Medroxyprogesterone Acetate

Medroxyprogesterone Acetate

SCHEMBL6563018

CC(=O)O[C@@]1(C(C)=O)CC[C@H]2[C@@H]3CC(C)C4=CC(=O)CC[C@]4(C)[C@H]3CC[C@@]21C

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

PGR

The experimentally established mechanism targets of Medroxyprogesterone 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
PGR known ✓ P06401 4/20 1.00
NR3C1 P04150 5/20 1.00
LMNA P02545 4/20 1.00
CYP3A4 P08684 4/20 1.00
AR P10275 4/20 1.00
SMN1; SMN2 Q16637 4/20 1.00
NPSR1 Q6W5P4 3/20 1.00
ABCB11 O95342 2/20 1.00
ALDH1A1 P00352 2/20 1.00
CHRM2 P08172 2/20 1.00
CHRM1 P11229 2/20 1.00
USP2 O75604 2/20 1.00
SHBG P04278 2/20 1.00
ABCC4 O15439 1/20 1.00
ESR1 P03372 1/20 1.00
NR3C2 P08235 1/20 1.00
HRH2 P25021 1/20 1.00
AKR1C3 P42330 1/20 1.00
AKR1C2 P52895 1/20 1.00
AKR1C1 Q04828 1/20 1.00

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
Medroxyprogesterone Acetate SCHEMBL13941346 1.00 NR3C1 (1.00) NR3C1LMNACYP3A4PGRAR
Medroxyprogesterone Acetate SCHEMBL14148331 1.00 NR3C1 (1.00) NR3C1LMNACYP3A4PGRAR
Medroxyprogesterone Acetate SCHEMBL3892232 1.00 NR3C1 (1.00) NR3C1LMNACYP3A4PGRAR
Medroxyprogesterone Acetate SCHEMBL14262777 1.00 NR3C1 (1.00) NR3C1LMNACYP3A4PGRAR
Medroxyprogesterone Acetate SCHEMBL4217893 1.00 NR3C1 (1.00) NR3C1LMNACYP3A4PGRAR
Medroxyprogesterone Acetate SCHEMBL4276 1.00 NR3C1 (1.00) NR3C1LMNACYP3A4PGRAR
Medroxyprogesterone Acetate SCHEMBL6835475 1.00 NR3C1 (1.00) NR3C1LMNACYP3A4PGRAR
Medroxyprogesterone Acetate SCHEMBL10080145 1.00 NR3C1 (1.00) NR3C1LMNACYP3A4PGRAR
Medroxyprogesterone Acetate SCHEMBL22761990 1.00 NR3C1 (1.00) NR3C1LMNACYP3A4PGRAR
Medroxyprogesterone Acetate SCHEMBL4277 0.98 NR3C1 (0.96) NR3C1LMNACYP3A4PGRAR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1399463-A1 PROCESS TO PREPARE 11$g(b),17$g(a),21-TRIHYDROXY-6$g(a)-METHYLPREGNA-1,4-DIENE-3,20-DIONE 21-ACETATE PHARMACIA & UPJOHN COMPANY (US) 2004-03-24 EP disclosed
EP-1399464-A1 PROCESS TO PREPARE 11BETA, 17ALPHA, 21-TRIHYDROXY-6ALPHA-METHYLPREGNA-1,4-DIENE-3,20-DIONE 21-ACETATE PHARMACIA & UPJOHN COMPANY (US) 2004-03-24 EP disclosed
WO-2002102827-A1 PROCESS TO PREPARE 11β, 17α,21-TRIHYDROXY-6α-METHYLPREGNA-1,4-DIENE-3,20-DIONE 21-ACETATE PHARMACIA & UPJOHN COMPANY (US) 2002-12-27 WO disclosed
WO-2002102826-A1 PROCESS TO PREPARE 11β,17α,21-TRIHYDROXY-6α-METHYLPREGNA-1,4-DIENE-3,20-DIONE 21-ACETATE PHARMACIA & UPJOHN COMPANY (US) 2002-12-27 WO disclosed
EP-0477195-A1 SURAMIN TYPE COMPOUNDS AND ANGIOSTATIC STEROIDS TO INHIBIT ANGIOGENESIS THE UPJOHN COMPANY (US) 1992-04-01 EP disclosed