SCHEMBL29637809

SCHEMBL29637809

Cc1cc(-c2ccc(N=Nc3c(S(=O)(=O)[O-])cc4cc(S(=O)(=O)[O-])cc(N)c4c3O)c(C)c2)ccc1N=Nc1cc(S(=O)(=O)[O-])c2ccccc2c1O.[Na+].[Na+].[Na+]

nearest known ligand 0.83

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 5/20 0.57
▸ PTPN1 P18031 2/20 0.83
▸ USP2 O75604 2/20 0.83
▸ ATM Q13315 1/20 0.83
▸ L3MBTL1 Q9Y468 1/20 0.83
▸ PHLPP2 Q6ZVD8 3/20 0.76
▸ MEN1 O00255 4/20 0.63
▸ KMT2A Q03164 4/20 0.63
▸ HTT P42858 1/20 0.63
▸ CYP3A4 P08684 4/20 0.57
▸ MAPK1 P28482 4/20 0.57
▸ RECQL P46063 4/20 0.57
▸ HSD17B10 Q99714 4/20 0.57
▸ ALDH1A1 P00352 3/20 0.57
▸ ALOX15 P16050 3/20 0.57
▸ HPGD P15428 3/20 0.57
▸ ALOX12 P18054 2/20 0.57
▸ TSHR P16473 2/20 0.57
▸ ENPP2 Q13822 5/20 0.52
▸ ALB P02768 1/20 0.52

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
Trypan Blue Free Acid SCHEMBL9724 0.91 PTPN1 (1.00) PTPN1USP2ATML3MBTL1PHLPP2
Trypan Blue Free Acid SCHEMBL29371631 0.91 PTPN1 (1.00) PTPN1USP2ATML3MBTL1PHLPP2
Trypan Blue Free Acid SCHEMBL29350476 0.91 PTPN1 (1.00) PTPN1USP2ATML3MBTL1PHLPP2
Trypan Blue Free Acid SCHEMBL31686853 0.91 PTPN1 (1.00) PTPN1USP2ATML3MBTL1PHLPP2
SCHEMBL29382082 0.82 THRB (0.74) PTPN1USP2ATML3MBTL1PHLPP2
SCHEMBL29637844 0.82 PTPN1 (0.81) PTPN1USP2ATML3MBTL1PHLPP2
SCHEMBL20496488 0.80 PTPN1 (0.79) PTPN1USP2ATML3MBTL1PHLPP2
SCHEMBL29601587 0.80 PTPN1 (0.79) PTPN1USP2ATML3MBTL1PHLPP2
SCHEMBL29402157 0.80 PTPN1 (0.79) PTPN1USP2ATML3MBTL1PHLPP2
SCHEMBL10619886 0.79 PTPN1 (0.66) PTPN1USP2ATML3MBTL1PHLPP2

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
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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