Methylprednisolone 21-Suleptanic Acid Ester

Methylprednisolone 21-Suleptanic Acid Ester

SCHEMBL6259094

C=C1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@H]3[C@@H](O)C[C@]2(C)[C@@]1(O)C(=O)CO.C[C@H]1C[C@@H]2[C@H]([C@@H](O)C[C@@]3(C)[C@H]2CC[C@]3(O)C(=O)COC(=O)CCCCCCC(=O)N(C)CCS(=O)(=O)[O-])[C@@]2(C)C=CC(=O)C=C12.[Na+]

nearest known ligand 0.55

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Known targets — ChEMBL curated mechanism

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

The experimentally established mechanism targets of Methylprednisolone 21-Suleptanic Acid Ester. 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
NR3C1 known ✓ P04150 6/20 0.55
PDE4D known ✓ Q08499 1/20 0.52
HIF1A Q16665 9/20 0.55
LMNA P02545 2/20 0.55
CYP3A4 P08684 5/20 0.52
PGR P06401 5/20 0.52
AR P10275 2/20 0.52
F2 P00734 1/20 0.52
HSD17B10 Q99714 3/20 0.52
ABCB11 O95342 2/20 0.52
ALDH1A1 P00352 1/20 0.52
ABCC4 O15439 1/20 0.52
NR1I2 O75469 1/20 0.52
TNF P01375 2/20 0.49
IL6 P05231 1/20 0.49
SERPINA6 P08185 1/20 0.49
NR3C2 P08235 1/20 0.49
GLUL P15104 1/20 0.49
ADAM17 P78536 1/20 0.49
GPBAR1 Q8TDU6 1/20 0.49

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
Methylprednisolone 21-Suleptanic Acid Ester SCHEMBL43507 0.89 NR3C1 (0.69) HIF1ANR3C1LMNACYP3A4PGR
Methylprednisolone 21-Suleptanic Acid Ester SCHEMBL13524225 0.84 NR3C1 (0.70) HIF1ANR3C1LMNACYP3A4PGR
SCHEMBL11327186 0.80 HIF1A (0.82) HIF1ANR3C1LMNACYP3A4PGR
SCHEMBL11208820 0.80 HIF1A (0.82) HIF1ANR3C1LMNACYP3A4PGR
SCHEMBL11329958 0.80 NR3C1 (0.82) HIF1ANR3C1LMNACYP3A4PGR
SCHEMBL11201742 0.80 NR3C1 (0.82) HIF1ANR3C1LMNACYP3A4PGR
SCHEMBL13653761 0.80 NR3C1 (0.74) HIF1ANR3C1LMNACYP3A4PGR
Methylprednisolone SCHEMBL4274907 0.77 NR3C1 (0.87) HIF1ANR3C1LMNACYP3A4PGR
Methylprednisolone Hemisuccinate SCHEMBL582372 0.76 HIF1A (0.79) HIF1ANR3C1LMNACYP3A4PGR
Methylprednisolone Hemisuccinate SCHEMBL18321784 0.76 NR3C1 (0.81) HIF1ANR3C1LMNACYP3A4PGR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2005065185-A2 TEMPERATURE-STABLE FORMULATIONS, AND METHODS OF DEVELOPMENT THEREOF COLLEGIUM PHARMACEUTICALS, INC. (US) 2005-07-21 WO claimed
US-20050153946-A1 Temperature-stable formulations, and methods of development thereof COLLEGIUM PHARMACEUTICALS, INC. (US) 2005-07-14 US claimed
WO-2005065185-A2 TEMPERATURE-STABLE FORMULATIONS, AND METHODS OF DEVELOPMENT THEREOF COLLEGIUM PHARMACEUTICALS, INC. (US) 2005-07-21 WO disclosed
US-20050153946-A1 Temperature-stable formulations, and methods of development thereof COLLEGIUM PHARMACEUTICALS, INC. (US) 2005-07-14 US disclosed