Teprotide

Teprotide

SCHEMBL613590

CCC(C)[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H]1CCC(=O)N1)C(=O)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(=O)O

nearest known ligand 0.52

Full drug profile on Sugi Atlas →

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
▸ F13A1 P00488 2/20 0.52
▸ TGM2 P21980 2/20 0.52
▸ CXCR4 P61073 2/20 0.51
▸ APLNR P35414 2/20 0.50
▸ ABCC2 Q92887 1/20 0.49
▸ GNRHR P30968 1/20 0.49
▸ PTGS1 P23219 1/20 0.49
▸ CTSL P07711 2/20 0.48
▸ CTSS P25774 2/20 0.48
▸ CTSK P43235 2/20 0.48
▸ CTSH P09668 1/20 0.48
▸ CTNNB1 P35222 1/20 0.48
▸ IL23R Q5VWK5 1/20 0.48

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
Teprotide SCHEMBL11855843 1.00 F13A1 (0.52) F13A1TGM2CXCR4APLNRABCC2
Teprotide SCHEMBL8158703 0.97 CXCR4 (0.51) F13A1TGM2CXCR4APLNRABCC2
SCHEMBL11872216 0.96 GNRHR (0.50) F13A1TGM2CXCR4APLNRABCC2
SCHEMBL11867492 0.94 GNRHR (0.51) F13A1TGM2CXCR4APLNRABCC2
Teprotide SCHEMBL613757 0.92 GNRHR (0.57) F13A1TGM2APLNRABCC2GNRHR
SCHEMBL11863118 0.89 IL23R (0.51) F13A1TGM2CXCR4CTSLCTSS
SCHEMBL11863142 0.89 IL23R (0.51) F13A1TGM2CXCR4CTSLCTSS
SCHEMBL24120770 0.87 CXCR4 (0.55) CXCR4CTSLCTSSCTSKCTSH
SCHEMBL11865471 0.86 CXCR4 (0.46) F13A1TGM2CXCR4APLNRABCC2
SCHEMBL11872436 0.86 CASP1 (0.51) CXCR4CTSLCTSSCTSKCTSH

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 1618 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2023183932-A2 MONOBODIES BINDING TO INTERCELLULAR ADHESION MOLECULE 2 (ICAM-2) NEW YORK UNIVERSITY (US) 2023-09-28 — — WO claimed
EP-3485908-B1 THERAPEUTIC COMBINATION AND USE OF DLL4 ANTAGONIST ANTIBODIES AND ANTI-HYPERTENSIVE AGENTS MEREO BIOPHARMA 5 INC (US) 2021-08-18 — — EP claimed
EP-3544597-A1 THERAPIES FOR THE TREATMENT OF LIDOCAINE-INEFFECTIVE AND HYPOKALEMIC CONDITIONS Alkalidx, Inc. (US) 2019-10-02 — — EP claimed
EP-3072526-B1 THERAPEUTIC COMBINATION AND USE OF DLL4 ANTAGONIST ANTIBODIES AND ANTI-HYPERTENSIVE AGENTS ONCOMED PHARM INC (US) 2018-09-26 — — EP claimed
WO-2018098273-A1 THERAPIES FOR THE TREATMENT OF LIDOCAINE-INEFFECTIVE AND HYPOKALEMIC CONDITIONS ALKALIDX, INC. (US) 2018-05-31 — — WO claimed
US-9982042-B2 Therapeutic combination and methods of treatment with a DLL4 antagonist and an anti-hypertensive agent ONCOMED PHARMACEUTICALS, INC. (US) 2018-05-29 — — US claimed
US-20180118699-A1 SK AND IK CHANNEL AGONISTS FOR TREATMENT OF HEART FAILURE THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK 2018-05-03 — — US claimed
US-20170299598-A1 Methods and Monitoring of Treatment With A DLL4 Antagonist ONCOMED PHARMACEUTICALS, INC. 2017-10-19 — — US claimed
US-20170166632-A1 Therapeutic Combination and Methods of Treatment With A DLL4 Antagonist and an Anti-Hypertensive Agent ONCOMED PHARMACEUTICALS, INC. 2017-06-15 — — US claimed
US-9511139-B2 Therapeutic combination and methods of treatment with a DLL4 antagonist and an anti-hypertensive agent ONCOMED PHARMACEUTICALS, INC. (US) 2016-12-06 — — US claimed
WO-1991011999-A1 ANGIOTENSIN II ANTAGONISTS INCORPORATING A SUBSTITUTED BENZYL ELEMENT MERCK & CO., INC. (US) 1991-08-22 — — WO claimed
WO-1991012001-A1 ANGIOTENSIN II ANTAGONISTS INCORPORATING A SUBSTITUTED BENZYL ELEMENT MERCK & CO., INC. (US) 1991-08-22 — — WO claimed
EP-0419048-A2 Substituted pyrimidinones as angiotensin II antagonists MERCK & CO. INC. (US) 1991-03-27 — — EP claimed
EP-0412594-A2 Substituted triazolinones, triazolinethiones, and triazolinimines as angiotensin II antagonists MERCK & CO. INC. (US) 1991-02-13 — — EP claimed
EP-0411766-A1 Substituted quinazolinones as angiotensin II antagonists MERCK & CO. INC. (US) 1991-02-06 — — EP claimed
EP-0409332-A2 Substituted triazoles as angiotensin II antagonists MERCK & CO. INC. (US) 1991-01-23 — — EP claimed
EP-0407102-A1 Substituted imidazo-fused 5-membered ring heterocycles as angiotensin II antagonists MERCK & CO. INC. (US) 1991-01-09 — — EP claimed
EP-0400974-A2 Substituted imidazo-fused 6-membered heterocycles as angiotensin II antagonists MERCK & CO. INC. (US) 1990-12-05 — — EP claimed
EP-0401030-A2 Angiotensin II antagonists MERCK & CO. INC. (US) 1990-12-05 — — EP claimed
EP-0400835-A1 Substituted benzimidazoles as angiotensin II antagonists MERCK & CO. INC. (US) 1990-12-05 — — EP 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 (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-20180118699-A1 SK AND IK CHANNEL AGONISTS FOR TREATMENT OF HEART FAILURE KCNH2, KCNK5, KCNN3 F13A1 3653/4885TGM2 4510/4885CXCR4 1335/4885

“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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