SCHEMBL3044061

SCHEMBL3044061

CS(=O)(=O)O.CS(=O)(=O)O.O=c1[nH]c2c(c3c1CCCC3)Cc1c(CN3CCC(N4CCCC4)CC3)cccc1-2

nearest known ligand 0.40

Known targets — ChEMBL curated mechanism

ABL1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB2AGTR1BCL2BCL2A1BCL2L1BCL2L10BCL2L2BCRBRAFCHRM1CHRNA10CHRNA9DRD1DRD2DRD3DRD4DRD5EGFRF2FLT1FLT4GCKGHSRGNRHRGRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BHTR1AHTR1BHTR1DHTR2AHTR2CHTR3AIDH2KDRKITMAOBMCL1MTTPPP4HBPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PIKFYVEROCK1ROCK2SLC18A2SLC6A2SLC6A3SLC6A4TACR1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8gyrAgyrBparCparEpol

The experimentally established mechanism targets of None. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CHRM1 known ✓ P11229 4/20 0.38
DRD2 known ✓ P14416 1/20 0.38
ADRA1D known ✓ P25100 1/20 0.38
HTR2C known ✓ P28335 1/20 0.38
ADRA1A known ✓ P35348 1/20 0.38
ADRA1B known ✓ P35368 1/20 0.38
KDR known ✓ P35968 2/20 0.36
KIT known ✓ P10721 1/20 0.36
FLT1 known ✓ P17948 1/20 0.36
VEGFA P15692 1/20 0.40
EGLN1 Q9GZT9 1/20 0.40
RECQL P46063 2/20 0.39
L3MBTL1 Q9Y468 2/20 0.39
ALDH1A1 P00352 1/20 0.39
TSHR P16473 1/20 0.39
CHRM2 P08172 1/20 0.38
CHRM4 P08173 1/20 0.38
CHRM5 P08912 1/20 0.38
CHRM3 P20309 1/20 0.38
PARP1 P09874 5/20 0.37

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
SCHEMBL3063874 0.99 VEGFA (0.41) VEGFAEGLN1RECQLL3MBTL1ALDH1A1
SCHEMBL2778554 0.94 L3MBTL1 (0.44) RECQLL3MBTL1ALDH1A1TSHRCHRM1
SCHEMBL3054582 0.93 L3MBTL1 (0.46) VEGFAEGLN1RECQLL3MBTL1ALDH1A1
Hydrochloric Acid SCHEMBL3054664 0.92 L3MBTL1 (0.45) VEGFAEGLN1RECQLL3MBTL1ALDH1A1
SCHEMBL3060576 0.91 KDR (0.39) ALDH1A1PARP1KDRKITFLT1
SCHEMBL3062082 0.90 PARP1 (0.42) L3MBTL1ALDH1A1DRD2PARP1ACHE
SCHEMBL3060549 0.90 KDR (0.37) PARP1KDRKITFLT1
SCHEMBL3054604 0.87 DHODH (0.37) L3MBTL1PARP1KDRKITFLT1
SCHEMBL3049186 0.87 DHODH (0.37) L3MBTL1PARP1KDRKITFLT1
SCHEMBL3049179 0.87 DHODH (0.37) L3MBTL1PARP1KDRKITFLT1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20100261706-A1 SUBSTITUTED TETRACYCLIC 1H-INDENO [1,2-B]PYRIDINE-2(5H)-ONE ANALOGS THEREOF AND USES THEREOF INOTEK PHARMACEUTICALS CORPORATION (US) 2010-10-14 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-20100261706-A1 SUBSTITUTED TETRACYCLIC 1H-INDENO [1,2-B]PYRIDINE-2(5H)-ONE ANALOGS THEREOF AND USES THEREOF TNNI3, TNNT2, ALDH1A2 CHRM1 814/4885DRD2 2481/4885ADRA1D 61/4885

“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.