Tirofiban

Tirofiban

SCHEMBL140366

CCCCS(=O)(=O)N[C@@H](Cc1ccc(OCCCCC2CCNCC2)cc1)C(=O)O.[Cl-].[H+]

nearest known ligand 0.96

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ITGA2BITGB3

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

Predicted protein targets (top 5)

geneUniProtsupporting neighboursconfidence
ITGB3 known ✓ P05106 20/20 0.96
ITGA2B known ✓ P08514 20/20 0.96
ITGAV P06756 2/20 0.96
CHRM2 P08172 1/20 0.96
SLC6A4 P31645 1/20 0.96

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
Tirofiban SCHEMBL41326 0.99 ITGB3 (0.95) ITGB3ITGA2BITGAVCHRM2SLC6A4
Tirofiban SCHEMBL3685 0.98 ITGB3 (1.00) ITGB3ITGA2BITGAVCHRM2SLC6A4
Tirofiban SCHEMBL17721319 0.98 ITGB3 (1.00) ITGB3ITGA2BITGAVCHRM2SLC6A4
Tirofiban SCHEMBL618214 0.98 ITGB3 (1.00) ITGB3ITGA2BITGAVCHRM2SLC6A4
Tirofiban SCHEMBL28858023 0.97 ITGB3 (0.98) ITGB3ITGA2BITGAVCHRM2SLC6A4
Tirofiban SCHEMBL155170 0.97 ITGB3 (0.98) ITGB3ITGA2BITGAVCHRM2SLC6A4
Tirofiban SCHEMBL41327 0.97 ITGB3 (0.98) ITGB3ITGA2BITGAVCHRM2SLC6A4
Tirofiban SCHEMBL7388934 0.96 ITGB3 (0.96) ITGB3ITGA2BITGAVCHRM2SLC6A4
Tirofiban SCHEMBL41325 0.96 ITGB3 (0.96) ITGB3ITGA2BITGAVCHRM2SLC6A4
SCHEMBL13873863 0.89 ITGB3 (0.83) ITGB3ITGA2BITGAVCHRM2SLC6A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115448871-B Preparation method of tirofiban hydrochloride 中国药科大学 2023-07-11 CN disclosed
CN-115448871-A Preparation method of tirofiban hydrochloride 中国药科大学 2022-12-09 CN disclosed
US-11291670-B2 Therapeutic approaches for treating Alzheimer disease and related disorders through a modulation of angiogenesis PHARNEXT (FR) 2022-04-05 US disclosed
US-10874644-B2 Therapeutic approaches for treating Alzheimer disease and related disorders through a modulation of synapse function PHARNEXT (FR) 2020-12-29 US disclosed
CN-111138349-A Synthesis method of tirofiban hydrochloride intermediate III 鲁南制药集团股份有限公司 2020-05-12 CN disclosed
EP-3560496-A1 COMBINATION COMPOSITIONS FOR TREATING ALZHEIMER DISEASE AND RELATED DISORDERS WITH ZONISAMIDE AND ACAMPROSATE Pharnext (FR) 2019-10-30 EP disclosed
US-20190298698-A1 THERAPEUTIC APPROACHES FOR TREATING ALZHEIMER DISEASE AND RELATED DISORDERS THROUGH A MODULATION OF SYNAPSE FUNCTION PHARNEXT (FR) 2019-10-03 US disclosed
EP-2285374-B1 COMBINATION COMPOSITIONS FOR TREATING ALZHEIMER DISEASE AND RELATED DISORDERS WITH ZONISAMIDE AND ACAMPROSATE PHARNEXT (FR) 2019-09-18 EP disclosed
US-10350195-B2 Therapeutic approaches for treating Alzheimer disease and related disorders through a modulation of synapse function PHARNEXT (FR) 2019-07-16 US disclosed
CN-104127434-B Use Zonisamide and the combination composition of Acamprosate treatment Alzheimer disease and associated conditions 法奈科斯公司 2017-10-13 CN disclosed
CN-1668283-A Pharmaceutical composition with improved dissolution TRANSFORM PHARMACEUTICALS INC (US) 2005-09-14 CN disclosed
CN-1658903-A Combinations of peroxisome proliferator-activated receptor (ppar) activator(s) and sterol absorption inhibitor(s) and treatments for vascular indications SCHERING CORP (US) 2005-08-24 CN disclosed
EP-1515703-A1 PHARMACEUTICAL COMPOSITIONS WITH IMPROVED DISSOLUTION Transform Pharmaceuticals, Inc. (US) 2005-03-23 EP disclosed
US-20050025791-A1 Pharmaceutical compositions with improved dissolution TRANSFORM PHARMACEUTICALS, INC. 2005-02-03 US disclosed
WO-2004061433-A1 PHARMACEUTICAL COMPOSITIONS WITH IMPROVED DISSOLUTION TRANSFORM PHARMACEUTICALS, INC. (US) 2004-07-22 WO disclosed
WO-2004026235-A2 PHARMACEUTICAL COMPOSITIONS WITH IMPROVED DISSOLUTION TRANSFORM PHARMACEUTICALS, INC. (US) 2004-04-01 WO disclosed
WO-2004000284-A1 PHARMACEUTICAL COMPOSITIONS WITH IMPROVED DISSOLUTION TRANSFORM PHARMACEUTICALS, INC. (US) 2003-12-31 WO disclosed
EP-1353694-A2 COMBINATIONS OF STEROL ABSORPTION INHIBITOR(S) WITH BLOOD MODIFIER(S) FOR TREATING VASCULAR CONDITIONS Schering Corporation (US) 2003-10-22 EP disclosed
US-20020147184-A1 Combinations of sterol absorption inhibitor(s) with blood modifier(s) for treating vascular conditions SCHERING CORPORATION 2002-10-10 US disclosed
WO-2002058734-A2 COMBINATIONS OF STEROL ABSORPTION INHIBITOR(S) WITH BLOOD MODIFIER(S) FOR TREATING VASCULAR CONDITIONS SCHERING CORPORATION (US) 2002-08-01 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-20050025791-A1 Pharmaceutical compositions with improved dissolution ABCG2, SI, SLC10A2 ITGB3 4814/4885ITGA2B 4822/4885ITGAV 4745/4885
US-20020147184-A1 Combinations of sterol absorption inhibitor(s) with blood modifier(s) for treating vascular conditions APOB, FABP2, CYP46A1 ITGB3 1980/4885ITGA2B 2036/4885ITGAV 1801/4885

“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.