SCHEMBL29601134

SCHEMBL29601134

C[C@H](Nc1nc2c(-c3cnn(C)c3)nc(-c3ccc(Cl)cc3)cn2n1)C(=O)[O-].[Na+]

nearest known ligand 0.38

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
SYK known ✓ P43405 1/20 0.36
CA12 known ✓ O43570 1/20 0.35
CA1 known ✓ P00915 1/20 0.35
CA2 known ✓ P00918 1/20 0.35
PIK3CG P48736 1/20 0.38
RET P07949 5/20 0.38
CHEK1 O14757 1/20 0.37
JAK2 O60674 2/20 0.36
JAK1 P23458 2/20 0.36
TYK2 P29597 2/20 0.36
JAK3 P52333 2/20 0.36
CLK1 P49759 3/20 0.36
AHR P35869 1/20 0.36
EIF2AK4 Q9P2K8 1/20 0.36
MAPK1 P28482 2/20 0.35
CA9 Q16790 1/20 0.35
CCNT1 O60563 1/20 0.35
CCNB2 O95067 1/20 0.35
CCNE2 O96020 1/20 0.35
CDK1 P06493 1/20 0.35

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
SCHEMBL24327975 0.92 CHEK1 (0.39) PIK3CGRETCHEK1JAK2JAK1
SCHEMBL24327974 0.91 JAK2 (0.41) PIK3CGRETCHEK1JAK2JAK1
SCHEMBL28724034 0.91 JAK2 (0.41) PIK3CGRETCHEK1JAK2JAK1
SCHEMBL24327888 0.89 PIK3CG (0.38) PIK3CGRETCHEK1JAK2JAK1
SCHEMBL29601470 0.87 JAK2 (0.40) PIK3CGRETJAK2JAK1TYK2
SCHEMBL24327357 0.86 JAK2 (0.39) PIK3CGRETJAK2JAK1TYK2
SCHEMBL29601453 0.84 JAK2 (0.44) PIK3CGRETJAK2JAK1TYK2
SCHEMBL24327333 0.84 JAK2 (0.44) PIK3CGRETJAK2JAK1TYK2
SCHEMBL24327328 0.84 JAK2 (0.44) PIK3CGRETJAK2JAK1TYK2
SCHEMBL24327772 0.84 JAK2 (0.38) PIK3CGRETCHEK1JAK2JAK1

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-114369097-A Heteroaromatic AhR inhibitors 山东轩竹医药科技有限公司 2022-04-19 CN disclosed