SCHEMBL1781200

SCHEMBL1781200

CC(=O)/C=C/c1ccccc1F

nearest known ligand 0.63

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
MAPT P10636 4/20 0.63
LMNA P02545 1/20 0.63
NFE2L2 Q16236 3/20 0.58
KDM4E B2RXH2 1/20 0.58
MAOB P27338 2/20 0.57
RAB9A P51151 4/20 0.55
SMN1; SMN2 Q16637 2/20 0.55
NPC1 O15118 1/20 0.55
IAPP P10997 1/20 0.55
CYP1B1 Q16678 2/20 0.54
CYP1A2 P05177 1/20 0.54
CYP2D6 P10635 1/20 0.54
GLA P06280 1/20 0.53
TDP1 Q9NUW8 1/20 0.53
RECQL P46063 1/20 0.53
KMT2A Q03164 1/20 0.51
ATM Q13315 1/20 0.51
L3MBTL1 Q9Y468 2/20 0.50
CYP1A1 P04798 1/20 0.49

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
SCHEMBL1781201 1.00 MAPT (0.63) MAPTLMNANFE2L2KDM4EMAOB
SCHEMBL31464870 1.00 MAPT (0.63) MAPTLMNANFE2L2KDM4EMAOB
SCHEMBL29374751 1.00 MAPT (0.63) MAPTLMNANFE2L2KDM4EMAOB
SCHEMBL14441077 0.85 MAPT (0.76) MAPTLMNANFE2L2KDM4ERAB9A
SCHEMBL3581314 0.83 NFE2L2 (0.62) MAPTLMNANFE2L2MAOBRAB9A
SCHEMBL3581316 0.83 NFE2L2 (0.62) MAPTLMNANFE2L2MAOBRAB9A
SCHEMBL29365442 0.82 CA1 (0.62) MAPTNFE2L2MAOBRAB9ASMN1; SMN2
SCHEMBL79638 0.82 CA1 (0.62) MAPTNFE2L2MAOBRAB9ASMN1; SMN2
SCHEMBL27829211 0.82 NFE2L2 (0.60) MAPTLMNANFE2L2MAOBRAB9A
SCHEMBL79637 0.82 CA1 (0.62) MAPTNFE2L2MAOBRAB9ASMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-112266352-B Piperlongumine derivative and preparation method and application thereof 绍兴文理学院 2022-02-08 CN disclosed
CN-112266352-A Piperlongumine derivative and preparation method and application thereof 绍兴文理学院 2021-01-26 CN disclosed
US-9540299-B2 MTOR-independent activator of TFEB for autophagy enhancement and uses thereof HONG KONG BAPTIST UNIVERSITY (HK) 2017-01-10 US disclosed
US-9540299-B2 MTOR-independent activator of TFEB for autophagy enhancement and uses thereof HONG KONG BAPTIST UNIVERSITY (HK) 2017-01-10 US disclosed
US-20160221907-A1 MTOR-independent activator of TFEB for autophagy enhancement and uses thereof HONG KONG BAPTIST UNIVERSITY (CN) 2016-08-04 US disclosed
US-20160221907-A1 MTOR-independent activator of TFEB for autophagy enhancement and uses thereof HONG KONG BAPTIST UNIVERSITY (CN) 2016-08-04 US disclosed
US-8592430-B2 Quinazolin-oxime derivatives as Hsp90 inhibitors DAC SLR (IT) 2013-11-26 US disclosed
EP-2144889-B1 QUINAZOLIN-OXIME DERIVATIVES AS HSP90 INHIBITORS DAC SRL (IT) 2012-08-29 EP disclosed
EP-2144889-B1 QUINAZOLIN-OXIME DERIVATIVES AS HSP90 INHIBITORS DAC SRL (IT) 2012-08-29 EP disclosed
US-20110118258-A1 QUINAZOLIN-OXIME DERIVATIVES AS HSP90 INHIBITORS DAC SRL (IT) 2011-05-19 US disclosed
US-20110118258-A1 QUINAZOLIN-OXIME DERIVATIVES AS HSP90 INHIBITORS DAC SRL (IT) 2011-05-19 US disclosed
US-20110118258-A1 QUINAZOLIN-OXIME DERIVATIVES AS HSP90 INHIBITORS DAC SRL (IT) 2011-05-19 US disclosed
EP-2144889-A2 QUINAZOLIN-OXIME DERIVATIVES AS HSP90 INHIBITORS DAC S.r.l. (IT) 2010-01-20 EP disclosed
WO-2008142720-A2 QUINAZOLIN-OXIME DERIVATIVES AS HSP90 INHIBITORS DAC SRL (IT) 2008-11-27 WO disclosed
WO-2008142720-A2 QUINAZOLIN-OXIME DERIVATIVES AS HSP90 INHIBITORS DAC SRL (IT) 2008-11-27 WO disclosed
US-7291743-B2 Isoxazole derivatives and methods of treating nitric oxide mediated diseases GENEBLUE CORPORATION (US) 2007-11-06 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 (2 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-20110118258-A1 QUINAZOLIN-OXIME DERIVATIVES AS HSP90 INHIBITORS HSP90AB1, HSP90AA1, HSP90B1 MAPT 296/4885LMNA 4565/4885NFE2L2 550/4885
US-20160221907-A1 MTOR-independent activator of TFEB for autophagy enhancement and uses thereof TFEB, SQSTM1, ATG7 MAPT 388/4885LMNA 2770/4885NFE2L2 161/4885

“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.