Hydrocortisone

Hydrocortisone

SCHEMBL5699764

C[C@]12CCC(=O)C=C1CC[C@@H]1C2[C@@H](O)C[C@@]2(C)[C@H]1CC[C@]2(O)C(=O)CO

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

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 3/20 1.00
HIF1A Q16665 11/20 1.00
HSD17B10 Q99714 5/20 1.00
SERPINA6 P08185 4/20 1.00
CYP3A4 P08684 4/20 1.00
SMN1; SMN2 Q16637 4/20 1.00
NR3C2 P08235 4/20 1.00
CYP2C19 P33261 3/20 1.00
PGR P06401 3/20 1.00
KMT2A Q03164 2/20 1.00
SHBG P04278 2/20 1.00
NFKB1 P19838 2/20 1.00
MAPT P10636 2/20 1.00
LMNA P02545 3/20 0.80
AR P10275 2/20 0.78
CHRM1 P11229 1/20 0.78
PMP22 Q01453 2/20 0.73
TSHR P16473 2/20 0.73
BLM P54132 1/20 0.73
POLB P06746 1/20 0.69

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
Hydrocortisone SCHEMBL10292969 1.00 HIF1A (1.00) HIF1AHSD17B10SERPINA6CYP3A4SMN1; SMN2
Hydrocortisone SCHEMBL1560948 1.00 HIF1A (1.00) HIF1AHSD17B10SERPINA6CYP3A4SMN1; SMN2
Hydrocortisone SCHEMBL143923 1.00 HIF1A (1.00) HIF1AHSD17B10SERPINA6CYP3A4SMN1; SMN2
Hydrocortisone SCHEMBL6932400 1.00 HIF1A (1.00) HIF1AHSD17B10SERPINA6CYP3A4SMN1; SMN2
Hydrocortisone SCHEMBL1688689 1.00 HIF1A (1.00) HIF1AHSD17B10SERPINA6CYP3A4SMN1; SMN2
Hydrocortisone SCHEMBL24900238 1.00 HIF1A (1.00) HIF1AHSD17B10SERPINA6CYP3A4SMN1; SMN2
Hydrocortisone SCHEMBL19465688 1.00 HIF1A (1.00) HIF1AHSD17B10SERPINA6CYP3A4SMN1; SMN2
Hydrocortisone SCHEMBL10261067 1.00 HIF1A (1.00) HIF1AHSD17B10SERPINA6CYP3A4SMN1; SMN2
Hydrocortisone SCHEMBL12737556 1.00 HIF1A (1.00) HIF1AHSD17B10SERPINA6CYP3A4SMN1; SMN2
Hydrocortisone SCHEMBL13202859 1.00 HIF1A (1.00) HIF1AHSD17B10SERPINA6CYP3A4SMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1504021-B1 PROCESS FOR DEHYDROGENATION OF AZAANDROSTANE COMPOUNDS RICHTER GEDEON VEGYESZET (HU) 2006-07-12 EP claimed
EP-1504021-A1 PROCESS FOR DEHYDROGENATION OF AZAANDROSTANE COMPOUNDS RICHTER GEDEON VEGYESZETI GYAR R.T. (HU) 2005-02-09 EP claimed
US-6762302-B2 DEPROTONATION OF AZASTEROIDS USING CULTURES OF BIOCATALYSTS, OXIDOREDUCTASE ENZYMES, STABILIZERS, COMPLEXING AGENTS AND CHARGE TRANSFER COMPOUNDS, THEN INCUBATING GEDEON RICHTER, LTD. (HU) 2004-07-13 US claimed
WO-2003095472-A1 PROCESS FOR DEHYDROGENATION OF AZAANDROSTANE COMPOUNDS Richter Gedeon Vegyészeti Gyár Rt. (HU) 2003-11-20 WO claimed
US-20030215902-A1 Process for dehydrogenation of azaandros tane compounds RICHTER GEDEON VEGYESZETI GYAR RT. 2003-11-20 US claimed
US-20200339983-A1 BIOACTIVE CONJUGATES FOR OLIGONUCLEOTIDE DELIVERY UNIVERSITY OF MASSACHUSETTS 2020-10-29 US disclosed
US-8524697-B2 C20-C21 substituted glucocorticoid receptor agonists MERCK SHARP & DOHME CORP. (US) 2013-09-03 US disclosed
US-8524697-B2 C20-C21 substituted glucocorticoid receptor agonists MERCK SHARP & DOHME CORP. (US) 2013-09-03 US disclosed
US-20110262368-A1 C21 THIOETHERS AS GLUCOCORTICOID RECEPTOR AGONISTS SCHERING CORPORATION (US) 2011-10-27 US disclosed
US-20110262368-A1 C21 THIOETHERS AS GLUCOCORTICOID RECEPTOR AGONISTS SCHERING CORPORATION (US) 2011-10-27 US disclosed
US-20110182828-A1 C20-C21 SUBSTITUTED GLUCOCORTICOID RECEPTOR AGONISTS SCHERING CORPORATION (US) 2011-07-28 US disclosed
US-20110182828-A1 C20-C21 SUBSTITUTED GLUCOCORTICOID RECEPTOR AGONISTS SCHERING CORPORATION (US) 2011-07-28 US disclosed
EP-1504021-B1 PROCESS FOR DEHYDROGENATION OF AZAANDROSTANE COMPOUNDS RICHTER GEDEON VEGYESZET (HU) 2006-07-12 EP disclosed
EP-1504021-A1 PROCESS FOR DEHYDROGENATION OF AZAANDROSTANE COMPOUNDS RICHTER GEDEON VEGYESZETI GYAR R.T. (HU) 2005-02-09 EP disclosed
US-6762302-B2 DEPROTONATION OF AZASTEROIDS USING CULTURES OF BIOCATALYSTS, OXIDOREDUCTASE ENZYMES, STABILIZERS, COMPLEXING AGENTS AND CHARGE TRANSFER COMPOUNDS, THEN INCUBATING GEDEON RICHTER, LTD. (HU) 2004-07-13 US disclosed
WO-2003095472-A1 PROCESS FOR DEHYDROGENATION OF AZAANDROSTANE COMPOUNDS Richter Gedeon Vegyészeti Gyár Rt. (HU) 2003-11-20 WO disclosed
US-20030215902-A1 Process for dehydrogenation of azaandros tane compounds RICHTER GEDEON VEGYESZETI GYAR RT. 2003-11-20 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (3 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20110262368-A1 C21 THIOETHERS AS GLUCOCORTICOID RECEPTOR AGONISTS NR3C1, CYP4A11, NR3C2 NR3C1 1/4885HIF1A 3131/4885HSD17B10 765/4885
US-20200339983-A1 BIOACTIVE CONJUGATES FOR OLIGONUCLEOTIDE DELIVERY DCLRE1B, RTCB, RNASE1 NR3C1 2841/4885HIF1A 2687/4885HSD17B10 3222/4885
US-20110182828-A1 C20-C21 SUBSTITUTED GLUCOCORTICOID RECEPTOR AGONISTS NR3C1, MC2R, NR3C2 NR3C1 1/4885HIF1A 3951/4885HSD17B10 799/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.