Budesonide

Budesonide

SCHEMBL10020756

CCCC1O[C@@H]2C[C@H]3[C@@H]4CCC5=CC(=O)C=C[C@]5(C)[C@H]4[C@@H](O)C[C@]3(C)C2(C(=O)CO)O1

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 Budesonide. 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 13/20 1.00
PGR P06401 7/20 1.00
CYP3A4 P08684 3/20 1.00
HIF1A Q16665 2/20 1.00
CYP2C9 P11712 2/20 1.00
ABCC3 O15438 1/20 1.00
ABCC4 O15439 1/20 1.00
ABCB11 O95342 1/20 1.00
IL5 P05113 1/20 1.00
NR3C2 P08235 1/20 1.00
AR P10275 1/20 1.00
CHRM1 P11229 1/20 1.00
MMP9 P14780 1/20 1.00
NFKB1 P19838 1/20 1.00
THPO P40225 1/20 1.00
SMN1; SMN2 Q16637 1/20 1.00
HSD17B10 Q99714 1/20 1.00
LMNA P02545 1/20 1.00
BLM P54132 1/20 1.00
PMP22 Q01453 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
Budesonide SCHEMBL16139563 1.00 NR3C1 (1.00) NR3C1PGRCYP3A4HIF1ACYP2C9
Budesonide SCHEMBL17168987 1.00 NR3C1 (1.00) NR3C1PGRCYP3A4HIF1ACYP2C9
Budesonide SCHEMBL9763339 1.00 NR3C1 (1.00) NR3C1PGRCYP3A4HIF1ACYP2C9
Budesonide SCHEMBL12440030 1.00 NR3C1 (1.00) NR3C1PGRCYP3A4HIF1ACYP2C9
Budesonide SCHEMBL19635 1.00 NR3C1 (1.00) NR3C1PGRCYP3A4HIF1ACYP2C9
Budesonide SCHEMBL17151422 1.00 NR3C1 (1.00) NR3C1PGRCYP3A4HIF1ACYP2C9
Budesonide SCHEMBL17971368 1.00 NR3C1 (1.00) NR3C1PGRCYP3A4HIF1ACYP2C9
Budesonide SCHEMBL13918824 1.00 NR3C1 (1.00) NR3C1PGRCYP3A4HIF1ACYP2C9
Budesonide SCHEMBL21570019 1.00 NR3C1 (1.00) NR3C1PGRCYP3A4HIF1ACYP2C9
Budesonide SCHEMBL10051995 1.00 NR3C1 (1.00) NR3C1PGRCYP3A4HIF1ACYP2C9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20170266137-A1 LIPOLYTIC METHODS NEOTHETICS, INC. 2017-09-21 US disclosed
US-20170266137-A1 LIPOLYTIC METHODS NEOTHETICS, INC. 2017-09-21 US disclosed
US-9707192-B2 Lipolytic methods NEOTHETICS, INC. (US) 2017-07-18 US disclosed
US-9707192-B2 Lipolytic methods NEOTHETICS, INC. (US) 2017-07-18 US disclosed
US-20160287611-A1 METHODS, COMPOSITIONS, AND FORMULATIONS FOR THE TREATMENT OF THYROID EYE DISEASE NEOTHETICS, INC. 2016-10-06 US disclosed
US-20160287611-A1 METHODS, COMPOSITIONS, AND FORMULATIONS FOR THE TREATMENT OF THYROID EYE DISEASE NEOTHETICS, INC. 2016-10-06 US disclosed
US-9452147-B2 Lipolytic methods NEOTHETICS, INC. (US) 2016-09-27 US disclosed
US-9452147-B2 Lipolytic methods NEOTHETICS, INC. (US) 2016-09-27 US disclosed
US-9370498-B2 Methods of using lipolytic formulations for regional adipose tissue treatment NEOTHETICS, INC. (US) 2016-06-21 US disclosed
US-9370498-B2 Methods of using lipolytic formulations for regional adipose tissue treatment NEOTHETICS, INC. (US) 2016-06-21 US disclosed
US-8420625-B2 Lipolytic methods for regional adiposity Lithera, Inc (US) 2013-04-16 US disclosed
US-20120046256-A1 Lipolytic Methods for Regional Adiposity Comprising Salmeterol or Formoterol LITHERA, INC. (US) 2012-02-23 US disclosed
US-20110105446-A1 Sustained Release Enhanced Lipolytic Formulation for Regional Adipose Tissue Treatment LITHERA, INC. (US) 2011-05-05 US disclosed
US-7829554-B2 contacting a targeted fat deposit with a formulation comprising long acting beta-2 adrenergic receptor agonist selected from salmeterol, formoterol and a glucocorticosteroid (e.g. dexamethasone, prednisolone, fluticasone, budesonid), a carrier, a excipient formulated for injection LITHERA, INC. (US) 2010-11-09 US disclosed
US-20100137267-A1 FORMULATIONS FOR TREATMENT OF ADIPOSE TISSUE, CUTANEOUS TISSUE AND DISORDERS, AND MUSCULAR TISSUE NEOTHETICS, INC. 2010-06-03 US disclosed
US-20100119609-A1 METHODS, COMPOSITIONS, AND FORMULATIONS FOR THE TREATMENT OF THYROID EYE DISEASE NEOTHETICS, INC. 2010-05-13 US disclosed
US-20090317477-A1 COMBINATION OF DEHYDROEPIANDROSTERONE OR DEHYDROEPIANDROSTERONE-SULFATE WITH A GLUCOCORTICOSTEROID FOR TREATMENT OF ASTHMA, CHRONIC OBSTRUCTIVE PULMONARY DISEASE OR ALLERGIC RHINITIS EPIGENESIS PHARMACEUTICALS, LLC 2009-12-24 US disclosed
WO-2007011743-A2 SUSTAINED RELEASE ENHANCED LIPOLYTIC FORMULATION FOR REGIONAL ADIPOSE TISSUE TREATMENT LIPOTHERA, INC. (US) 2007-01-25 WO disclosed
US-20070014843-A1 contacting a targeted fat deposit with a formulation comprising long acting beta-2 adrenergic receptor agonist selected from salmeterol, formoterol and a glucocorticosteroid (e.g. dexamethasone, prednisolone, fluticasone, budesonid), a carrier, a excipient formulated for injection NEOTHETICS, INC. 2007-01-18 US disclosed
US-20070014843-A1 contacting a targeted fat deposit with a formulation comprising long acting beta-2 adrenergic receptor agonist selected from salmeterol, formoterol and a glucocorticosteroid (e.g. dexamethasone, prednisolone, fluticasone, budesonid), a carrier, a excipient formulated for injection NEOTHETICS, INC. 2007-01-18 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (8 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20160287611-A1 METHODS, COMPOSITIONS, AND FORMULATIONS FOR THE TREATMENT OF THYROID EYE DISEASE TSHR, TRHR, ADRB2 NR3C1 27/4885PGR 427/4885CYP3A4 2776/4885
US-20100119609-A1 METHODS, COMPOSITIONS, AND FORMULATIONS FOR THE TREATMENT OF THYROID EYE DISEASE TSHR, TRHR, ADRB2 NR3C1 27/4885PGR 427/4885CYP3A4 2776/4885
US-20070014843-A1 contacting a targeted fat deposit with a formulation comprising long acting beta-2 adrenergic receptor agonist selected from salmeterol, formoterol and a glucocorticosteroid (e.g. dexamethasone, prednisolone, fluticasone, budesonid), a carrier, a excipient formulated for injection ADRB2, NR3C2, ADRB1 NR3C1 8/4885PGR 305/4885CYP3A4 431/4885
US-20170266137-A1 LIPOLYTIC METHODS LIPE, LIPC, LIPA NR3C1 128/4885PGR 980/4885CYP3A4 1138/4885
US-20120046256-A1 Lipolytic Methods for Regional Adiposity Comprising Salmeterol or Formoterol ADRB2, LIPE, ADRB3 NR3C1 47/4885PGR 1043/4885CYP3A4 1364/4885
US-20100137267-A1 FORMULATIONS FOR TREATMENT OF ADIPOSE TISSUE, CUTANEOUS TISSUE AND DISORDERS, AND MUSCULAR TISSUE ADRB2, ADRA2C, ADRA2A NR3C1 17/4885PGR 574/4885CYP3A4 980/4885
US-20110105446-A1 Sustained Release Enhanced Lipolytic Formulation for Regional Adipose Tissue Treatment ADRB2, LIPE, ADRA2A NR3C1 32/4885PGR 416/4885CYP3A4 1399/4885
US-20090317477-A1 COMBINATION OF DEHYDROEPIANDROSTERONE OR DEHYDROEPIANDROSTERONE-SULFATE WITH A GLUCOCORTICOSTEROID FOR TREATMENT OF ASTHMA, CHRONIC OBSTRUCTIVE PULMONARY DISEASE OR ALLERGIC RHINITIS NR5A1, HSD11B2, HSD3B1 NR3C1 18/4885PGR 79/4885CYP3A4 1457/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.