Albuterol

Albuterol

SCHEMBL4434233

CC(C)(C)NCC(O)c1ccc(O)c(CO)c1.O=C(O)C(O)C(O)C(=O)O

nearest known ligand 0.82

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRB2

The experimentally established mechanism targets of Albuterol. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
ADRB2 known ✓ P07550 9/20 0.82
ADRB1 P08588 2/20 0.82
CYP1A2 P05177 2/20 0.82
TSHR P16473 2/20 0.82
NFKB1 P19838 2/20 0.82
HIF1A Q16665 2/20 0.82
CYP2D6 P10635 1/20 0.82
TDP1 Q9NUW8 3/20 0.81
PMP22 Q01453 1/20 0.77
KDM4E B2RXH2 2/20 0.55
HSD17B10 Q99714 2/20 0.55
SLC6A2 P23975 1/20 0.55
GAA P10253 1/20 0.55
MAPT P10636 1/20 0.55
THPO P40225 1/20 0.55
BLM P54132 1/20 0.55
SMN1; SMN2 Q16637 1/20 0.55
RXFP1 Q9HBX9 1/20 0.55

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
Levosalbutamol SCHEMBL31301062 1.00 ADRB2 (0.82) ADRB2ADRB1CYP1A2TSHRNFKB1
Levosalbutamol SCHEMBL29394399 1.00 ADRB2 (0.82) ADRB2ADRB1CYP1A2TSHRNFKB1
Levosalbutamol SCHEMBL1247104 1.00 ADRB2 (0.82) ADRB2ADRB1CYP1A2TSHRNFKB1
Albuterol SCHEMBL6838948 0.92 ADRB2 (0.87) ADRB2ADRB1CYP1A2TSHRNFKB1
Albuterol SCHEMBL122805 0.91 ADRB2 (1.00) ADRB2ADRB1CYP1A2TSHRNFKB1
Albuterol SCHEMBL2489838 0.91 ADRB2 (1.00) ADRB2ADRB1CYP1A2TSHRNFKB1
Levosalbutamol SCHEMBL4003 0.91 ADRB2 (1.00) ADRB2ADRB1CYP1A2TSHRNFKB1
Albuterol SCHEMBL4913 0.91 ADRB2 (1.00) ADRB2ADRB1CYP1A2TSHRNFKB1
Albuterol SCHEMBL121596 0.91 ADRB2 (1.00) ADRB2ADRB1CYP1A2TSHRNFKB1
(S)-Albuterol SCHEMBL29496690 0.91 ADRB2 (1.00) ADRB2ADRB1CYP1A2TSHRNFKB1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117919258-A Medicinal liquid for treating bronchial asthma and administration device thereof 周子栋 2024-04-26 CN claimed
CN-116392460-A Salbutamol aerosol 山东京卫制药有限公司 2023-07-07 CN claimed
CN-115463117-A Budesonide salbutamol compound aerosol inhalation suspension with high delivery efficiency and preparation method thereof 四川普锐特药业有限公司 2022-12-13 CN claimed
EP-2018162-A2 METHODS FOR THE DELIVERY OF A BETA2 AGONIST TO INDUCE BRONCHODILATION AND FORMULATIONS FOR USE IN THE SAME Tika Läkemedel AB (SE) 2009-01-28 EP claimed
US-20080020003-A1 Methods for the delivery of a beta2 agonist to induce bronchodilation and formulations for use in the same VERUS PHARMACEUTICALS, INC. (US) 2008-01-24 US claimed
WO-2007137204-A2 METHODS FOR THE DELIVERY OF A BETA2 AGONIST TO INDUCE BRONCHODILATION AND FORMULATIONS FOR USE IN THE SAME TIKA LÄKEMEDEL AB (SE) 2007-11-29 WO claimed
CN-1206205-C Process for preparing R-salbutamol tartrate CHENGDU ORGANIC CHEM INST (CN) 2005-06-15 CN claimed
CN-1382685-A Process for preparing R-salbutamol tartrate CHENGDU ORGANIC CHEM INST (CN) 2002-12-04 CN claimed
CN-117919258-A Medicinal liquid for treating bronchial asthma and administration device thereof 周子栋 2024-04-26 CN disclosed
CN-116392460-A Salbutamol aerosol 山东京卫制药有限公司 2023-07-07 CN disclosed
CN-115463117-A Budesonide salbutamol compound aerosol inhalation suspension with high delivery efficiency and preparation method thereof 四川普锐特药业有限公司 2022-12-13 CN disclosed
US-20210290568-A1 INHALABLE FORMULATION OF A SOLUTION CONTAINING LEVALBUTEROL TARTRATE Huang, Cai Gu (US) 2021-09-23 US disclosed
WO-2021188809-A1 INHALABLE FORMULATION OF A SOLUTION CONTAINING LEVALBUTEROL TARTRATE HUANG CAI GU (US) 2021-09-23 WO disclosed
US-RE43984-E1 Process for preparing isomers of salbutamol CIPLA LIMITED (IN) 2013-02-05 US disclosed
WO-2007137204-A2 METHODS FOR THE DELIVERY OF A BETA2 AGONIST TO INDUCE BRONCHODILATION AND FORMULATIONS FOR USE IN THE SAME TIKA LÄKEMEDEL AB (SE) 2007-11-29 WO disclosed
US-6995286-B2 Resolution of racemic mixture using tartaric acid CIPLA LIMITED (IN) 2006-02-07 US disclosed
EP-1349828-B1 PROCESS FOR PREPARING ISOMERS OF SALBUTAMOL CIPLA LTD (IN) 2005-03-16 EP disclosed
US-20040054215-A1 Process for preparing isomers of salbutamol CIPLA LIMITED (IN) 2004-03-18 US disclosed
EP-1349828-A1 PROCESS FOR PREPARING ISOMERS OF SALBUTAMOL Cipla Limited (IN) 2003-10-08 EP disclosed
WO-2002048090-A1 PROCESS FOR PREPARING ISOMERS OF SALBUTAMOL CIPLA LIMITED (IN) 2002-06-20 WO 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 (2 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-20040054215-A1 Process for preparing isomers of salbutamol ADRB1, ADRB2, ADRB3 ADRB2 2/4885ADRB1 1/4885CYP1A2 1134/4885
US-20210290568-A1 INHALABLE FORMULATION OF A SOLUTION CONTAINING LEVALBUTEROL TARTRATE NDUFB5, PDE12, NDUFB7 ADRB2 76/4885ADRB1 51/4885CYP1A2 1514/4885

“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.