7563877-B2 Processes for the preparation of 0-(2-aminobenzo[d]oxazol-5-yl)methyl hydroxylamine for the synthesis of 6,11-bicyclic erythromycin derivative EDP-182 ENANTA PHARMACEUTICALS, INC. (US) 2009-07-21 — — US disclosed
US-7563877-B2 Processes for the preparation of 0-(2-aminobenzo[d]oxazol-5-yl)methyl hydroxylamine for the synthesis of 6,11-bicyclic erythromycin derivative EDP-182 ENANTA PHARMACEUTICALS, INC. (US) 2009-07-21 — — US disclosed
US-20080262208-A1 6-11 Bridged Oxime Erythromycin Derivatives WANG GUOQIANG 2008-10-23 — — US disclosed
US-20080262208-A1 6-11 Bridged Oxime Erythromycin Derivatives WANG GUOQIANG 2008-10-23 — — US disclosed
US-7384922-B2 6-11 bridged oxime erythromycin derivatives ENANTA PHARMACEUTICALS, INC. (US) 2008-06-10 — — US disclosed
US-7384922-B2 6-11 bridged oxime erythromycin derivatives ENANTA PHARMACEUTICALS, INC. (US) 2008-06-10 — — US disclosed
US-20070207972-A1 Processes for the preparation of 0-(2-aminobenzo[d]oxazol-5-yl)methyl hydroxylamine for the synthesis of 6,11-bicyclic erythromycin derivative EDP-182 ENANTA PHARMACEUTICALS, INC. 2007-09-06 — — US disclosed
US-20070207972-A1 Processes for the preparation of 0-(2-aminobenzo[d]oxazol-5-yl)methyl hydroxylamine for the synthesis of 6,11-bicyclic erythromycin derivative EDP-182 ENANTA PHARMACEUTICALS, INC. 2007-09-06 — — 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 (3 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-20100041618-A1 6-11 Bridged Oxime Erythromycin Derivatives CYP2D6, CYP2B6, CYP1B1 GABRP 4297/4885GABRD 4242/4885GABRA1 3985/4885
US-20070207972-A1 Processes for the preparation of 0-(2-aminobenzo[d]oxazol-5-yl)methyl hydroxylamine for the synthesis of 6,11-bicyclic erythromycin derivative EDP-182 DHPS, TET1, TET2 GABRP 1621/4885GABRD 1902/4885GABRA1 2624/4885
US-20080262208-A1 6-11 Bridged Oxime Erythromycin Derivatives CYP2D6, CYP2B6, CYP1B1 GABRP 4297/4885GABRD 4242/4885GABRA1 3985/4885

“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.

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