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140896-21-5

INDOLICIDIN is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 140896-21-5 Structure

  • Basic information

    1. Product Name: INDOLICIDIN
    2. Synonyms: H-ILE-LEU-PRO-TRP-LYS-TRP-PRO-TRP-TRP-PRO-TRP-ARG-ARG-NH2;ILPWKWPWWPWRR-NH2;ILE-LEU-PRO-TRP-LYS-TRP-PRO-TRP-TRP-PRO-TRP-ARG-ARG-NH2;INDOLICIDIN;IndolicidinIndolicid;42: PN: US7381704 SEQID: 42 claimed sequence;L-ArgininaMide,L-isoleucyl-L-leucyl-L-prolyl-L-tryptophyl-L-lysyl-L-tryptophyl-L-prolyl-L-tryptophyl-L-tryptophyl-L-prolyl-L-tryptophyl-L-arginyl-
    3. CAS NO:140896-21-5
    4. Molecular Formula: C100H132N26O13
    5. Molecular Weight: 1906.28
    6. EINECS: N/A
    7. Product Categories: Peptide
    8. Mol File: 140896-21-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: −20°C
    8. Solubility: N/A
    9. Water Solubility: Soluble in water (1 mg/ml).
    10. CAS DataBase Reference: INDOLICIDIN(CAS DataBase Reference)
    11. NIST Chemistry Reference: INDOLICIDIN(140896-21-5)
    12. EPA Substance Registry System: INDOLICIDIN(140896-21-5)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany: 3
    5. RTECS: NM1890250
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 140896-21-5(Hazardous Substances Data)

140896-21-5 Usage

Uses

Indolicidin shows potent antimicrobial activity in vitro against bacteria and fungi.

Check Digit Verification of cas no

The CAS Registry Mumber 140896-21-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,8,9 and 6 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 140896-21:
(8*1)+(7*4)+(6*0)+(5*8)+(4*9)+(3*6)+(2*2)+(1*1)=135
135 % 10 = 5
So 140896-21-5 is a valid CAS Registry Number.
InChI:InChI=1/C100H132N26O13/c1-5-57(4)85(102)95(136)123-79(45-56(2)3)96(137)124-42-20-36-82(124)92(133)118-76(46-58-51-110-68-28-11-6-23-63(58)68)89(130)116-74(33-16-17-39-101)88(129)121-80(49-61-54-113-71-31-14-9-26-66(61)71)97(138)125-43-21-38-84(125)94(135)120-78(48-60-53-112-70-30-13-8-25-65(60)70)91(132)122-81(50-62-55-114-72-32-15-10-27-67(62)72)98(139)126-44-22-37-83(126)93(134)119-77(47-59-52-111-69-29-12-7-24-64(59)69)90(131)117-75(35-19-41-109-100(106)107)87(128)115-73(86(103)127)34-18-40-108-99(104)105/h6-15,23-32,51-57,73-85,110-114H,5,16-22,33-50,101-102H2,1-4H3,(H2,103,127)(H,115,128)(H,116,130)(H,117,131)(H,118,133)(H,119,134)(H,120,135)(H,121,129)(H,122,132)(H,123,136)(H4,104,105,108)(H4,106,107,109)/t57-,73-,74-,75-,76-,77-,78-,79-,80-,81-,82-,83-,84-,85-/m0/s1

140896-21-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Indolicidin

1.2 Other means of identification

Product number -
Other names Isoleucyl-leucyl-prolyl-tryptophyl-lysyl-tryptophyl-prolyl-tryptophyl-tryptophyl-prolyl-tryptophyl-arginyl-argininamide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:140896-21-5 SDS

140896-21-5Downstream Products

140896-21-5Relevant articles and documents

Improved bioactivity of antimicrobial peptides by addition of amino-terminal copper and nickel (ATCUN) binding motifs

Libardo, M. Daben,Cervantes, Jorge L.,Salazar, Juan C.,Angeles-Boza, Alfredo M.

, p. 1892 - 1901 (2014/08/18)

Antimicrobial peptides (AMPs) are promising candidates to help circumvent antibiotic resistance, which is an increasing clinical problem. Amino-terminal copper and nickel (ATCUN) binding motifs are known to actively form reactive oxygen species (ROS) upon

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