Amcinonide

Amcinonide

SCHEMBL2864339

CC(=O)OCC(=O)[C@@]12OC3(CCCC3)O[C@@H]1C[C@H]1[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@@]12C.C[C@]12C=CC(=O)C=C1CC[C@@H]1[C@@H]2C(=O)C[C@@]2(C)[C@H]1CC[C@]2(O)C(=O)CO

nearest known ligand 0.74

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

NR3C1

The experimentally established mechanism targets of Amcinonide. 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 0.74
▸ HIF1A Q16665 10/20 0.74
▸ LMNA P02545 8/20 0.74
▸ CYP3A4 P08684 6/20 0.74
▸ PGR P06401 5/20 0.74
▸ NPSR1 Q6W5P4 2/20 0.74
▸ CNR1 P21554 2/20 0.74
▸ KCNH2 Q12809 1/20 0.74
▸ USP2 O75604 1/20 0.74
▸ MAPT P10636 1/20 0.74
▸ KMT2A Q03164 3/20 0.59
▸ NR1I2 O75469 1/20 0.58
▸ ALDH1A1 P00352 3/20 0.57
▸ HSD17B10 Q99714 4/20 0.55
▸ MEN1 O00255 2/20 0.55
▸ SLC29A1 Q99808 1/20 0.55
▸ TDP1 Q9NUW8 1/20 0.55
▸ CYP2C9 P11712 1/20 0.52
▸ TBXA2R P21731 1/20 0.52
▸ SMN1; SMN2 Q16637 1/20 0.52

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
Betamethasone Acetate SCHEMBL3882689 0.86 HIF1A (0.71) HIF1ALMNACYP3A4NR3C1PGR
Amcinonide SCHEMBL12396698 0.86 HIF1A (1.00) HIF1ALMNACYP3A4NR3C1PGR
Amcinonide SCHEMBL1649481 0.86 HIF1A (1.00) HIF1ALMNACYP3A4NR3C1PGR
Amcinonide SCHEMBL21051752 0.86 HIF1A (1.00) HIF1ALMNACYP3A4NR3C1PGR
Amcinonide SCHEMBL5488922 0.86 HIF1A (1.00) HIF1ALMNACYP3A4NR3C1PGR
Amcinonide SCHEMBL13026154 0.86 HIF1A (1.00) HIF1ALMNACYP3A4NR3C1PGR
Amcinonide SCHEMBL4720 0.86 HIF1A (1.00) HIF1ALMNACYP3A4NR3C1PGR
Amcinonide SCHEMBL1832816 0.84 LMNA (0.77) HIF1ALMNACYP3A4NR3C1PGR
Amcinonide SCHEMBL16093940 0.84 CYP3A4 (0.85) HIF1ALMNACYP3A4NR3C1PGR
Triamcinolone SCHEMBL3043158 0.82 HSD17B10 (0.71) HIF1ALMNACYP3A4NR3C1PGR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2253339-B1 A process for producing stents and corresponding stent SORIN BIOMEDICA CARDIO SRL (IT) 2011-12-28 — — EP disclosed
US-8084076-B2 Process for producing stents and corresponding stents SORIN BIOMEDICA CARDIO S.R.L. (IT) 2011-12-27 — — US disclosed
EP-2253339-A1 A process for producing stents and corresponding stent Sorin Biomedica Cardio S.r.l. (IT) 2010-11-24 — — EP disclosed
EP-1449546-B1 A process for producing stents and corresponding stent SORIN BIOMEDICA CARDIO SRL (IT) 2010-10-27 — — EP disclosed
US-20080140186-A1 PROCESS FOR PRODUCING STENTS AND CORRESPONDING STENTS SORIN BIOMEDICA CARDIO S.R.L. (IT) 2008-06-12 — — US disclosed
US-20040167612-A1 Process for producing stents and corresponding stents SORIN BIOMEDICA CARDIO S.R.L. (IT) 2004-08-26 — — US disclosed
EP-1449546-A1 A process for producing stents and corresponding stent SORIN BIOMEDICA S.p.A. (IT) 2004-08-25 — — EP disclosed
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