Known targets — ChEMBL curated mechanism
The experimentally established mechanism targets of Paramethasone 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)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | NR3C1 known ✓ | P04150 | 6/20 | 0.56 |
| ▸ | ABCB11 | O95342 | 3/20 | 1.00 |
| ▸ | PGR | P06401 | 8/20 | 0.79 |
| ▸ | AR | P10275 | 5/20 | 0.79 |
| ▸ | CYP3A4 | P08684 | 7/20 | 0.62 |
| ▸ | F2 | P00734 | 1/20 | 0.62 |
| ▸ | LMNA | P02545 | 2/20 | 0.55 |
| ▸ | ADRA1A | P35348 | 2/20 | 0.55 |
| ▸ | HSD17B10 | Q99714 | 2/20 | 0.55 |
| ▸ | KDM4E | B2RXH2 | 1/20 | 0.55 |
| ▸ | CYP2C19 | P33261 | 1/20 | 0.55 |
| ▸ | HTR1A | P08908 | 1/20 | 0.55 |
| ▸ | ADRA2A | P08913 | 1/20 | 0.55 |
| ▸ | HIF1A | Q16665 | 7/20 | 0.53 |
| ▸ | SMN1; SMN2 | Q16637 | 2/20 | 0.53 |
| ▸ | CYP2C9 | P11712 | 1/20 | 0.53 |
| ▸ | CNR1 | P21554 | 1/20 | 0.53 |
| ▸ | TBXA2R | P21731 | 1/20 | 0.53 |
| ▸ | ADORA3 | P0DMS8 | 1/20 | 0.53 |
| ▸ | CHRM1 | P11229 | 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.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| Paramethasone Acetate SCHEMBL11279748 | 1.00 | ABCB11 (1.00) | ABCB11PGRARCYP3A4F2 | |
| Paramethasone Acetate SCHEMBL7126 | 1.00 | ABCB11 (1.00) | ABCB11PGRARCYP3A4F2 | |
| Paramethasone Acetate SCHEMBL13423597 | 1.00 | ABCB11 (1.00) | ABCB11PGRARCYP3A4F2 | |
| Paramethasone Acetate SCHEMBL11070642 | 1.00 | ABCB11 (1.00) | ABCB11PGRARCYP3A4F2 | |
| Paramethasone Acetate SCHEMBL13929947 | 1.00 | ABCB11 (1.00) | ABCB11PGRARCYP3A4F2 | |
| Paramethasone Acetate SCHEMBL11443533 | 1.00 | ABCB11 (1.00) | ABCB11PGRARCYP3A4F2 | |
| SCHEMBL13929918 | 0.91 | ABCB11 (0.83) | ABCB11PGRARCYP3A4F2 | |
| SCHEMBL11742957 | 0.90 | ABCB11 (0.81) | ABCB11PGRARCYP3A4F2 | |
| Paramethasone SCHEMBL5579847 | 0.89 | PGR (0.96) | ABCB11PGRARCYP3A4F2 | |
| Paramethasone SCHEMBL11126091 | 0.89 | PGR (1.00) | ABCB11PGRARCYP3A4NR3C1 |
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 16 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-20180235882-A1 | TOPICAL COMPOSITIONS COMPRISING CORTICOSTEROIDS | CADILA HEALTHCARE LIMITED (IN) | 2018-08-23 | — | — | US | claimed |
| US-5426198-A | Contacting steroid in solution with chromium ion, hydrogen radical source, reducing agent | THE UPJOHN COMPANY (US) | 1995-06-20 | — | — | US | claimed |
| EP-0374185-B1 | IMPROVED 9$g(a)-DEHALOGENATION PROCESS | THE UPJOHN COMPANY (US) | 1993-02-10 | — | — | EP | claimed |
| EP-0374185-A1 | IMPROVED 9-g(a)-DEHALOGENATION PROCESS. | UPJOHN CO (US) | 1990-06-27 | — | — | EP | claimed |
| WO-1989001482-A1 | IMPROVED 9alpha-DEHALOGENATION PROCESS | THE UPJOHN COMPANY (US) | 1989-02-23 | — | — | WO | claimed |
| US-20180235882-A1 | TOPICAL COMPOSITIONS COMPRISING CORTICOSTEROIDS | CADILA HEALTHCARE LIMITED (IN) | 2018-08-23 | — | — | US | disclosed |
| US-5426198-A | Contacting steroid in solution with chromium ion, hydrogen radical source, reducing agent | THE UPJOHN COMPANY (US) | 1995-06-20 | — | — | US | disclosed |
| EP-0374185-B1 | IMPROVED 9$g(a)-DEHALOGENATION PROCESS | THE UPJOHN COMPANY (US) | 1993-02-10 | — | — | EP | disclosed |
| EP-0374185-A1 | IMPROVED 9-g(a)-DEHALOGENATION PROCESS. | UPJOHN CO (US) | 1990-06-27 | — | — | EP | disclosed |
| WO-1989001482-A1 | IMPROVED 9alpha-DEHALOGENATION PROCESS | THE UPJOHN COMPANY (US) | 1989-02-23 | — | — | WO | disclosed |
| EP-0186948-B1 | PROCESS AND INTERMEDIATES FOR THE PREPARATION OF 17ALPHA-HYDROXYPROGESTERONES AND CORTICOIDS FROM AN ENOL STEROID | THE UPJOHN COMPANY (US) | 1989-01-25 | — | — | EP | disclosed |
| US-4613463-A | Process and intermediates for the preparation of 17 alphahydroxyprogesterones and corticoids from an enol steroid | THE UPJOHN COMPANY (US) | 1986-09-23 | — | — | US | disclosed |
| EP-0186948-A1 | Process and intermediates for the preparation of 17alpha-hydroxyprogesterones and corticoids from an enol steroid | THE UPJOHN COMPANY (US) | 1986-07-09 | — | — | EP | disclosed |
| US-4472393-A | ANTIINFLAMMATORY AGENTS | SCHERING CORPORATION (US) | 1984-09-18 | — | — | US | disclosed |
| US-4305936-A | SOLUBILIZERS CONSISTING OF FATTY ACID GLYCERIDES, COCAMIDOPROPYL BETAINE AND A GLYCOL | DERMIK LABORATORIES (US) | 1981-12-15 | — | — | US | disclosed |
| US-4017615-A | ESPECIALLY USEFUL FOR ANTIINFLAMMATORY TOPICAL CORTICOIDS | SYNTEX CORPORATION (PM) | 1977-04-12 | — | — | US | disclosed |