Amlodipine

Amlodipine

SCHEMBL3399451

CCOC(=O)C1=C(COCCN)NC(C)=C(C(=O)OC)[C@H]1c1ccccc1Cl.O=C(O)C(O)C(O)C(=O)O

nearest known ligand 0.88

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

CACNA1CCACNA1DCACNA1FCACNA1S

The experimentally established mechanism targets of Amlodipine. 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 1/20 0.88
TBXA2R P21731 3/20 0.88
ADRA1A P35348 3/20 0.88
SLC6A3 Q01959 3/20 0.88
ADORA3 P0DMS8 3/20 0.88
ABCB11 O95342 3/20 0.88
HTR1A P08908 2/20 0.88
ADRA2A P08913 2/20 0.88
CHRM1 P11229 2/20 0.88
DRD1 P21728 2/20 0.88
SLC6A2 P23975 2/20 0.88
OPRM1 P35372 2/20 0.88
DRD3 P35462 2/20 0.88
KCNH2 Q12809 2/20 0.88
ABCB1 P08183 2/20 0.88
ADRB3 P13945 2/20 0.88
OPRK1 P41145 2/20 0.88
SCN5A Q14524 2/20 0.88
KCNK2 O95069 1/20 0.88
ADRB2 P07550 1/20 0.88

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
Amlodipine SCHEMBL5182627 1.00 TBXA2R (0.88) TBXA2RADRA1ASLC6A3ADORA3ABCB11
Levamlodipine SCHEMBL3403387 1.00 TBXA2R (0.88) TBXA2RADRA1ASLC6A3ADORA3ABCB11
Levamlodipine SCHEMBL3225344 0.99 TBXA2R (0.86) TBXA2RADRA1ASLC6A3ADORA3ABCB11
Amlodipine SCHEMBL2762990 0.96 TBXA2R (0.81) TBXA2RADRA1ASLC6A3ADORA3ABCB11
Amlodipine SCHEMBL8176202 0.96 ADRA1A (0.81) TBXA2RADRA1ASLC6A3ADORA3ABCB11
Amlodipine SCHEMBL6650712 0.95 TBXA2R (0.98) TBXA2RADRA1ASLC6A3ADORA3ABCB11
SCHEMBL13097922 0.94 TBXA2R (1.00) TBXA2RADRA1ASLC6A3ADORA3ABCB11
Amlodipine SCHEMBL26478 0.94 TBXA2R (1.00) TBXA2RADRA1ASLC6A3ADORA3ABCB11
Amlodipine SCHEMBL1816641 0.94 TBXA2R (1.00) TBXA2RADRA1ASLC6A3ADORA3ABCB11
Levamlodipine SCHEMBL30994756 0.94 TBXA2R (1.00) TBXA2RADRA1ASLC6A3ADORA3ABCB11

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7678921-B2 Method for the enantiomoeric separation of optical active amlodipine Shijiazhuang Pharmaceutical Group Ouyl Pharma. Co., Ltd. (CN) 2010-03-16 US claimed
US-20070093661-A1 Method for the enantiomoeric separation of optical active amlodipine SHIJIAZHUANG PHARMACEUTICAL GROUP OUYL PHAMA CO., LTD (CN) 2007-04-26 US claimed
US-7678921-B2 Method for the enantiomoeric separation of optical active amlodipine Shijiazhuang Pharmaceutical Group Ouyl Pharma. Co., Ltd. (CN) 2010-03-16 US disclosed
US-20070093661-A1 Method for the enantiomoeric separation of optical active amlodipine SHIJIAZHUANG PHARMACEUTICAL GROUP OUYL PHAMA CO., LTD (CN) 2007-04-26 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 (1 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-20070093661-A1 Method for the enantiomoeric separation of optical active amlodipine TMCO1, CACNA1C, CACNA1H CACNA1C 2/4885TBXA2R 1149/4885ADRA1A 387/4885

“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.