Betamethasone Acetate

Betamethasone Acetate

SCHEMBL3882689

CC(=O)OCC(=O)[C@@]1(O)[C@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)C(O)C[C@@]21C.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 0.71

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

NR3C1

The experimentally established mechanism targets of Betamethasone Acetate. 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 7/20 0.71
▸ HIF1A Q16665 7/20 0.71
▸ CYP3A4 P08684 7/20 0.71
▸ LMNA P02545 3/20 0.71
▸ CYP2C9 P11712 1/20 0.71
▸ CNR1 P21554 1/20 0.71
▸ TBXA2R P21731 1/20 0.71
▸ SMN1; SMN2 Q16637 1/20 0.71
▸ KMT2A Q03164 3/20 0.64
▸ HSD17B10 Q99714 5/20 0.63
▸ PGR P06401 3/20 0.63
▸ TSHR P16473 2/20 0.63
▸ NFKB1 P19838 2/20 0.63
▸ AR P10275 2/20 0.63
▸ MEN1 O00255 2/20 0.63
▸ CYP2D6 P10635 1/20 0.63
▸ APEX1 P27695 1/20 0.63
▸ PMP22 Q01453 1/20 0.63
▸ NPSR1 Q6W5P4 1/20 0.63
▸ IKBKB O14920 1/20 0.63

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 SCHEMBL13724083 0.94 NR3C1 (0.72) HIF1ACYP3A4NR3C1LMNACYP2C9
Dexamethasone SCHEMBL1408949 0.94 NR3C1 (0.72) HIF1ACYP3A4NR3C1LMNACYP2C9
Dexamethasone SCHEMBL4743981 0.89 HSD17B10 (0.65) HIF1ACYP3A4NR3C1LMNACYP2C9
Triamcinolone SCHEMBL3043158 0.89 HSD17B10 (0.71) HIF1ACYP3A4NR3C1LMNACYP2C9
Amcinonide SCHEMBL2864339 0.86 HIF1A (0.74) HIF1ACYP3A4NR3C1LMNACYP2C9
Betamethasone Acetate SCHEMBL3681474 0.86 HIF1A (0.94) HIF1ACYP3A4NR3C1LMNACYP2C9
Dexamethasone SCHEMBL3135309 0.85 NR3C1 (0.68) HIF1ACYP3A4NR3C1LMNACYP2C9
Betamethasone SCHEMBL3224067 0.85 NR3C1 (0.68) HIF1ACYP3A4NR3C1LMNACYP2C9
Betamethasone Acetate SCHEMBL10412637 0.84 NR3C1 (1.00) HIF1ACYP3A4NR3C1LMNACYP2C9
Betamethasone Acetate SCHEMBL3625942 0.84 NR3C1 (1.00) HIF1ACYP3A4NR3C1LMNACYP2C9

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 24 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2007360-A1 CONTROLLED RELEASE DELIVERY DEVICE COMPRISING AN ORGANOSOL COAT Odidi, Isa (CA) 2008-12-31 — — EP claimed
WO-2007112581-A1 CONTROLLED RELEASE DELIVERY DEVICE COMPRISING AN ORGANOSOL COAT ODIDI ISA (CA) 2007-10-11 — — WO claimed
US-10624858-B2 Controlled release composition using transition coating, and method of preparing same INTELLIPHARMACEUTICS CORP (CA) 2020-04-21 — — US disclosed
US-10314787-B2 Controlled release delivery device comprising an organosol coat INTELLIPHARMACEUTICS CORPORATION (CA) 2019-06-11 — — US disclosed
US-20190083399-A9 DRUG DELIVERY COMPOSITION INTELLIPHARMACEUTICS CORPORATION (CA) 2019-03-21 — — US disclosed
US-20190076363-A1 CONTROLLED RELEASE DELIVERY DEVICE COMPRISING AN ORGANOSOL COAT INTELLIPHARMACEUTICS CORPORATION (CA) 2019-03-14 — — US disclosed
US-10159649-B2 Controlled release delivery device comprising an organosol coat INTELLIPHARMACEUTICS CORPORATION (CA) 2018-12-25 — — US disclosed
US-20170112770-A1 CONTROLLED RELEASE DELIVERY DEVICE COMPRISING AN ORGANOSOL COAT INTELLIPHARMACEUTICS CORPORATION (CA) 2017-04-27 — — US disclosed
US-9561188-B2 Controlled release delivery device comprising an organosol coat INTELLIPHARMACEUTICS CORPORATION (CA) 2017-02-07 — — US disclosed
EP-2007360-B1 CONTROLLED RELEASE DELIVERY DEVICE COMPRISING AN ORGANOSOL COAT ODIDI ISA (CA) 2014-11-26 — — EP disclosed
US-20090304787-A1 DRUG DELIVERY COMPOSITION ODIDI ISA 2009-12-10 — — US disclosed
WO-2007112579-A1 DRUG DELIVERY COMPOSITION ODIDI ISA (CA) 2007-10-11 — — WO disclosed
EP-1831389-A1 METHOD FOR BIOTRANSFORMATION OF THE CLYCLOSPORIN COMPOUND ISA247 Isotechnika Inc. (CA) 2007-09-12 — — EP disclosed
US-20070196914-A1 Methods for preparing oil bodies comprising active ingredients SEMBIOSYS GENETICS INC. (CA) 2007-08-23 — — US disclosed
WO-2006066416-A1 METHOD FOR BIOTRANSFORMATION OF THE CLYCLOSPORIN COMPOUND ISA247 ISOTECHNIKA INC. (CA) 2006-06-29 — — WO disclosed
EP-1670434-A1 METHODS FOR PREPARING OIL BODIES COMPRISING ACTIVE INGREDIENTS SemBioSys Genetics Inc. (CA) 2006-06-21 — — EP disclosed
US-20060039976-A1 Controlled release composition using transition coating, and method of preparing same INTELLIPHARMACEUTICS CORP (CA) 2006-02-23 — — US disclosed
US-20060024361-A1 Disintegrant assisted controlled release technology INTELLIPHARMACEUTICS CORP (CA) 2006-02-02 — — US disclosed
WO-2005030169-A1 METHODS FOR PREPARING OIL BODIES COMPRISING ACTIVE INGREDIENTS SEMBIOSYS GENETICS INC. (CA) 2005-04-07 — — WO disclosed
US-6645528-B1 Rate of dissolution of drugs can be enhanced by making the drug into a porous matrix form ACUSPHERE, INC. 2003-11-11 — — US disclosed
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