Hydrocortisone

Hydrocortisone

SCHEMBL8190636

C[C@@H]1CC2C3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(OP(=O)([O-])[O-])C(=O)CO.C[C@@H]1CC2C3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(OP(=O)([O-])[O-])C(=O)CO.C[C@@H]1CC2C3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(OP(=O)([O-])[O-])C(=O)CO.C[C@]12CCC(=O)C=C1CCC1C2[C@@H](O)C[C@@]2(C)C1CC[C@]2(O)C(=O)CO.O=P([O-])([O-])[O-].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+]

nearest known ligand 0.57

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

NR3C1

The experimentally established mechanism targets of Hydrocortisone. 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 11/20 0.57
▸ CYP3A4 P08684 7/20 0.57
▸ HIF1A Q16665 5/20 0.57
▸ HSD17B10 Q99714 4/20 0.57
▸ PGR P06401 4/20 0.57
▸ KMT2A Q03164 3/20 0.57
▸ NFKB1 P19838 3/20 0.57
▸ CYP2C19 P33261 2/20 0.57
▸ MAPT P10636 2/20 0.57
▸ NR3C2 P08235 2/20 0.57
▸ SHBG P04278 1/20 0.57
▸ SERPINA6 P08185 1/20 0.57
▸ SMN1; SMN2 Q16637 1/20 0.57
▸ MEN1 O00255 2/20 0.56
▸ USP2 O75604 1/20 0.56
▸ MMP1 P03956 6/20 0.55
▸ TSHR P16473 2/20 0.53
▸ AR P10275 2/20 0.53
▸ CYP2D6 P10635 1/20 0.53
▸ APEX1 P27695 1/20 0.53

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
Dexamethasone SCHEMBL322760 0.89 HIF1A (0.69) NR3C1CYP3A4HIF1AHSD17B10PGR
Triamcinolone SCHEMBL593313 0.86 HIF1A (0.68) NR3C1CYP3A4HIF1AHSD17B10PGR
Betamethasone SCHEMBL28086533 0.85 HIF1A (0.66) NR3C1CYP3A4HIF1AHSD17B10PGR
Hydrocortisone Phosphoric Acid SCHEMBL8190634 0.85 HIF1A (0.66) NR3C1CYP3A4HIF1AHSD17B10PGR
SCHEMBL1048586 0.84 NR3C1 (0.75) NR3C1CYP3A4HIF1AHSD17B10PGR
SCHEMBL472227 0.84 NR3C1 (0.75) NR3C1CYP3A4HIF1AHSD17B10PGR
SCHEMBL337332 0.84 NR3C1 (0.75) NR3C1CYP3A4HIF1AHSD17B10PGR
Betamethasone Valerate SCHEMBL3670653 0.82 NR3C1 (0.70) NR3C1CYP3A4HIF1APGRKMT2A
Dexamethasone SCHEMBL4586353 0.81 HIF1A (0.56) NR3C1CYP3A4HIF1AHSD17B10PGR
Prednisolone Phosphoric Acid SCHEMBL7998176 0.80 CYP3A4 (0.71) NR3C1CYP3A4HIF1AHSD17B10PGR

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
EP-1008365-A1 DEVICE FOR IONTOPHORESIS Kowa Co., Ltd. (JP) 2000-06-14 — — EP disclosed
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