SCHEMBL2362237

SCHEMBL2362237

O=C1Nc2ccccc2SC1c1ccncc1

nearest known ligand 0.49

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HSD17B10 Q99714 5/20 0.49
KDM4E B2RXH2 4/20 0.49
TDP1 Q9NUW8 2/20 0.49
USP2 O75604 1/20 0.49
ESR1 P03372 1/20 0.49
POLB P06746 1/20 0.49
THRB P10828 1/20 0.49
HPGD P15428 1/20 0.49
ALOX15 P16050 1/20 0.49
PTPN7 P35236 1/20 0.49
RECQL P46063 1/20 0.49
ESR2 Q92731 1/20 0.49
CTDSP1 Q9GZU7 1/20 0.49
CA2 P00918 1/20 0.47
GLA P06280 1/20 0.46
HTT P42858 2/20 0.45
MAPT P10636 6/20 0.44
GAA P10253 1/20 0.44
SMN1; SMN2 Q16637 3/20 0.44
ALDH1A1 P00352 3/20 0.44

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
SCHEMBL3626456 0.87 CA2 (0.62) HSD17B10KDM4ETDP1USP2ESR1
Hydrochloric Acid SCHEMBL10770897 0.85 CA2 (0.61) HSD17B10KDM4ETDP1USP2ESR1
SCHEMBL10650323 0.81 HSD17B10 (0.49) HSD17B10KDM4ETDP1USP2ESR1
SCHEMBL7278586 0.81 MAPT (0.62) HSD17B10KDM4ETDP1USP2ESR1
SCHEMBL7281597 0.81 HSD17B10 (0.52) HSD17B10KDM4ETDP1USP2ESR1
SCHEMBL17634130 0.81 MAPT (0.66) HSD17B10KDM4ETDP1USP2ESR1
SCHEMBL7278853 0.75 HSD17B10 (0.46) HSD17B10KDM4ETDP1USP2ESR1
SCHEMBL17634211 0.73 MAPT (0.46) HSD17B10KDM4ETDP1USP2ESR1
SCHEMBL10653449 0.72 HSD17B10 (0.49) HSD17B10KDM4ETDP1USP2ESR1
SCHEMBL10649115 0.72 MAPT (0.46) HSD17B10KDM4ETDP1USP2ESR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9193728-B2 Fused tetracyclic pyrido [4,3-B] indole and pyrido [3,4-B] indole derivatives and methods of use MEDIVATION TECHNOLOGIES, INC. (US) 2015-11-24 US disclosed
US-9193728-B2 Fused tetracyclic pyrido [4,3-B] indole and pyrido [3,4-B] indole derivatives and methods of use MEDIVATION TECHNOLOGIES, INC. (US) 2015-11-24 US disclosed
US-9193728-B2 Fused tetracyclic pyrido [4,3-B] indole and pyrido [3,4-B] indole derivatives and methods of use MEDIVATION TECHNOLOGIES, INC. (US) 2015-11-24 US disclosed
US-20130210803-A1 FUSED TETRACYCLIC PYRIDO [4,3-B] INDOLE AND PYRIDO [3,4-B] INDOLE DERIVATIVES AND METHODS OF USE MEDIVATION TECHNOLOGIES, INC. 2013-08-15 US disclosed
US-20130210803-A1 FUSED TETRACYCLIC PYRIDO [4,3-B] INDOLE AND PYRIDO [3,4-B] INDOLE DERIVATIVES AND METHODS OF USE MEDIVATION TECHNOLOGIES, INC. 2013-08-15 US disclosed
US-20130210803-A1 FUSED TETRACYCLIC PYRIDO [4,3-B] INDOLE AND PYRIDO [3,4-B] INDOLE DERIVATIVES AND METHODS OF USE MEDIVATION TECHNOLOGIES, INC. 2013-08-15 US disclosed
WO-2011103460-A1 FUSED TETRACYCLIC PYRIDO[4,3-B]INDOLE AND PYRIDO[3,4-B]ONDOLE DERIVATIVES AND METHODS OF USE MEDIVATION TECHNOLOGIES, INC. (US) 2011-08-25 WO 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-20130210803-A1 FUSED TETRACYCLIC PYRIDO [4,3-B] INDOLE AND PYRIDO [3,4-B] INDOLE DERIVATIVES AND METHODS OF USE HTR4, HTR3B, HTR2C HSD17B10 2249/4885KDM4E 1395/4885TDP1 856/4885

“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.