SCHEMBL499301

SCHEMBL499301

O=C(O)c1cc2ccccc2c(CP(=O)(O)O)n1

nearest known ligand 0.49

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
ACP3 P15309 1/20 0.45
KDM4E B2RXH2 1/20 0.42
MEN1 O00255 1/20 0.42
ALDH1A1 P00352 1/20 0.42
CYP1A2 P05177 1/20 0.42
GLA P06280 1/20 0.42
HPGD P15428 1/20 0.42
CYP2C19 P33261 1/20 0.42
KMT2A Q03164 1/20 0.42
HSD17B10 Q99714 1/20 0.42
GPR35 Q9HC97 2/20 0.41
POLB P06746 1/20 0.41
ALOX15 P16050 1/20 0.40
IGFBP3 P17936 2/20 0.39
IGFBP5 P24593 1/20 0.39
PGK1 P00558 1/20 0.39
PGK2 P07205 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
SCHEMBL28992943 0.80 ALOX15 (0.46) KDM4EMEN1ALDH1A1CYP1A2GLA
SCHEMBL4239380 0.77 KDM4E (0.49) KDM4EMEN1ALDH1A1CYP1A2GLA
Hydrochloric Acid SCHEMBL9602865 0.76 ALOX15 (0.50) ACP3ALDH1A1HPGDHSD17B10ALOX15
SCHEMBL4241096 0.76 DHODH (0.44) KDM4EMEN1ALDH1A1CYP1A2GLA
SCHEMBL4243783 0.75 DHODH (0.45) KDM4EMEN1ALDH1A1CYP1A2GLA
SCHEMBL1202286 0.74 ALOX15 (0.41) KDM4EMEN1ALDH1A1CYP1A2GLA
SCHEMBL1202536 0.72 ALOX15 (0.40) KDM4EMEN1ALDH1A1CYP1A2GLA
SCHEMBL4768998 0.72 KDM4E (0.52) KDM4EMEN1ALDH1A1CYP1A2GLA
SCHEMBL9327979 0.72 IGFBP3 (0.52) KDM4EMEN1ALDH1A1CYP1A2GLA
SCHEMBL14769120 0.71 ACP3 (0.54) ACP3ALDH1A1PGK1PGK2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8106043-B2 Benzoxazines, benzothiazines, and related compounds having NOS inhibitory activity NEURAXON, INC. (CA) 2012-01-31 US disclosed
US-20110212947-A1 SUBSTITUTED INDOLE COMPOUNDS HAVING NOS INHIBITORY ACTIVITY NEURAXON INC. (CA) 2011-09-01 US disclosed
US-7989447-B2 1,5 and 3,6-substituted indole compounds having NOS inhibitory activity NEURAXON, INC. (CA) 2011-08-02 US disclosed
US-7951940-B2 neuronal nitric oxide synthase (nNOS) isoform inhibitors; 2-ethyl-1-(1H-indol-5-yl)-isothiourea; neurogenerative disorders, stroke, reperfusion injury, head trauma, migraine headache, neuropathic pain, drug abuse, hyperalgesia NEURAXON, INC. (CA) 2011-05-31 US disclosed
US-7919510-B2 treatment or prevention of chronic pain, acute pain, migraine, and neuropathic pain; selectively inhibits neuronal nitric oxide synthase (nNOS) over endothelial nitric oxide synthase (eNOS) and/or inducible nitric oxide synthase (iNOS) NEURAXON, INC (CA) 2011-04-05 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 (1 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-20110212947-A1 SUBSTITUTED INDOLE COMPOUNDS HAVING NOS INHIBITORY ACTIVITY NOS2, NOS1, NOS3 ACP3 1922/4885KDM4E 2379/4885MEN1 3810/4885

“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.