Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL4338640

C[C@H]1CNCCN1.O=C(O)C(O)C(O)C(=O)O

nearest known ligand 0.40

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3CHRM1CHRM2CHRM3CHRM4ESR1ESR2GABRA1GABRB1GABRG2GBA1HRH1HTR1DHTR2AOPRD1OPRK1OPRM1SLC6A2SLC6A3TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8rplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

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

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GBA1 known ✓ P04062 1/20 0.39
GABRA1 known ✓ P14867 1/20 0.31
SLC6A2 known ✓ P23975 1/20 0.30
SLC6A3 known ✓ Q01959 1/20 0.30
TSHR P16473 3/20 0.40
NFKB1 P19838 1/20 0.32
CYP2C19 P33261 1/20 0.32
CPN1 P15169 2/20 0.32
CPB2 Q96IY4 2/20 0.32
SLC6A1 P30531 4/20 0.31
SLC6A11 P48066 3/20 0.31
SLC6A13 Q9NSD5 3/20 0.31
LMNA P02545 1/20 0.31
SMN1; SMN2 Q16637 1/20 0.31
GABRA5 P31644 2/20 0.31
GABRB2 P47870 2/20 0.31
SLC6A12 P48065 2/20 0.31
GABRR1 P24046 1/20 0.31
GABRA4 P48169 1/20 0.31
SLC6A4 P31645 1/20 0.30

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
Cadaverine Tartrate SCHEMBL4322353 1.00 TSHR (0.40) TSHRGBA1NFKB1CYP2C19CPN1
Cadaverine Tartrate SCHEMBL7749321 1.00 TSHR (0.40) TSHRGBA1NFKB1CYP2C19CPN1
Cadaverine Tartrate SCHEMBL7743890 1.00 TSHR (0.40) TSHRGBA1NFKB1CYP2C19CPN1
Bicarbonate SCHEMBL16669009 0.85 SLC6A1 (0.37) TSHRSLC6A1SLC6A11SLC6A13LMNA
Acetic Acid SCHEMBL28598584 0.83 SLC6A1 (0.35) TSHRSLC6A1SLC6A11SLC6A13LMNA
Oxalic Acid SCHEMBL9319555 0.83 SLC6A1 (0.35) TSHRSLC6A1SLC6A11SLC6A13LMNA
Acetic Acid SCHEMBL28060470 0.81 SLC6A1 (0.34) TSHRSLC6A1SLC6A11SLC6A13LMNA
Acetic Acid SCHEMBL28060411 0.81 SLC6A1 (0.34) TSHRSLC6A1SLC6A11SLC6A13LMNA
Acetic Acid SCHEMBL27717590 0.81 SLC6A1 (0.34) TSHRSLC6A1SLC6A11SLC6A13LMNA
Maleic Acid SCHEMBL27641950 0.78 TSHR (0.38) TSHRSLC6A1SLC6A11SLC6A13LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7569690-B2 Process for producing oxycarbonyl-substituted piperazine derivative TORAY FINE CHEMICALS CO., LTD. (JP) 2009-08-04 US disclosed
US-20060161003-A1 Process for producing oxycarbonyl-substituted piperazine derivative TORAY FINE CHEMICALS CO., LTD. (JP) 2006-07-20 US disclosed
EP-1548010-A1 PROCESS FOR PRODUCING OXYCARBONYL-SUBSTITUTED PIPERAZINE DERIVATIVE Toray Fine Chemicals Co., Ltd. (JP) 2005-06-29 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-20060161003-A1 Process for producing oxycarbonyl-substituted piperazine derivative DHPS, AQP4, OGFOD1 GBA1 898/4885GABRA1 3757/4885SLC6A2 4747/4885

“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.