Tert-Butylamine

Tert-Butylamine

SCHEMBL1739621

CC(C)(C)N.CC(C)c1nc(N(C)S(C)(=O)=O)nc(-c2ccc(F)cc2)c1C=CCC[C@@H](O)C(O)C(=O)O

nearest known ligand 0.60

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACEIDH1

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

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
HMGCR P04035 6/20 0.60
ALDH1A1 P00352 1/20 0.60
CYP3A4 P08684 1/20 0.60
PDE6D O43924 1/20 0.60
NR1I2 O75469 1/20 0.60
PDE4D Q08499 1/20 0.60
ABCC3 O15438 1/20 0.57
ABCC4 O15439 1/20 0.57
HDAC1 Q13547 1/20 0.56
HDAC2 Q92769 1/20 0.56
HDAC6 Q9UBN7 1/20 0.56

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
SCHEMBL18979238 0.97 HMGCR (0.64) HMGCRALDH1A1CYP3A4PDE6DNR1I2
SCHEMBL1740204 0.97 HMGCR (0.64) HMGCRALDH1A1CYP3A4PDE6DNR1I2
SCHEMBL1739611 0.96 HMGCR (0.63) HMGCRALDH1A1CYP3A4PDE6DNR1I2
SCHEMBL2684323 0.96 HMGCR (0.63) HMGCRALDH1A1CYP3A4PDE6DNR1I2
SCHEMBL1741831 0.96 HMGCR (0.63) HMGCRALDH1A1CYP3A4PDE6DNR1I2
SCHEMBL3885922 0.92 HMGCR (0.62) HMGCRALDH1A1CYP3A4PDE6DNR1I2
SCHEMBL3884325 0.91 HMGCR (0.61) HMGCRALDH1A1CYP3A4PDE6DNR1I2
SCHEMBL6789988 0.87 HMGCR (0.59) HMGCRALDH1A1CYP3A4PDE6DNR1I2
SCHEMBL3971716 0.87 HMGCR (0.58) HMGCRALDH1A1CYP3A4PDE6DNR1I2
SCHEMBL16401135 0.84 HMGCR (0.55) HMGCRALDH1A1CYP3A4PDE6DNR1I2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2483248-B1 CRYSTALLINE FORM I ROSUVASTATIN ZINC SALT EGIS GYÓGYSZERGYÁR ZRT (HU) 2016-07-20 EP disclosed
US-9321733-B2 Crystalline pharmaceutically active ingredients EGIS GYOGYSZERGYAR NYILVANOSAN MUKODO RESZVENYTARSASAG (HU) 2016-04-26 US disclosed
US-9023838-B2 Crystalline form I rosuvastatin zinc salt EGIS GYOGYSZERGYAR NYILVANOSAN MUEKOEDOE (HU) 2015-05-05 US disclosed
US-20130296353-A1 CRYSTALLINE PHARMACEUTICALLY ACTIVE INGREDIENTS EGIS Gyogyszergyar Nyilvanosan Mukodo Reszvenytar- sasag (HU) 2013-11-07 US disclosed
EP-2640710-A2 CRYSTALLINE PHARMACEUTICALLY ACTIVE INGREDIENTS Egis Gyógyszergyár Nyilvánosan Müködö Részvénytársaság (HU) 2013-09-25 EP disclosed
US-8507513-B2 Process for the preparation of rosuvastatin salts EGIS GYOGYSZERGYAR NYILVANOSAN MUEKOEDOE RESZVENYTARSASAG (HU) 2013-08-13 US disclosed
US-20120178729-A1 CRYSTALLINE FORM I ROSUVASTATIN ZINC SALT EGIS GYOGYSZERGYAR NYILVANOSAN MUEKOEDOE (HU) 2012-07-12 US disclosed
WO-2012066365-A2 CRYSTALLINE PHARMACEUTICALLY ACTIVE INGREDIENTS EGIS GYÓGYSZERGYÁR Nyilvánosan Müködö Részvénytársaság (HU) 2012-05-24 WO disclosed
US-20120116082-A1 PROCESS FOR THE PREPARATION OF ROSUVASTATIN SALTS EGIS GYOGYSZERGYAR NYILVANOSAN MUEKOEDOE RESZVENYTARSASAG (HU) 2012-05-10 US disclosed
EP-2389365-A1 PROCESS FOR THE PREPARATION OF ROSUVASTATIN SALTS Egis Gyógyszergyár Nyilvánosan Müködö (HU) 2011-11-30 EP disclosed
US-8040819-B2 Discovery and identification of upstream device characteristics for self-configuration of customer premises equipment CISCO TECHNOLOGY, INC. (US) 2011-10-18 US disclosed
WO-2010082072-A1 PROCESS FOR THE PREPARATION OF ROSUVASTATIN SALTS EGIS GYÓGYSZERGYÁR (HU) 2010-07-22 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 (3 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-20120116082-A1 PROCESS FOR THE PREPARATION OF ROSUVASTATIN SALTS TERT, SLC30A6, HMGCR HMGCR 3/4885ALDH1A1 2602/4885CYP3A4 427/4885
US-20120178729-A1 CRYSTALLINE FORM I ROSUVASTATIN ZINC SALT SLC39A11, PCSK9, SLC39A3 HMGCR 7/4885ALDH1A1 2875/4885CYP3A4 1043/4885
US-20130296353-A1 CRYSTALLINE PHARMACEUTICALLY ACTIVE INGREDIENTS PCSK9, SLC39A11, SLC10A1 HMGCR 5/4885ALDH1A1 2460/4885CYP3A4 345/4885

“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.