Halcinonide

Halcinonide

SCHEMBL2637394

CC1(C)O[C@@H]2C[C@H]3[C@@H]4CCC5=CC(=O)CC[C@]5(C)[C@@]4(F)[C@@H](O)C[C@]3(C)[C@]2(C(=O)CCl)O1.C[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(O)C(=O)CO

nearest known ligand 0.73

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

NR3C1

The experimentally established mechanism targets of Halcinonide. 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 0.73
▸ CYP3A4 P08684 9/20 0.73
▸ PGR P06401 5/20 0.73
▸ AR P10275 3/20 0.73
▸ USP2 O75604 1/20 0.73
▸ HIF1A Q16665 7/20 0.70
▸ LMNA P02545 4/20 0.70
▸ NR1I2 O75469 1/20 0.70
▸ HSD17B10 Q99714 4/20 0.66
▸ NFKB1 P19838 3/20 0.66
▸ TSHR P16473 2/20 0.66
▸ PMP22 Q01453 2/20 0.66
▸ NPSR1 Q6W5P4 2/20 0.66
▸ MEN1 O00255 1/20 0.66
▸ CYP2D6 P10635 1/20 0.66
▸ KMT2A Q03164 1/20 0.66
▸ APEX1 P27695 1/20 0.66
▸ IKBKB O14920 1/20 0.66
▸ CHUK O15111 1/20 0.66
▸ ADRB2 P07550 1/20 0.66

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
Halcinonide SCHEMBL28142872 0.97 CYP3A4 (0.76) CYP3A4NR3C1PGRARUSP2
Halcinonide SCHEMBL9810174 0.93 CYP3A4 (0.68) CYP3A4NR3C1PGRARUSP2
Triamcinolone Acetonide SCHEMBL28103100 0.90 CYP3A4 (0.87) CYP3A4NR3C1PGRARHIF1A
Halcinonide SCHEMBL677232 0.87 CYP3A4 (0.71) CYP3A4NR3C1PGRARUSP2
Halcinonide SCHEMBL24015431 0.85 NR3C1 (1.00) CYP3A4NR3C1PGRARUSP2
Halcinonide SCHEMBL7861670 0.85 NR3C1 (1.00) CYP3A4NR3C1PGRARUSP2
Halcinonide SCHEMBL5188866 0.85 NR3C1 (1.00) CYP3A4NR3C1PGRARUSP2
Halcinonide SCHEMBL5489567 0.85 NR3C1 (1.00) CYP3A4NR3C1PGRARUSP2
Halcinonide SCHEMBL13026159 0.85 NR3C1 (1.00) CYP3A4NR3C1PGRARUSP2
Halcinonide SCHEMBL10019829 0.85 NR3C1 (1.00) CYP3A4NR3C1PGRARUSP2

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
CN-107208054-A Induced hepatocytes and uses thereof 艾克塞利瑞提德生物技术公司 2017-09-26 — — CN disclosed
US-20120125325-A1 THE USE OF AMLEXANOX IN THE THERAPY OF NEUTROPHIL-DRIVEN DISEASES BIOCOPEA, LTD. (GB) 2012-05-24 — — US disclosed
EP-2437741-A1 THE USE OF AMLEXANOX IN THE THERAPY OF NEUTROPHIL-DRIVEN DISEASES Biocopea Limited (GB) 2012-04-11 — — EP disclosed
WO-2010139985-A1 THE USE OF AMLEXANOX IN THE THERAPY OF NEUTROPHIL-DRIVEN DISEASES BIOCOPEA LIMITED (GB) 2010-12-09 — — WO disclosed
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