SCHEMBL29637786

SCHEMBL29637786

Cc1cc(-c2ccc(N=Nc3c(N)ccc4cc(S(=O)(=O)O)ccc34)c(C)c2)ccc1N=Nc1c(N)ccc2cc(S(=O)(=O)O)ccc12.[Na+]

nearest known ligand 0.84

Known targets — ChEMBL curated mechanism

ABCC8ACEADORA1ADORA2AADORA2BADORA3ALDH5A1ALOX5ALOX5APATP4AATP4BBRAFCA1CA12CA2CA4CYSLTR1DHFRDPEP1EDNRAEDNRBESR2F10FDPSFGF1GABBR1GABBR2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGARTGNRHRGSC1HMGCRIMPDH1IMPDH2KCNJ11LY96NOD2NR3C1NS3NS4ANS5bP2RY1P2RY12P2RY2P2RY4P2RY6PBP2XPDE3APDE3BPDE4APDE4BPDE4CPDE4DPDK1PDK2PDK3PDK4PPARGPPATPTGIRPTGS1PTGS2RAF1RYR1RYR3SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASERPINC1SLC12A1SLC12A3SYKTHRATHRBTLR3TLR4TLR9TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYMSVKORC1XDHblablaIMP-1blaOXA-33blaOXA-58blaT-3blaT-4blaT-5blaT-6dacAdacBdacCfolAfolPfolP1ftsIfusAgaggyrAgyrBmecAmrcAmrcBmrdApbp1apbp1bpbp2pbp2apbp2bpbp3pbp4pbpApbpBpbpCpbpFpolponBrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpoArpoBrpoCrpoZrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

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
▸ THRB known ✓ P10828 3/20 0.51
▸ SUMO2 P61956 2/20 0.84
▸ SUMO1 P63165 2/20 0.84
▸ SENP7 Q9BQF6 2/20 0.84
▸ SENP2 Q9HC62 2/20 0.84
▸ SENP3 Q9H4L4 1/20 0.84
▸ SENP1 Q9P0U3 1/20 0.84
▸ ENPP2 Q13822 6/20 0.63
▸ MEN1 O00255 3/20 0.60
▸ KMT2A Q03164 3/20 0.60
▸ HTT P42858 1/20 0.60
▸ ALDH1A1 P00352 4/20 0.57
▸ HIF1A Q16665 2/20 0.57
▸ PHLPP2 Q6ZVD8 2/20 0.53
▸ PTPN1 P18031 2/20 0.53
▸ USP2 O75604 1/20 0.53
▸ ATM Q13315 1/20 0.53
▸ L3MBTL1 Q9Y468 1/20 0.53
▸ CYP2C9 P11712 5/20 0.51
▸ HSD17B10 Q99714 5/20 0.51

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
SCHEMBL14413371 0.99 SUMO2 (0.86) SUMO2SUMO1SENP7SENP2SENP3
SCHEMBL4952032 0.99 SUMO2 (0.86) SUMO2SUMO1SENP7SENP2SENP3
SCHEMBL14418340 0.97 SUMO2 (0.83) SUMO2SUMO1SENP7SENP2SENP3
SCHEMBL19132261 0.94 SENP2 (0.78) SUMO2SUMO1SENP7SENP2SENP3
SCHEMBL29374866 0.92 SUMO2 (1.00) SUMO2SUMO1SENP7SENP2SENP3
SCHEMBL14418523 0.92 SUMO2 (1.00) SUMO2SUMO1SENP7SENP2SENP3
SCHEMBL14613567 0.91 SUMO2 (0.74) SUMO2SUMO1SENP7SENP2SENP3
SCHEMBL14418372 0.90 SUMO2 (0.72) SUMO2SUMO1SENP7SENP2SENP3
SCHEMBL12534468 0.87 SUMO2 (0.69) SUMO2SUMO1SENP7SENP2SENP3
SCHEMBL14583209 0.85 SUMO2 (0.67) SUMO2SUMO1SENP7SENP2SENP3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119139281-A New use of emodin as endoribonuclease inhibitor 中国中医科学院中医基础理论研究所 2024-12-17 — — CN disclosed
CN-111094474-B Near-infrared-curable ink composition, near-infrared-curable film, method for producing near-infrared-curable film, and method for photo-molding 住友金属矿山株式会社 2022-06-07 — — CN disclosed
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