Testosterone Propionate

Testosterone Propionate

SCHEMBL8724796

CCC(=O)O[C@@H]1CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3CC[C@]12C

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

AR

The experimentally established mechanism targets of Testosterone Propionate. 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
AR known ✓ P10275 4/20 1.00
CYP3A4 P08684 8/20 1.00
LMNA P02545 8/20 1.00
TSHR P16473 5/20 1.00
MAPT P10636 5/20 1.00
NR3C1 P04150 4/20 1.00
PGR P06401 4/20 1.00
NR1I2 O75469 3/20 1.00
CYP2C9 P11712 3/20 1.00
CYP2C19 P33261 2/20 1.00
CYP17A1 P05093 1/20 1.00
OPRK1 P41145 1/20 1.00
CYP19A1 P11511 4/20 0.83
PSEN1 P49768 1/20 0.66
PSEN2 P49810 1/20 0.66
APH1B Q8WW43 1/20 0.66
NCSTN Q92542 1/20 0.66
APH1A Q96BI3 1/20 0.66
PSENEN Q9NZ42 1/20 0.66
HSD17B10 Q99714 4/20 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
Testosterone Propionate SCHEMBL30829229 1.00 CYP3A4 (1.00) CYP3A4LMNATSHRMAPTNR3C1
Testosterone Propionate SCHEMBL4044 1.00 CYP3A4 (1.00) CYP3A4LMNATSHRMAPTNR3C1
Testosterone Propionate SCHEMBL18438820 1.00 CYP3A4 (1.00) CYP3A4LMNATSHRMAPTNR3C1
Testosterone Propionate SCHEMBL5460173 1.00 CYP3A4 (1.00) CYP3A4LMNATSHRMAPTNR3C1
Testosterone Propionate SCHEMBL14360596 1.00 CYP3A4 (1.00) CYP3A4LMNATSHRMAPTNR3C1
Testosterone Propionate SCHEMBL25083388 1.00 CYP3A4 (1.00) CYP3A4LMNATSHRMAPTNR3C1
Testosterone Propionate SCHEMBL18438872 1.00 CYP3A4 (1.00) CYP3A4LMNATSHRMAPTNR3C1
Testosterone Propionate SCHEMBL21256102 1.00 CYP3A4 (1.00) CYP3A4LMNATSHRMAPTNR3C1
Testosterone Propionate SCHEMBL22417524 1.00 CYP3A4 (1.00) CYP3A4LMNATSHRMAPTNR3C1
Testosterone Propionate SCHEMBL28227392 0.99 CYP3A4 (0.98) CYP3A4LMNATSHRMAPTNR3C1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0335545-B2 Pharmaceutical formulations for parenteral use UNIV FLORIDA (US) 1998-09-23 EP disclosed
EP-0327766-B1 Redox systems for brain-targeted drug delivery UNIV FLORIDA (US) 1998-04-08 EP disclosed
US-5024998-A Administering in aqueous solution with cyclodextrin derivative UNIVERSITY OF FLORIDA (US) 1991-06-18 US disclosed
US-5017566-A Redox systems for brain-targeted drug delivery UNIVERSITY OF FLORIDA (US) 1991-05-21 US disclosed
US-5002935-A Inclusion Complexing Hydroxypropylcyclodextrin with a Dihydropyridine-substituted Drug UNIVERSITY OF FLORIDA (US) 1991-03-26 US disclosed
US-4983586-A Decreasing precipitation at injection site or in lungs or other organs by combining with hydroxypropyl-beta-cyclodextrin UNIVERSITY OF FLORIDA (US) 1991-01-08 US disclosed
EP-0335545-A2 Pharmaceutical formulations for parenteral use UNIVERSITY OF FLORIDA (US) 1989-10-04 EP disclosed
EP-0327766-A2 Redox systems for brain-targeted drug delivery UNIVERSITY OF FLORIDA (US) 1989-08-16 EP disclosed