SCHEMBL4638378

SCHEMBL4638378

c1ccc(-c2nnn(C(c3ccccc3)(c3ccccc3)c3ccccc3)n2)cc1

nearest known ligand 0.51

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 3/20 0.51
POLB P06746 1/20 0.51
RAB9A P51151 3/20 0.47
L3MBTL1 Q9Y468 2/20 0.47
HPGD P15428 1/20 0.46
NPC1 O15118 2/20 0.44
ATM Q13315 1/20 0.41
MAPK1 P28482 2/20 0.41
TSHR P16473 1/20 0.41
ALDH1A1 P00352 1/20 0.41
CYP1A2 P05177 1/20 0.41
CYP2D6 P10635 1/20 0.41
CYP2C19 P33261 1/20 0.41

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
SCHEMBL4148430 0.89 SMN1; SMN2 (0.43) SMN1; SMN2POLBRAB9AL3MBTL1HPGD
SCHEMBL9137872 0.89 SMN1; SMN2 (0.46) SMN1; SMN2POLBRAB9AL3MBTL1HPGD
SCHEMBL30743612 0.86 ABCG2 (0.55) SMN1; SMN2POLBRAB9AL3MBTL1HPGD
SCHEMBL4639478 0.85 SMN1; SMN2 (0.40) SMN1; SMN2POLBRAB9AL3MBTL1HPGD
SCHEMBL28770200 0.85 POLB (0.40) SMN1; SMN2POLBRAB9AL3MBTL1HPGD
SCHEMBL30676079 0.85 HPGD (0.45) SMN1; SMN2POLBRAB9AL3MBTL1HPGD
SCHEMBL5091164 0.85 POLB (0.43) SMN1; SMN2POLBRAB9AL3MBTL1HPGD
SCHEMBL4639604 0.85 RAB9A (0.42) SMN1; SMN2POLBRAB9AL3MBTL1HPGD
SCHEMBL9136967 0.85 POLB (0.46) SMN1; SMN2POLBRAB9AL3MBTL1HPGD
SCHEMBL6617494 0.85 LMNA (0.46) SMN1; SMN2POLBRAB9AL3MBTL1HPGD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0455423-B1 Ortho-lithiation process for the synthesis of 2-substituted 1-(tetrazol-5-yl) benzenes MERCK & CO INC (US) 1996-12-18 EP claimed
EP-0455423-A2 Ortho-lithiation process for the synthesis of 2-substituted 1-(tetrazol-5-yl) benzenes MERCK & CO. INC. (US) 1991-11-06 EP claimed
US-5039814-A Chemical intermediates for angiotensin antagonist MERCK & CO., INC. (US) 1991-08-13 US claimed
EP-1384717-B1 2-(2'-triphenylmethyl-2'H-tetrazol-5'-yl)phenylboronic acid intermediates for the synthesis of A II receptor antagonists DU PONT (US) 2008-05-14 EP disclosed
US-20070249839-A1 Process for the Preparation of Losartan Potassium Form I CADILA PHARMACEUTICALS LTD. (IN) 2007-10-25 US disclosed
US-20070249839-A1 Process for the Preparation of Losartan Potassium Form I CADILA PHARMACEUTICALS LTD. (IN) 2007-10-25 US disclosed
EP-1660463-A1 A PROCESS FOR THE PREPARATION OF PHENYLTETRAZOLE DERIVATIVES Dipharma S.p.A. (IT) 2006-05-31 EP disclosed
WO-2005014560-A1 A PROCESS FOR THE PREPARATION OF PHENYLTETRAZOLE DERIVATIVES DIPHARMA S.P.A. (IT) 2005-02-17 WO disclosed
EP-0754042-A4 TREATMENT OF ATHEROSCLEROSIS WITH ANGIOTENSIN II RECEPTOR BLOCKING IMIDAZOLES MERCK & CO INC (US) 2004-06-23 EP disclosed
EP-1384717-A2 Tetrazolylphenylboronic acid intermediates for the synthesis of A II receptor antagonists E.I. DUPONT DE NEMOURS AND COMPANY (US) 2004-01-28 EP disclosed
EP-1019048-B1 USE OF AN ANGIOTENSIN II RECEPTOR ANTAGONIST FOR THE PREPARATION OF DRUGS TO INCREASE THE SURVIVAL RATE OF RENAL TRANSPLANT PATIENTS MERCK SHARP DOHME ITALIA S P A (IT) 2004-01-21 EP disclosed
WO-1992016524-A1 BENZO-FUSED LACTAMS PROMOTE RELEASE OF GROWTH HORMONE MERCK & CO., INC. (US) 1992-10-01 WO disclosed
US-5130439-A Tetrazolylphenylboronic acid intermediates for the synthesis of AII receptor antagonists E.I. DU PONT DE NEMOURS AND COMPANY, A CORPORATION OF DELAWARE 1992-07-14 US disclosed
EP-0455423-A2 Ortho-lithiation process for the synthesis of 2-substituted 1-(tetrazol-5-yl) benzenes MERCK & CO. INC. (US) 1991-11-06 EP disclosed
WO-1991015209-A1 SUBSTITUTED PYRIMIDINES, PYRIMIDINONES AND PYRIDOPYRIMIDINES MERCK & CO., INC. (US) 1991-10-17 WO disclosed
US-5039814-A Chemical intermediates for angiotensin antagonist MERCK & CO., INC. (US) 1991-08-13 US disclosed
US-4874867-A Tetrazole intermediates to antihypertensive compounds E. I. DU PONT DE NEMOURS AND COMPANY (US) 1989-10-17 US disclosed
US-4870186-A Tetrazole intermediates to antihypertensive compounds E. I. DU PONT DE NEMOURS AND COMPANY (US) 1989-09-26 US disclosed
US-4820843-A Tetrazole intermediates to antihypertensive compounds E. I. DU PONT DE NEMOURS AND COMPANY (US) 1989-04-11 US disclosed
EP-0291969-A2 Tetrazole intermediates to antihypertensive compounds E.I. DU PONT DE NEMOURS AND COMPANY (US) 1988-11-23 EP 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-20070249839-A1 Process for the Preparation of Losartan Potassium Form I AGTR1, REN, AGT SMN1; SMN2 4434/4885POLB 3372/4885RAB9A 4174/4885

“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.