Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL25220108

C[C@@H]1CC(C)(C)c2cccc(N)c21.O=C(O)C(O)C(O)C(=O)O

nearest known ligand 0.39

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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 8)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 1/20 0.39
MAPT P10636 1/20 0.39
LMNA P02545 1/20 0.33
HIF1A Q16665 1/20 0.33
KDM4E B2RXH2 1/20 0.33
CCR2 P41597 1/20 0.32
AKR1B1 P15121 1/20 0.31
NOTUM Q6P988 1/20 0.31

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 SCHEMBL30414533 1.00 ALDH1A1 (0.39) ALDH1A1MAPTLMNAHIF1AKDM4E
Cadaverine Tartrate SCHEMBL16774507 1.00 ALDH1A1 (0.39) ALDH1A1MAPTLMNAHIF1AKDM4E
Cadaverine Tartrate SCHEMBL28017624 1.00 ALDH1A1 (0.39) ALDH1A1MAPTLMNAHIF1AKDM4E
Cadaverine Tartrate SCHEMBL25197447 1.00 ALDH1A1 (0.39) ALDH1A1MAPTLMNAHIF1AKDM4E
Cadaverine Tartrate SCHEMBL25265489 0.99 ALDH1A1 (0.38) ALDH1A1MAPTLMNAHIF1AKDM4E
SCHEMBL25197298 0.89 ALDH1A1 (0.35) ALDH1A1MAPT
Cadaverine Tartrate SCHEMBL30197635 0.87 LMNA (0.32) LMNAHIF1AKDM4E
SCHEMBL8626918 0.85 ALDH1A1 (0.41) ALDH1A1MAPTLMNAKDM4E
SCHEMBL16991796 0.85 ALDH1A1 (0.41) ALDH1A1MAPTLMNAKDM4E
SCHEMBL2779868 0.85 ALDH1A1 (0.41) ALDH1A1MAPTLMNAKDM4E

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-20230257408-A1 METHOD FOR PRODUCING OPTICALLY ACTIVE COMPOUND SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2023-08-17 US disclosed
EP-4186882-A1 METHOD FOR PRODUCING OPTICALLY ACTIVE COMPOUND SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2023-05-31 EP disclosed
CN-115836041-A Process for producing optically active compound 住友化学株式会社 2023-03-21 CN 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-20230257408-A1 METHOD FOR PRODUCING OPTICALLY ACTIVE COMPOUND SIRT1, SIRT3, HCCS ALDH1A1 323/4885MAPT 3900/4885LMNA 3427/4885

“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.