Clobetasone Butyrate

Clobetasone Butyrate

SCHEMBL448850

CCCC(=O)OC1(C(=O)CCl)C(C)CC2C3CCC4=CC(=O)C=CC4(C)C3(F)C(=O)CC21C

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ LMNA P02545 4/20 1.00
▸ MAPT P10636 3/20 1.00
▸ SMN1; SMN2 Q16637 2/20 1.00
▸ NPSR1 Q6W5P4 2/20 1.00
▸ CYP3A4 P08684 6/20 0.69
▸ PGR P06401 6/20 0.69
▸ USP2 O75604 5/20 0.69
▸ NR3C1 P04150 5/20 0.69
▸ NR1I2 O75469 2/20 0.69
▸ CYP2D6 P10635 2/20 0.69
▸ CYP2C9 P11712 2/20 0.69
▸ MLNR O43193 1/20 0.69
▸ ABCB11 O95342 1/20 0.69
▸ CYP3A5 P20815 1/20 0.69
▸ PPARG P37231 1/20 0.69
▸ MEN1 O00255 1/20 0.63
▸ KMT2A Q03164 1/20 0.63
▸ ADORA3 P0DMS8 3/20 0.57
▸ DRD2 P14416 1/20 0.57
▸ OPRD1 P41143 1/20 0.57

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
Clobetasone Butyrate SCHEMBL11750078 1.00 LMNA (1.00) LMNAMAPTSMN1; SMN2NPSR1CYP3A4
Clobetasone Butyrate SCHEMBL36599 1.00 LMNA (1.00) LMNAMAPTSMN1; SMN2NPSR1CYP3A4
Clobetasone Butyrate SCHEMBL29410388 1.00 LMNA (1.00) LMNAMAPTSMN1; SMN2NPSR1CYP3A4
Clobetasone Butyrate SCHEMBL29572705 1.00 LMNA (1.00) LMNAMAPTSMN1; SMN2NPSR1CYP3A4
Clobetasone Butyrate SCHEMBL11124627 1.00 LMNA (1.00) LMNAMAPTSMN1; SMN2NPSR1CYP3A4
Clobetasone Butyrate SCHEMBL14339619 1.00 LMNA (1.00) LMNAMAPTSMN1; SMN2NPSR1CYP3A4
SCHEMBL732359 0.96 LMNA (0.92) LMNAMAPTSMN1; SMN2NPSR1CYP3A4
SCHEMBL568167 0.94 LMNA (0.88) LMNAMAPTSMN1; SMN2NPSR1CYP3A4
SCHEMBL28099304 0.94 LMNA (0.88) LMNAMAPTSMN1; SMN2NPSR1CYP3A4
SCHEMBL11748908 0.93 LMNA (0.87) LMNAMAPTSMN1; SMN2NPSR1CYP3A4

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 1993 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4255391-B1 LUMINOL FOR USE IN THE TREATMENT OF SEQUELAE OF A SARS-COV-2 INFECTION METRIOPHARM AG (CH) 2026-05-06 — — EP claimed
EP-4301343-B1 PHARMACEUTICAL COMPOSITIONS WITH REDUCED SIDE EFFECT AND METHODS OF USING THE SAME TLC BIOPHARMACEUTICALS INC (US) 2025-11-19 — — EP claimed
EP-4178579-B1 5-AMINO-2,3-DIHYDRO-1,4-PHTHALAZINEDIONE AS GLUCOCORTICOID-SPARING AGENT METRIOPHARM AG (CH) 2025-02-12 — — EP claimed
EP-3773563-B1 PRODRUGS OF FUSED-BICYCLIC C5AR ANTAGONISTS CHEMOCENTRYX INC (US) 2024-10-16 — — EP claimed
US-20240216286-A1 NANOSPHERE AND USE THEREOF CHANG GUNG UNIVERSITY (TW) 2024-07-04 — — US claimed
US-20240156839-A1 PHARMACEUTICAL COMPOSITIONS WITH REDUCED SIDE EFFECT AND METHODS OF USING THE SAME TLC BIOPHARMACEUTICALS, INC. 2024-05-16 — — US claimed
EP-3728203-B1 DIARYL SUBSTITUTED 6,5-FUSED RING COMPOUNDS AS C5aR INHIBITORS CHEMOCENTRYX INC (US) 2024-03-13 — — EP claimed
EP-4301343-A1 PHARMACEUTICAL COMPOSITIONS WITH REDUCED SIDE EFFECT AND METHODS OF USING THE SAME TLC Biopharmaceuticals, Inc. (US) 2024-01-10 — — EP claimed
WO-2023183932-A2 MONOBODIES BINDING TO INTERCELLULAR ADHESION MOLECULE 2 (ICAM-2) NEW YORK UNIVERSITY (US) 2023-09-28 — — WO claimed
US-20230241060-A1 GLUCOCORTICOID-SPARING AGENT METRIOPHARM AG (CH) 2023-08-03 — — US claimed
WO-2012068454-A2 NRF2 DEFICIENCY INFLUENCES SUSCEPTIBILITY TO STEROID RESISTANCE VIA HDAC2 REDUCTION UNIVERSITY OF ROCHESTER (US) 2012-05-24 — — WO claimed
WO-2011064661-A1 SMALL PYRIMIDINE DERIVATIVES AND METHODS OF USE THEREOF PROTEOLOGICS, LTD. (IL) 2011-06-03 — — WO claimed
WO-2011064657-A2 QUINAZOLIN-4(3A)-ONE DERIVATIVES AND METHODS OF USE THEREOF PROTEOLOGICS, LTD. (IL) 2011-06-03 — — WO claimed
US-20110130374-A1 Small Pyrimidine Derivatives and Methods of Use Thereof BIOSEARCH(2007) LTD. (IL) 2011-06-02 — — US claimed
US-20110129463-A1 Quinazolin-4(3A)-One Derivatives and Methods of Use Thereof PROTEOLOGICS, LTD. (IL) 2011-06-02 — — US claimed
US-20080206161-A1 QUIESCENT FOAMABLE COMPOSITIONS, STEROIDS, KITS AND USES THEREOF FOAMIX PHARMACEUTICALS LTD. (IL) 2008-08-28 — — US claimed
EP-1890679-A2 STEROID KIT AND FOAMABLE COMPOSITION AND USES THEREOF Foamix Ltd. (IL) 2008-02-27 — — EP claimed
WO-2007012977-A2 STEROID KIT AND FOAMABLE COMPOSITION AND USES THEREOF FOAMIX LTD (US) 2007-02-01 — — WO claimed
US-20060193789-A1 Surfacant, film forming agent, water, gas propellant; plant and animal extracts and oils; may include malathion FOAMIX LTD. (IL) 2006-08-31 — — US claimed
US-20060018937-A1 Steroid kit and foamable composition and uses thereof FOAMIX LTD. 2006-01-26 — — US claimed

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

For each of this compound's patents that has machine-readable text (4 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-20080206161-A1 QUIESCENT FOAMABLE COMPOSITIONS, STEROIDS, KITS AND USES THEREOF NR5A1, CYP17A1, LIPA LMNA 266/4885MAPT 4587/4885SMN1; SMN2 3037/4885
US-20110129463-A1 Quinazolin-4(3A)-One Derivatives and Methods of Use Thereof USP3, CUL3, UBQLN1 LMNA 2099/4885MAPT 1775/4885SMN1; SMN2 3546/4885
US-20110130374-A1 Small Pyrimidine Derivatives and Methods of Use Thereof TYMS, UPP1, DPYD LMNA 3820/4885MAPT 3063/4885SMN1; SMN2 4590/4885
US-20060018937-A1 Steroid kit and foamable composition and uses thereof KIT, GK, HSD17B7 LMNA 1235/4885MAPT 3575/4885SMN1; SMN2 3689/4885

“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.

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