Nifedipine

Nifedipine

SCHEMBL1172946

COC(=O)C1=C(C)NC(C)=C(C(=O)OC)C1c1ccccc1[N+](=O)[O-].COC(=O)C1=C(C)NC(C)=C(C(=O)OC)C1c1ccccc1[N+](=O)[O-]

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

CACNA1CCACNA1DCACNA1FCACNA1S

The experimentally established mechanism targets of Nifedipine. 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
CACNA1C known ✓ Q13936 6/20 1.00
CACNA1F known ✓ O60840 2/20 1.00
CACNA1D known ✓ Q01668 2/20 1.00
CACNA1S known ✓ Q13698 2/20 1.00
ADORA3 P0DMS8 7/20 1.00
CYP1A2 P05177 6/20 1.00
CYP3A4 P08684 5/20 1.00
CYP2C9 P11712 5/20 1.00
CYP2C19 P33261 5/20 1.00
MAPT P10636 4/20 1.00
LMNA P02545 3/20 1.00
TSHR P16473 3/20 1.00
NFKB1 P19838 3/20 1.00
KMT2A Q03164 3/20 1.00
ABCC4 O15439 2/20 1.00
ABCB11 O95342 2/20 1.00
ADORA2A P29274 2/20 1.00
ADORA1 P30542 2/20 1.00
OPRM1 P35372 2/20 1.00
SCN1A P35498 2/20 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
Nifedipine SCHEMBL29349595 1.00 ADORA3 (1.00) ADORA3CYP1A2CACNA1CCYP3A4CYP2C9
Nifedipine SCHEMBL3968 1.00 ADORA3 (1.00) ADORA3CYP1A2CACNA1CCYP3A4CYP2C9
Nifedipine SCHEMBL5694031 0.99 ADORA3 (0.97) ADORA3CYP1A2CACNA1CCYP3A4CYP2C9
Nifedipine SCHEMBL27076589 0.99 ADORA3 (0.97) ADORA3CYP1A2CACNA1CCYP3A4CYP2C9
Nifedipine SCHEMBL27961697 0.99 ADORA3 (0.97) ADORA3CYP1A2CACNA1CCYP3A4CYP2C9
Nifedipine SCHEMBL8851397 0.99 ADORA3 (0.97) ADORA3CYP1A2CACNA1CCYP3A4CYP2C9
Nifedipine SCHEMBL3858071 0.99 ADORA3 (0.97) ADORA3CYP1A2CACNA1CCYP3A4CYP2C9
Nifedipine SCHEMBL27076587 0.99 ADORA3 (0.97) ADORA3CYP1A2CACNA1CCYP3A4CYP2C9
Nifedipine SCHEMBL8851402 0.99 ADORA3 (0.97) ADORA3CYP1A2CACNA1CCYP3A4CYP2C9
Nifedipine SCHEMBL9759614 0.96 ADORA3 (0.93) ADORA3CYP1A2CACNA1CCYP3A4CYP2C9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230256161-A9 Methods and Compositions for Treating a Disease Condition in a Subject Palo Alto Investors LP 2023-08-17 US disclosed
US-11382513-B2 Methods and compositions for treating a condition in a subject PALO ALTO INVESTORS (US) 2022-07-12 US disclosed
CN-113750069-B Nifedipine sustained release tablet and preparation method thereof 北京联嘉医药科技开发有限公司 2022-03-01 CN disclosed
US-20220047511-A1 HIGH PERFORMANCE EXCIPIENT COMPRISING CO-PROCESSED MICROCRYSTALLINE CELLULOSE AND SURFACE-REACTED CALCIUM CARBONATE OMYA INTERNATIONAL AG (CH) 2022-02-17 US disclosed
CN-113750069-A Nifedipine sustained release tablet and preparation method thereof 北京联嘉医药科技开发有限公司 2021-12-07 CN disclosed
US-20210121625-A1 Methods and Compositions for Treating a Disease Condition in a Subject YUN ANTHONY JOONKYOO (US) 2021-04-29 US disclosed
US-20200360271-A1 Methods and Compositions for Treating a Renal Disease Condition in a Subject Palo Alto Investors LP 2020-11-19 US disclosed
US-10716749-B2 Methods and compositions for treating a renal disease condition in a subject PALO ALTO INVESTORS (US) 2020-07-21 US disclosed
EP-1406594-B1 CONTROLLED AGGLOMERATION VELOXIS PHARMACEUTICALS AS (DK) 2019-06-05 EP disclosed
US-20180125419-A1 Methods and Compositions for Treating a Condition in a Subject PALO ALTO INVESTORS 2018-05-10 US disclosed
EP-1069918-A4 ENHANCEMENT OF CELLULAR GALLIUM UPTAKE UNIV OREGON HEALTH SCIENCES (US) 2002-02-20 EP disclosed
EP-1069918-A1 ENHANCEMENT OF CELLULAR GALLIUM UPTAKE Oregon Health Sciences University (US) 2001-01-24 EP disclosed
EP-0952770-A4 SYSTEM FOR RENDERING SUBSTANTIALLY NON-DISSOLUBLE BIO-AFFECTING AGENTS BIO-AVAILABLE FUISZ TECHNOLOGIES LTD (US) 1999-12-22 EP disclosed
EP-0952770-A1 SYSTEM FOR RENDERING SUBSTANTIALLY NON-DISSOLUBLE BIO-AFFECTING AGENTS BIO-AVAILABLE FUISZ TECHNOLOGIES LTD. (US) 1999-11-03 EP disclosed
WO-1999051277-A1 ENHANCEMENT OF CELLULAR GALLIUM UPTAKE OREGON HEALTH SCIENCES UNIVERSITY (US) 1999-10-14 WO disclosed
US-5958944-A TREATMENT OF CIRCULATORY DISEASES IN CORONARY, CEREBRAL, RENAL AND PERIPHERAL ARTERIES, AS A THERAPEUTIC AGENT FOR HYPERTENSION, ANGINA PECTORIS, AND RENAL AND PERIPHERAL CIRCULATION DISORDER, ANTIASTHMATIC AGENT YOSHITOMI PHARMACEUTICAL INDUSTRIES, LTD. (JP) 1999-09-28 US disclosed
WO-1997008950-A1 SYSTEM FOR RENDERING SUBSTANTIALLY NON-DISSOLUBLE BIO-AFFECTING AGENTS BIO-AVAILABLE FUISZ TECHNOLOGIES, LTD. (US) 1997-03-13 WO disclosed
US-5439687-A Having homogeneous matrix containing hydroxypropyl methyl cellulose, calcium antagonist, excipients SIEGFRIED PHARMA AG (CH) 1995-08-08 US disclosed
US-4954346-A Orally administrable nifedipine solution in a solid light resistant dosage form CIBA-GEIGY CORPORATION (US) 1990-09-04 US disclosed
US-4803081-A CONTAINING AN NONIONIC SOLUBILIZER AKTIEBOLAGET HASSLE (SE) 1989-02-07 US disclosed