Morpholine

Morpholine

SCHEMBL702116

C1COCCN1.NC(=S)[S-].[Na+]

nearest known ligand 0.55

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABCC8ACEADORA1ADORA2AADORA2BADORA3ALDH5A1ALOX5ALOX5APATP4AATP4BBRAFCA1CA12CA2CA4CYSLTR1DHFRDPEP1EDNRAEDNRBESR2F10FDPSFGF1GABBR1GABBR2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGARTGNRHRGSC1HMGCRIMPDH1IMPDH2KCNJ11LY96NOD2NR3C1NS3NS4ANS5bP2RY1P2RY12P2RY2P2RY4P2RY6PBP2XPDE3APDE3BPDE4APDE4BPDE4CPDE4DPDK1PDK2PDK3PDK4PPARGPPATPTGIRPTGS1PTGS2RAF1RYR1RYR3SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASERPINC1SLC12A1SLC12A3SYKTHRATHRBTLR3TLR4TLR9TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYMSVKORC1XDHblablaIMP-1blaOXA-33blaOXA-58blaT-3blaT-4blaT-5blaT-6dacAdacBdacCfolAfolPfolP1ftsIfusAgaggyrAgyrBmecAmrcAmrcBmrdApbp1apbp1bpbp2pbp2apbp2bpbp3pbp4pbpApbpBpbpCpbpFpolponBrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpoArpoBrpoCrpoZrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

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

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
CA1 known ✓ P00915 7/20 0.41
CA12 known ✓ O43570 6/20 0.41
CA2 known ✓ P00918 6/20 0.41
CA4 known ✓ P22748 1/20 0.30
MEN1 O00255 1/20 0.55
KMT2A Q03164 1/20 0.55
KDM4E B2RXH2 1/20 0.55
GAA P10253 1/20 0.55
CYP2C9 P11712 1/20 0.55
CA9 Q16790 6/20 0.41
SMN1; SMN2 Q16637 2/20 0.33
HTT P42858 1/20 0.33
LMNA P02545 1/20 0.32

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
Morpholine SCHEMBL29191392 0.97 MEN1 (0.52) MEN1KMT2AKDM4EGAACYP2C9
Morpholine SCHEMBL7987130 0.89 MEN1 (0.61) MEN1KMT2AKDM4EGAACYP2C9
Morpholine SCHEMBL497396 0.84 MEN1 (0.55) MEN1KMT2AKDM4EGAACYP2C9
Morpholine SCHEMBL10425540 0.82 MEN1 (0.52) MEN1KMT2AKDM4EGAACYP2C9
Piperazine SCHEMBL18091103 0.80 HIF1A (0.43) KDM4EGAACYP2C9CA1CA12
Morpholine SCHEMBL8009459 0.80
Morpholine SCHEMBL7554037 0.78 MEN1 (0.61) MEN1KMT2AKDM4EGAACYP2C9
Morpholine SCHEMBL2520893 0.78 KDM4E (0.61) MEN1KMT2AKDM4EGAACYP2C9
Piperazine SCHEMBL28520413 0.77 HIF1A (0.40) CA1CA12CA9CA2SMN1; SMN2
Morpholine SCHEMBL10379240 0.76

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4294576-B1 DITHIOCARBAMATE DEPRESSANTS, METHODS AND USES THEREOF IN FROTH FLOTATION MINERAL SEPARATION TESSENDERLO KERLEY INC (US) 2024-12-25 EP disclosed
US-20240149277-A1 DITHIOCARBAMATE DEPRESSANTS, METHODS AND USES THEREOF IN FROTH FLOTATION MINERAL SEPARATION TESSENDERLO KERLEY, INC. (US) 2024-05-09 US disclosed
CN-117861863-A Inhibitor of non-molybdenum sulfide ore and application of inhibitor in metal sulfide ore flotation separation 江西理工大学 2024-04-12 CN disclosed
EP-4294576-A1 DITHIOCARBAMATE DEPRESSANTS, METHODS AND USES THEREOF IN FROTH FLOTATION MINERAL SEPARATION Tessenderlo Kerley, Inc. (US) 2023-12-27 EP disclosed
WO-2022177872-A1 DITHIOCARBAMATE DEPRESSANTS, METHODS AND USES THEREOF IN FROTH FLOTATION MINERAL SEPARATION TESSENDERLO KERLEY, INC. (US) 2022-08-25 WO disclosed
US-8123982-B2 Dithiocarbamates provide improvement over tolyltriazole in inhibiting yellow metal corrosion AKZO NOBEL N.V. (NL) 2012-02-28 US disclosed
US-20050211957-A1 Sulfur based corrosion inhibitors AKZO NOBEL N.V. (NL) 2005-09-29 US disclosed
EP-1580301-A1 Sulfur based corrosion inhibitors National Starch and Chemical Investment Holding Corporation (US) 2005-09-28 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-20240149277-A1 DITHIOCARBAMATE DEPRESSANTS, METHODS AND USES THEREOF IN FROTH FLOTATION MINERAL SEPARATION ACMSD, AP2A1, CA3 CA1 7/4885CA12 342/4885CA2 18/4885

“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.