Diflorasone Diacetate

Diflorasone Diacetate

SCHEMBL7101720

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

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

NR3C1

The experimentally established mechanism targets of Diflorasone Diacetate. 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 1.00
HIF1A Q16665 9/20 1.00
PGR P06401 7/20 1.00
AR P10275 6/20 1.00
CYP3A4 P08684 5/20 1.00
ALDH1A1 P00352 3/20 1.00
SMN1; SMN2 Q16637 3/20 1.00
CYP1A2 P05177 1/20 1.00
ADORA3 P0DMS8 3/20 0.71
CHRM1 P11229 1/20 0.71
ADRA1A P35348 1/20 0.71
LMNA P02545 3/20 0.67
MEN1 O00255 1/20 0.67
KMT2A Q03164 1/20 0.67
NR1I2 O75469 2/20 0.65
NR3C2 P08235 1/20 0.65
MAPT P10636 2/20 0.64
ABCB11 O95342 1/20 0.64
RAB9A P51151 1/20 0.64
NPSR1 Q6W5P4 1/20 0.64

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
Diflorasone Diacetate SCHEMBL10599667 1.00 HIF1A (1.00) HIF1APGRNR3C1ARCYP3A4
Diflorasone Diacetate SCHEMBL14410916 1.00 HIF1A (1.00) HIF1APGRNR3C1ARCYP3A4
Diflorasone Diacetate SCHEMBL4556 1.00 HIF1A (1.00) HIF1APGRNR3C1ARCYP3A4
Diflorasone Diacetate SCHEMBL14339606 1.00 HIF1A (1.00) HIF1APGRNR3C1ARCYP3A4
Diflorasone Diacetate SCHEMBL11020196 1.00 HIF1A (1.00) HIF1APGRNR3C1ARCYP3A4
Diflorasone Diacetate SCHEMBL11020199 1.00 HIF1A (1.00) HIF1APGRNR3C1ARCYP3A4
SCHEMBL11430576 0.94 NR3C1 (0.88) HIF1APGRNR3C1ARCYP3A4
SCHEMBL11423833 0.93 NR3C1 (0.87) HIF1APGRNR3C1ARCYP3A4
SCHEMBL11600201 0.92 NR3C1 (0.85) HIF1APGRNR3C1ARCYP3A4
SCHEMBL3164036 0.92 NR3C1 (0.85) HIF1APGRNR3C1ARCYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4041055-A SULFENYLATION, MICHAEL ADDITION, REACTION WITH THIOPHILE, HYDROLYSIS THE UPJOHN COMPANY (US) 1977-08-09 US claimed
US-3980778-A Anti-inflammatory steroid THE UPJOHN COMPANY (US) 1976-09-14 US claimed
US-20030130248-A1 Topical anti-inflammatory compositions AVENTIS PHARMACEUTICALS HOLDINGS INC. 2003-07-10 US disclosed
EP-0402963-A2 17-Alpha ethynyl steroids THE UPJOHN COMPANY (US) 1990-12-19 EP disclosed
US-4614621-A Ethynylation of 16-methylene-17-keto steroids THE UPJOHN COMPANY (US) 1986-09-30 US disclosed
US-4567001-A 16-Methylene-17α-hydroxy-progesterones THE UPJOHN COMPANY (US) 1986-01-28 US disclosed
US-4526720-A Process to prepare stabilized monolithium acetylide THE UPJOHN COMPANY (US) 1985-07-02 US disclosed
EP-0104054-A2 16-methylene-steroids and their preparation THE UPJOHN COMPANY (US) 1984-03-28 EP disclosed
US-4427591-A TOPICAL ANTIINFLAMMATORY AGENTS THE UPJOHN COMPANY (US) 1984-01-24 US disclosed
US-4336200-A 17α-Acyloxy-5β-corticoids THE UPJOHN COMPANY (US) 1982-06-22 US disclosed
US-4318853-A ANTIINFLAMMATORY AGENTS THE UPJOHN COMPANY (US) 1982-03-09 US disclosed
US-4083974-A Topical steroidal anti-inflammatory preparations containing polyoxypropylene 15 stearyl ether THE UPJOHN COMPANY (US) 1978-04-11 US disclosed
US-4018918-A ANTIINFLAMMATORY, ANTIMICROBIAL AGENTS THE UPJOHN COMPANY (US) 1977-04-19 US disclosed
US-4018918-A ANTIINFLAMMATORY, ANTIMICROBIAL AGENTS THE UPJOHN COMPANY (US) 1977-04-19 US disclosed
US-3980778-A Anti-inflammatory steroid THE UPJOHN COMPANY (US) 1976-09-14 US disclosed