SCHEMBL5963314

SCHEMBL5963314

Cc1cn(-c2ccccc2)[nH]c1=O

nearest known ligand 0.68

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HPGD P15428 3/20 0.68
HSD17B10 Q99714 2/20 0.68
NPSR1 Q6W5P4 2/20 0.68
POLB P06746 1/20 0.68
SMN1; SMN2 Q16637 1/20 0.47
GAA P10253 4/20 0.43
ALOX15 P16050 1/20 0.43
KDM4E B2RXH2 2/20 0.40
ALDH1A1 P00352 2/20 0.40
TSHR P16473 1/20 0.40
CYP1A2 P05177 1/20 0.40
BLM P54132 1/20 0.40
KAT2B Q92831 1/20 0.39
MAPK1 P28482 1/20 0.39
HTT P42858 1/20 0.39
LMNA P02545 1/20 0.38
MAPT P10636 1/20 0.38
AURKA O14965 1/20 0.38
DAPK3 O43293 1/20 0.38
PDGFRA P16234 1/20 0.38

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
SCHEMBL11775647 0.76 SMN1; SMN2 (0.47) HPGDHSD17B10NPSR1POLBSMN1; SMN2
SCHEMBL564993 0.74 SMN1; SMN2 (0.46) HPGDHSD17B10NPSR1POLBSMN1; SMN2
SCHEMBL14221817 0.74 MAPT (0.53) HPGDHSD17B10NPSR1POLBGAA
SCHEMBL11000015 0.73 KDM4E (0.45) HPGDHSD17B10NPSR1POLBSMN1; SMN2
SCHEMBL4289304 0.71 MAPT (0.56) HPGDHSD17B10NPSR1SMN1; SMN2GAA
SCHEMBL4544224 0.69 SMN1; SMN2 (0.64) SMN1; SMN2GAAKDM4ETSHRLMNA
SCHEMBL7834516 0.69 HPGD (0.54) HPGDHSD17B10SMN1; SMN2KDM4EALDH1A1
SCHEMBL11394904 0.69 ALDH1A1 (0.50) HPGDHSD17B10NPSR1POLBSMN1; SMN2
SCHEMBL3248315 0.68 DYRK1A (0.43) HPGDHSD17B10NPSR1SMN1; SMN2GAA
SCHEMBL3655311 0.64 TSHR (0.48) HSD17B10SMN1; SMN2GAAKDM4ETSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-107922371-B N-substituted hydroxamic acids with carbon-based leaving groups as efficient HNO donors and uses thereof 约翰斯霍普金斯大学 2022-04-19 CN disclosed
EP-3313831-B1 N-SUBSTITUTED HYDROXAMIC ACIDS WITH CARBON-BASED LEAVING GROUPS AS EFFICIENT HNO DONORS AND USES THEREOF UNIV JOHNS HOPKINS (US) 2021-03-10 EP disclosed
US-10583141-B2 N-substituted hydroxamic acids with carbon-based leaving groups as efficient HNO donors and uses thereof THE JOHNS HOPKINS UNIVERSITY (US) 2020-03-10 US disclosed
US-20180185367-A1 N-SUBSTITUTED HYDROXAMIC ACIDS WITH CARBON-BASED LEAVING GROUPS AS EFFICIENT HNO DONORS AND USES THEREOF NATIONAL SCIENCE FOUNDATION 2018-07-05 US disclosed
EP-3313831-A1 N-SUBSTITUTED HYDROXAMIC ACIDS WITH CARBON-BASED LEAVING GROUPS AS EFFICIENT HNO DONORS AND USES THEREOF The Johns Hopkins University (US) 2018-05-02 EP disclosed
CN-107922371-A Hydroxamic acid of the substitutions of the N with carbon-based leaving group as effective HNO donors and application thereof 约翰斯霍普金斯大学 2018-04-17 CN disclosed
WO-2016210392-A1 N-SUBSTITUTED HYDROXAMIC ACIDS WITH CARBON-BASED LEAVING GROUPS AS EFFICIENT HNO DONORS AND USES THEREOF THE JOHNS HOPKINS UNIVERSITY (US) 2016-12-29 WO disclosed
EP-1716236-A2 ANTISENSE OLIGONUCLEOTIDES FOR TREATING UNWANTED PIGMENTATION OF THE SKIN AND HAIR Beiersdorf Aktiengesellschaft (DE) 2006-11-02 EP disclosed
WO-2005078090-A2 ANTISENSE OLIGONUCLEOTIDES FOR TREATING UNWANTED PIGMENTATION OF THE SKIN AND HAIR BEIERSDORF AG (DE) 2005-08-25 WO disclosed
EP-0591105-B1 Bisazo, bisazomethine and azo-azomethine compounds CIBA SC HOLDING AG (CH) 2001-10-24 EP 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-20180185367-A1 N-SUBSTITUTED HYDROXAMIC ACIDS WITH CARBON-BASED LEAVING GROUPS AS EFFICIENT HNO DONORS AND USES THEREOF HAAO, HAO2, HNMT HPGD 9/4885HSD17B10 177/4885NPSR1 1230/4885
US-10583141-B2 N-substituted hydroxamic acids with carbon-based leaving groups as efficient HNO donors and uses thereof HAAO, HAO2, HNMT HPGD 9/4885HSD17B10 177/4885NPSR1 1230/4885

“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.