SCHEMBL384424

SCHEMBL384424

O=c1[nH][c]nc2ccsc12

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PDPK1 O15530 1/20 0.50
PARP1 P09874 1/20 0.50
SMN1; SMN2 Q16637 4/20 0.41
RAB9A P51151 3/20 0.41
MAPT P10636 4/20 0.38
SPR P35270 3/20 0.36
CASP3 P42574 1/20 0.35
SENP8 Q96LD8 1/20 0.35
SENP7 Q9BQF6 1/20 0.35
SENP6 Q9GZR1 1/20 0.35
L3MBTL1 Q9Y468 1/20 0.35
ADORA2A P29274 2/20 0.35
ADORA1 P30542 2/20 0.35
HCRTR1 O43613 1/20 0.34
ALOX15 P16050 1/20 0.34
TSHR P16473 1/20 0.34
MAPK1 P28482 1/20 0.34
HSD17B10 Q99714 1/20 0.34
HTT P42858 2/20 0.34
RXFP1 Q9HBX9 2/20 0.34

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
SCHEMBL2840643 0.71
SCHEMBL383127 0.69 KMT2A (0.44) PDPK1PARP1MAPTSPRADORA2A
SCHEMBL15668178 0.69 PDPK1 (0.39) PDPK1PARP1ADORA2AADORA1MEN1
SCHEMBL209626 0.67 PDPK1 (1.00) PDPK1PARP1SMN1; SMN2RAB9AMAPT
SCHEMBL2447243 0.65 CXCR2 (0.36)
Hydrochloric Acid SCHEMBL30700362 0.65 PDPK1 (0.96) PDPK1PARP1SMN1; SMN2RAB9AMAPT
SCHEMBL15668177 0.65 PDPK1 (0.38) PDPK1PARP1ADORA2AADORA1MEN1
SCHEMBL20458007 0.64 SMN1; SMN2 (0.54) PDPK1PARP1SMN1; SMN2RAB9AMAPT
SCHEMBL5068159 0.64 SMN1; SMN2 (0.54) PDPK1PARP1SMN1; SMN2RAB9AMAPT
SCHEMBL17893461 0.64 SMN1; SMN2 (0.54) PDPK1PARP1SMN1; SMN2RAB9AMAPT

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 213 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240228499-A1 MASP-2 INHIBITORS AND METHODS OF USE OMEROS CORPORATION (US) 2024-07-11 US disclosed
US-12030853-B2 MASP-2 inhibitors and methods of use OMEROS CORPORATION (US) 2024-07-09 US disclosed
US-20240210408-A1 USE OF DIVALENT METALS FOR ENHANCEMENT OF FLUORESCENT SIGNALS SONY GROUP CORP (JP) 2024-06-27 US disclosed
US-20240207423-A1 PROGAMMABLE POLYMERIC DRUGS SONY GROUP CORP (JP) 2024-06-27 US disclosed
US-12018159-B2 Ultra bright dimeric or polymeric dyes and methods for preparation of the same Sony Group Corporation (JP) 2024-06-25 US disclosed
US-12006438-B2 Polymeric dyes with linker groups comprising deoxyribose Sony Group Corporation (JP) 2024-06-11 US disclosed
WO-2024118840-A1 FUSED PYRIMIDINES AS MASP-2 INHIBITORS OMEROS CORPORATION (US) 2024-06-06 WO disclosed
WO-2024110803-A1 POLYMERIC COMPOUNDS COMPRISING ANTINEOPLASTIC AGENTS Sony Group Corporation (JP) 2024-05-30 WO disclosed
US-11981820-B2 Ultra bright dimeric or polymeric dyes Sony Group Corporation (JP) 2024-05-14 US disclosed
US-20240132725-A1 SPACING LINKER GROUP DESIGN FOR BRIGHTNESS ENHANCEMENT IN DIMERIC OR POLYMERIC DYES Sony Group Corporation (JP) 2024-04-25 US disclosed
WO-2013064984-A1 BIARYL ETHER SULFONAMIDES AND THEIR USE AS THERAPEUTIC AGENTS XENON PHARMACEUTICALS INC. (CA) 2013-05-10 WO disclosed
WO-2013064983-A1 BENZENESULFONAMIDE COMPOUNDS AND THEIR USE AS THERAPEUTIC AGENTS XENON PHARMACEUTICALS INC. (CA) 2013-05-10 WO disclosed
US-8415370-B2 Spiro-oxindole compounds and their uses as therapeutic agents XENON PHARMACEUTICALS INC. (CA) 2013-04-09 US disclosed
US-20120295897-A1 SPIRO-OXINDOLE COMPOUNDS AND THEIR USES AS THERAPEUTIC AGENTS XENON PHARMACEUTICALS INC. (CA) 2012-11-22 US disclosed
US-8263606-B2 Spiro-oxindole compounds and their use as therapeutic agents XENON PHARMACEUTICALS INC. (CA) 2012-09-11 US disclosed
US-8101647-B2 Spiro-oxindole compounds and their use as therapeutic agents XENON PHARMACEUTICALS INC. (CA) 2012-01-24 US disclosed
US-20110144139-A1 HEPSIN INHIBITORS FRED HUTCHINSON CANCER RESEARCH CENTER 2011-06-16 US disclosed
US-20100137299-A1 SPIRO-OXINDOLE COMPOUNDS AND THEIR USE AS THERAPEUTIC AGENTS XENON PHARMACEUTICALS INC. (CA) 2010-06-03 US disclosed
WO-2009151920-A2 HEPSIN INHIBITORS FRED HUTCHINSON CANCER RESEARCH CENTER (US) 2009-12-17 WO disclosed
WO-2008147864-A2 METHODS OF USING PIPERAZINE COMPOUNDS IN TREATING SODIUM CHANNEL-MEDIATED DISEASES OR CONDITIONS XENON PHARMACEUTICALS INC. (CA) 2008-12-04 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 (8 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-20240228499-A1 MASP-2 INHIBITORS AND METHODS OF USE MASP2, SPINT2, SERPINB1 PDPK1 2336/4885PARP1 743/4885SMN1; SMN2 3397/4885
US-11981820-B2 Ultra bright dimeric or polymeric dyes IK, MRPS2, UFM1 PDPK1 4357/4885PARP1 1015/4885SMN1; SMN2 1068/4885
US-20110144139-A1 HEPSIN INHIBITORS HPN, TMPRSS2, SPINT2 PDPK1 2660/4885PARP1 2174/4885SMN1; SMN2 4667/4885
US-20240207423-A1 PROGAMMABLE POLYMERIC DRUGS OPRM1, CHRM1, TUBB3 PDPK1 3126/4885PARP1 2171/4885SMN1; SMN2 1818/4885
US-12006438-B2 Polymeric dyes with linker groups comprising deoxyribose H1-0, POLM, H1-2 PDPK1 3252/4885PARP1 170/4885SMN1; SMN2 1000/4885
US-20120295897-A1 SPIRO-OXINDOLE COMPOUNDS AND THEIR USES AS THERAPEUTIC AGENTS TRPV3, TRPC3, TRPV1 PDPK1 2108/4885PARP1 3975/4885SMN1; SMN2 272/4885
US-20100137299-A1 SPIRO-OXINDOLE COMPOUNDS AND THEIR USE AS THERAPEUTIC AGENTS TRPV3, TRPV1, TRPC3 PDPK1 2005/4885PARP1 3928/4885SMN1; SMN2 289/4885
US-12030853-B2 MASP-2 inhibitors and methods of use MASP2, METAP2, SPINT2 PDPK1 1911/4885PARP1 2076/4885SMN1; SMN2 1476/4885

“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.